Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

de Boer, Elke
Ockeloen, Charlotte W.
Matalonga, Leslie
Horvath, Rita
Rodenburg, Richard J.
Coenen, Marieke J.H.
Janssen, Mirian
Henssen, Dylan
Gilissen, Christian
Steyaert, Wouter
Paramonov, Ida
Trimouille, Aurélien
Kleefstra, Tjitske
Verloes, Alain
Vissers, Lisenka E. L. M.

Open link

Publication date

September 2021

DOI

10.1038/s41431-021-00937-3

Publisher

Springer Science and Business Media LLC

Abstract

In the original publication of the article, consortium author lists were missing in the article. The details are as below

Extracted data

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

de Boer, Elke
Ockeloen, Charlotte W.
Matalonga, Leslie
Horvath, Rita
Rodenburg, Richard J.
Coenen, Marieke J.H.
Janssen, Mirian
Henssen, Dylan
Gilissen, Christian
Steyaert, Wouter
Paramonov, Ida
Trimouille, Aurélien
Kleefstra, Tjitske
Verloes, Alain
Vissers, Lisenka E. L. M.

Open link

Publication date

September 2021

DOI

10.1038/s41431-021-00937-3

Publisher

Springer Science and Business Media LLC

Abstract

In the original publication of the article, consortium author lists were missing in the article. The details are as below

Extracted data

Jaber Lyahyai
Bouchra Ouled Amar Bencheikh
Siham C. Elalaoui
Maria Mansouri
Lamia Boualla
Alexandre DIonne-Laporte
Dan Spiegelman
Patrick A. Dion
Patrick Cossette
Guy A. Rouleau
Abdelaziz Sefiani

April 2018

After publication of the original article [1] it was brought to our attention that author Bouchra Ou...

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

van Rheenen, W.
van der Spek, R.A.A.
Bakker, M.K.
van Vugt, J.J.F.A.
Hop, P.J.
Zwamborn, R.A.J.
de Klein, N.
Westra, H-J
Bakker, O.B.
Deelen, P.
Shireby, G.
Hannon, E.
Moisse, M.
Baird, D.
Restuadi, R.
Dolzhenko, E.
Dekker, A.M.
Gawor, K.
Westeneng, H-J
Tazelaar, G.H.P.
van Eijk, K.R.
Kooyman, M.
Byrne, R.P.
Doherty, M.
Heverin, M.
Al Khleifat, A.
Iacoangeli, A.
Shatunov, A.
Ticozzi, N.
Cooper-Knock, J.
Smith, B.N.
Gromicho, M.
Chandran, S.
Pal, S.
Morrison, K.E.
Shaw, P.J.
Hardy, J.
Orrell, R.W.
Sendtner, M.
Meyer, T.
Başak, N.
van der Kooi, A.J.
Ratti, A.
Fogh, I.
Gellera, C.
Lauria, G.
Corti, S.
Cereda, C.
Sproviero, D.
D’alfonso, S.
Sorarù, G.
Siciliano, G.
Filosto, M.
Padovani, A.
Chiò, A.
Calvo, A.
Moglia, C.
Brunetti, M.
Canosa, A.
Grassano, M.
Beghi, E.
Pupillo, E.
Logroscino, G.
Nefussy, B.
Osmanovic, A.
Nordin, A.
Lerner, Y.
Zabari, M.
Gotkine, M.
Baloh, R.H.
Bell, S.
Vourc’h, P.
Corcia, P.
Couratier, P.
Millecamps, S.
Meininger, V.
Salachas, F.
Mora Pardina, J.S.
Assialioui, A.
Rojas-García, R.
Dion, P.A.
Ross, J.P.
Ludolph, A.C.
Weishaupt, J.H.
Brenner, D.
Freischmidt, A.
Bensimon, G.
Brice, A.
Durr, A.
Payan, C.A.M.
Saker-Delye, S.
Wood, N.W.
Topp, S.
Rademakers, R.
Tittmann, L.
Lieb, W.
Franke, A.
Ripke, S.
Braun, A.
Kraft, J.
Whiteman, D.C.
Olsen, C.M.
Uitterlinden, A.G.
Hofman, A.
Rietschel, M.
Cichon, S.
Nöthen, M.M.
Amouyel, P.
Comi, G.
Riva, N.
Lunetta, C.
Gerardi, F.
Cotelli, M.S.
Rinaldi, F.
Chiveri, L.
Guaita, M.C.
Perrone, P.
Ceroni, M.
Diamanti, L.
Ferrarese, C.
Tremolizzo, L.
Delodovici, M.L.
Bono, G.
Canosa, A.
Manera, U.
Vasta, R.
Bombaci, A.
Casale, F.
Fuda, G.
Salamone, P.
Iazzolino, B.
Peotta, L.
Cugnasco, P.
De Marco, G.
Torrieri, M.C.
Palumbo, F.
Gallone, S.
Barberis, M.
Sbaiz, L.
Gentile, S.
Mauro, A.
Mazzini, L.
De Marchi, F.
Corrado, L.
D’Alfonso, S.
Bertolotto, A.
Gionco, M.
Leotta, D.
Odddenino, E.
Imperiale, D.
Cavallo, R.
Pignatta, P.
De Mattei, M.
Geda, C.
Papurello, D.M.
Gusmaroli, G.
Comi, C.
Labate, C.
Ruiz, L.
Ferrandi, D.
Rota, E.
Aguggia, M.
Di Vito, N.
Meineri, P.
Ghiglione, P.
Launaro, N.
Dotta, M.
Di Sapio, A.
Giardini, G.
Tiloca, C.
Peverelli, S.
Taroni, F.
Pensato, V.
Castellotti, B.
Comi, G.P.
Del Bo, R.
Ceroni, M.
Gagliardi, S.
Corrado, L.
Mazzini, L.
Raggi, F.
Simoncini, C.
Lo Gerfo, A.
Inghilleri, M.
Ferlini, A.
Simone, I.L.
Passarella, B.
Guerra, V.
Zoccolella, S.
Nozzoli, C.
Mundi, C.
Leone, M.
Zarrelli, M.
Tamma, F.
Valluzzi, F.
Calabrese, G.
Boero, G.
Rini, A.
Traynor, B.J.
Singleton, A.B.
Mitne Neto, M.
Cauchi, R.J.
Ophoff, R.A.
Wiedau-Pazos, M.
Lomen-Hoerth, C.
van Deerlin, V.M.
Grosskreutz, J.
Roediger, A.
Gaur, N.
Jörk, A.
Barthel, T.
Theele, E.
Ilse, B.
Stubendorff, B.
Witte, O.W.
Steinbach, R.
Hübner, C.A.
Graff, C.
Brylev, L.
Fominykh, V.
Demeshonok, V.
Ataulina, A.
Rogelj, B.
Koritnik, B.
Zidar, J.
Ravnik-Glavač, M.
Glavač, D.
Stević, Z.
Drory, V.
Povedano, M.
Blair, I.P.
Kiernan, M.C.
Benyamin, B.
Henderson, R.D.
Furlong, S.
Mathers, S.
McCombe, P.A.
Needham, M.
Ngo, S.T.
Nicholson, G.A.
Pamphlett, R.
Rowe, D.B.
Steyn, F.J.
Williams, K.L.
Mather, K.A.
Sachdev, P.S.
Henders, A.K.
Wallace, L.
de Carvalho, M.
Pinto, S.
Petri, S.
Weber, M.
Rouleau, G.A.
Silani, V.
Curtis, C.J.
Breen, G.
Glass, J.D.
Brown, R.H.
Landers, J.E.
Shaw, C.E.
Andersen, P.M.
Groen, E.J.N.
van Es, M.A.
Pasterkamp, R.J.
Fan, D.
Garton, F.C.
McRae, A.F.
Davey Smith, G.
Gaunt, T.R.
Eberle, M.A.
Mill, J.
McLaughlin, R.L.
Hardiman, O.
Kenna, K.P.
Wray, N.R.
Tsai, E.
Runz, H.
Franke, L.
Al-Chalabi, A.
Van Damme, P.
van den Berg, L.H.
Veldink, J.H.

January 2022

Correction to: Nature Genetics https://doi.org/10.1038/s41588-021-00973-1, published online 6 Decemb...

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

de Boer E.
Ockeloen C. W.
Matalonga L.
Horvath R.
Cohen E.
Cuesta I.
Danis D.
Denomme-Pichon A. -S.
Duffourd Y.
Gilissen C.
Johari M.
Laurie S.
Li S.
Matalonga L.
Nelson I.
Peters S.
Paramonov I.
Prasanth S.
Robinson P.
Sablauskas K.
Savarese M.
Steyaert W.
Topf A.
van der Velde J. K.
Vitobello A.
Rodenburg R. J.
Coenen M. J. H.
Janssen M.
Henssen D.
Gilissen C.
Steyaert W.
Paramonov I.
Banka S.
Benetti E.
Casari G.
Ciolfi A.
Clayton-Smith J.
Dallapiccola B.
de Boer E.
Faivre L.
Haack T. B.
Hammarsjo A.
Havlovicova M.
Hoischen A.
Hugon A.
Jackson A.
Kleefstra T.
Lindstrand A.
Lopez-Martin E.
Macek M.
Nigro V.
Nordgren A.
Pettersson M.
Pinelli M.
Pizzi S.
Posada M.
Radio F. C.
Renieri A.
Rooryck C.
Ryba L.
Schwarz M.
Tartaglia M.
Thauvin C.
Torella A.
Verloes A.
Vissers L.
Vyshka K.
Zurek B.
Trimouille A.
Kleefstra T.
Verloes A.
Vissers L. E. L. M.

January 2021

In the original publication of the article, consortium author lists were missing in the article. The...

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Schüle, Rebecca
Timmann, Dagmar
Erasmus, Corrie E.
Reichbauer, Jennifer
Wayand, Melanie
van de Warrenburg, Bart
Schöls, Ludger
Wilke, Carlo
Bevot, Andrea
Zuchner, Stephan
Beltran, Sergi
Laurie, Steven
Matalonga, Leslie
Graessner, Holm
Synofzik, Matthis

September 2021

In the original publication of the article, consortium author lists were missing in the article

Author Correction: Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (Nature Medicine, (2020), 26, 10, (1549-1556), 10.1038/s41591-020-1008-z)

Bernard, Elsa
Nannya, Yasuhito
Hasserjian, Robert P.
Devlin, Sean M.
Tuechler, Heinz
Medina-Martinez, Juan S.
Yoshizato, Tetsuichi
Shiozawa, Yusuke
Saiki, Ryunosuke
Malcovati, Luca
Levine, Max F.
Arango, Juan E.
Zhou, Yangyu
Solé, Francesc
Cargo, Catherine A.
Haase, Detlef
Creignou, Maria
Germing, Ulrich
Zhang, Yanming
Gundem, Gunes
Sarian, Araxe
van de Loosdrecht, Arjan A.
Jädersten, Martin
Tobiasson, Magnus
Kosmider, Olivier
Follo, Matilde Y.
Thol, Felicitas
Pinheiro, Ronald F.
Santini, Valeria
Kotsianidis, Ioannis
Boultwood, Jacqueline
Santos, Fabio P. S.
Schanz, Julie
Kasahara, Senji
Ishikawa, Takayuki
Tsurumi, Hisashi
Takaori-Kondo, Akifumi
Kiguchi, Toru
Polprasert, Chantana
Bennett, John M.
Klimek, Virginia M.
Savona, Michael R.
Belickova, Monika
Ganster, Christina
Palomo, Laura
Sanz, Guillermo
Ades, Lionel
Della Porta, Matteo Giovanni
Elias, Harold K.
Smith, Alexandra G.
Werner, Yesenia
Patel, Minal
Viale, Agnès
Vanness, Katelynd
Neuberg, Donna S.
Stevenson, Kristen E.
Menghrajani, Kamal
Bolton, Kelly L.
Fenaux, Pierre
Pellagatti, Andrea
Platzbecker, Uwe
Heuser, Michael
Valent, Peter
Chiba, Shigeru
Miyazaki, Yasushi
Finelli, Carlo
Voso, Maria Teresa
Shih, Lee-Yung
Fontenay, Michaela
Jansen, Joop H.
Cervera, José
Atsuta, Yoshiko
Gattermann, Norbert
Ebert, Benjamin L.
Bejar, Rafael
Greenberg, Peter L.
Cazzola, Mario
Hellström-Lindberg, Eva
Ogawa, Seishi
Papaemmanuil, Elli

May 2021

In the version of this article initially published, one name (Harold K. Elias) was omitted from the ...

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific Reports (2017) DOI: 10.1038/s41598-017-09320-z)

Taskesen, E
Mishra, A
van der Sluis, S
Ferrari, R
Veldink, J H
van Es, M A
Smit, A B
Posthuma, D
Pijnenburg, Y
Hernandez, DG
Nalls. MA
Rohrer JD
Ramasamy, A
Kwok, JBJ
Dobson-Stone, C
Schofield, PR
Halliday, GM
Hodges, JR
Piguet, O
Bartley, L
Thompson, E
Haan, E
Hernández, I
Ruiz, A
Boada, M
Borroni, B
Padovani, A
Cruchaga, C
Cairns, NJ
Benussi, L
Binetti G
Ghidoni, R
Forloni, G
Albani, D
Galimberti, D
Fenoglio, C
Serp
Wassermann EM
Baborie A
Jaros E
Tierney MC
Pastor P
Razquin C
Ortega-Cubero S
Alonso E
Perneczky R
Diehl-Schmid J
Alexopoulos P
Kurz A
Rainero I
Rubino E
Pinessi L
Rogaeva E
George-Hyslop PS
Rossi G
Tagliavini F
Giaccone G
Rowe JB
Schlachetzki JCM
Uphill J
Collinge J
Mead S
Danek A
Van Deerlin VM
Grossman M
Trojanowski JQ
van der Zee J
Van Broeckhoven C
Cappa SF
Leber I
Hannequin D
Golfier V
Vercelletto M
Brice A
Nacmias B
Sorbi S
Bagnoli S
Piaceri I
Nielsen JE
Hjermind LE
Riemenschneider M
Mayhaus M
Ibach B
Gasparoni G
Pichler S
Gu W
Rossor MN
Fox NC
Warren JD
Spillantini MG
Morris HR
Rizzu P
Heutink P
Snowden JS
Rollinson S
Richardson A
Gerhard A
Bruni AC
Maletta R
Frangipane F
Cupidi C
Bernardi L
Anfossi M
Gallo M
Conidi ME
Smirne N
Rademakers R
Baker M
Dickson DW
Graff-Radford NR
Petersen RC
Knopman D
Josephs KA
Boeve BF
Parisi JE
Seeley WW
Miller BL
Karydas AM
Rosen H
van Swieten JC
Dopper EGP
Seelaar H
Scheltens P
Logroscino G
Capozzo R
Novelli V
Puca AA
Franceschi M
Postiglione A
Milan G
Sorrentino P
Kristiansen M
Chiang HH
Graff C
Pasquier F
Rollin A
Deramecourt V
Lebouvier T
Kapogiannis D
Ferrucci L
Pickering-Brown S
Singleton AB
Hardy J
Momeni P.

January 2018

International FTD-Genomics Consortium was omitted from the author list in the original version of th...

Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

Nizon, Mathilde
Laugel, Vincent
Flanigan, Kevin
Pastore, Matthew
Waldrop, Megan
Rosenfeld, Jill
Marom, Ronit
Xiao, Rui
Gerard, Amanda
Pichon, Olivier
Le Caignec, Cédric
Gérard, Marion
Dieterich, Klaus
Truitt Cho, Megan
Mcwalter, Kirsty
Hiatt, Susan
Thompson, Michelle
Bézieau, Stéphane
Wadley, Alexandrea
Wierenga, Klaas
Egly, Jean-Marc
Isidor, Bertrand

November 2019

International audienceIn the Acknowledgements section of the paper the authors neglected to mention ...

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (Molecular Psychiatry, (2018), 10.1038/s41380-018-0112-7)

Bis, J.C. (Joshua)
Jian, X. (Xueqiu)
Kunkle, B.W. (Brian W.)
Chen, Y. (Yuning)
Hamilton-Nelson, K.L. (Kara L.)
Bush, W.S. (William S.)
Salerno, W.J. (William J.)
Lancour, D. (Daniel)
Ma, Y. (Yiyi)
Renton, A. (Alan)
Marcora, E. (Edoardo)
Farrell, J.J. (John J.)
Zhao, Y. (Yi)
Qu, L. (Liming)
Ahmad, S. (Shahzad)
Amin, N. (Najaf)
Amouyel, P. (Philippe)
Beecham, G.W.
Below, J.E. (Jennifer E.)
Campion, D. (Dominique)
Cantwell, L.B. (Laura B.)
Charbonnier, C. (Camille)
Chung, J. (Jaeyoon)
Crane, P.K. (Paul K.)
Crane, L.M.A.
Cupples, L.A. (L. Adrienne)
Dartigues, J.-F.
Debette, S. (Stéphanie)
Deleuze, J.-F. (Jean-François)
Fulton, L. (Lucinda)
Gabriel, S.B. (Stacey)
Genin, E. (Emmanuelle)
Gibbs, R.A. (Richard)
Goate, A. (Alison)
Grenier-Boley, B. (Benjamin)
Gupta, N. (Namrata)
Haines, J.L. (Jonathan)
Havulinna, A.S. (Aki)
Helisalmi, S. (Seppo)
Hiltunen, M. (Mikko)
Howrigan, D.P. (Daniel P.)
Ikram, M.A. (Arfan)
Kaprio, J. (Jaakko)
Konrad, J. (Jan)
Kuzma, A. (Amanda)
Lander, E.S. (Eric)
Lathrop, M. (Mark)
Lehtimäki, T. (Terho)
Lin, H. (Honghuang)
Mattila, K. (Kari)
Mayeux, R. (Richard)
Muzny, D. (Donna)
Nasser, W. (Waleed)
Neale, B.M. (Benjamin)
Nho, K. (Kwangsik)
Nicolas, G. (Gaël)
Patel, D. (Devanshi)
Kunkle, B. (Brian)
Perola, M. (Markus)
Psaty, B.M. (Bruce)
Quenez, O. (Olivier)
Rajabli, F. (Farid)
Redon, R. (Richard)
Reitz, C. (Christiane)
Remes, A. (Anne)
Salomaa, V. (Veikko)
Sarnowski, C.
Schmidt, H. (Helena)
Schmidt, M. (Michael)
Schmidt, R. (Reinhold)
Soininen, H. (H.)
Thornton, T.A. (Timothy A.)
Tosto, G. (G.)
Tzourio, C. (Christophe)
Lee, S.J. (Sven) van der
Duijn, C.M. (Cornelia) van
Valladares, O. (Otto)
Vardarajan, B.N. (Badri)
Wang, L.S. (Li-San)
Wang, W. (Weixin)
Wijsman, E. (Ellen)
Wilson, R.K. (Richard K.)
Witten, D. (Daniela)
Worley, K.C. (Kim C.)
Zhang, X. (Xiaoling)
Bellenguez, C. (Céline)
Lambert, J.-C. (J.)
Kurki, M.I. (Mitja I.)
Palotie, A. (Aarno)
Daly, M.J. (Mark)
Boerwinkle, E.A. (Eric)
Lunetta, K.L. (Kathryn)
DeStefano, A.L. (Anita)
Amin, N. (Najaf)
Martin, E.R.
Schellenberg, G.D. (Gerard)
Seshadri, S. (Sudha)
Naj, A.C. (Adam C.)
Fornage, M. (Myriam)
Farrer, L.A. (Lindsay)

January 2019

Following publication, the authors noticed that ‘Laura Cantwell’, ‘Otto Valladares’, and ‘Li-San Wan...

Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders (Genetics in Medicine, (2021), 10.1038/s41436-020-01096-4)

Sadikovic, Bekim
Levy, Michael A.
Kerkhof, Jennifer
Aref-Eshghi, Erfan
Schenkel, Laila
Stuart, Alan
McConkey, Haley
Henneman, Peter
Venema, Andrea
Schwartz, Charles E.
Stevenson, Roger E.
Skinner, Steven A.
DuPont, Barbara R.
Fletcher, Robin S.
Balci, Tugce B.
Siu, Victoria Mok
Granadillo, Jorge L.
Masters, Jennefer
Kadour, Mike
Friez, Michael J.
van Haelst, Mieke M.
Mannens, Marcel M. A. M.
Louie, Raymond J.
Lee, Jennifer A.
Tedder, Matthew L.
Alders, Marielle

January 2021

The original version of this article unfortunately contained a mistake. The following correction has...

Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

Francesco Vetrini
Shane McKee
Jill A. Rosenfeld
Mohnish Suri
Andrea M. Lewis
Kimberly Margaret Nugent
Elizabeth Roeder
Rebecca O. Littlejohn
Sue Holder
Wenmiao Zhu
Joseph T. Alaimo
Brett Graham
Jill M. Harris
James B. Gibson
Matthew Pastore
Kim L. McBride
Makanko Komara
Lihadh Al-Gazali
Aisha Al Shamsi
Elizabeth A. Fanning
Klaas J. Wierenga
Daryl A. Scott
Ziva Ben-Neriah
Vardiella Meiner
Hanoch Cassuto
Orly Elpeleg
J. Lloyd Holder Jr
Lindsay C. Burrage
Laurie H. Seaver
Lionel Van Maldergem
Sonal Mahida
Janet S. Soul
Margaret Marlatt
Ludmila Matyakhina
Julie Vogt
June-Anne Gold
Soo-Mi Park
Vinod Varghese
Anne K. Lampe
Ajith Kumar
Melissa Lees
Muriel Holder-Espinasse
Vivienne McConnell
Birgitta Bernhard
Ed Blair
Victoria Harrison
The DDD study
Donna M. Muzny
Richard A. Gibbs
Sarah H. Elsea
Jennifer E. Posey
Weimin Bi
Seema Lalani
Fan Xia
Yaping Yang
Christine M. Eng
James R. Lupski
Pengfei Liu

March 2019

It was highlighted that the original article [1] contained a typographical error in the Results sect...

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

Sanders, Stephan J
Neale, Benjamin M
Huang, Hailiang
Werling, Donna M
An, Joon-Yong
Dong, Shan
Abecasis, Goncalo
Arguello, P Alexander
Blangero, John
Boehnke, Michael
Daly, Mark J
Eggan, Kevin
Geschwind, Daniel H
Glahn, David C
Goldstein, David B
Gur, Raquel E
Handsaker, Robert E
McCarroll, Steven A
Ophoff, Roel A
Palotie, Aarno
Pato, Carlos N
Sabatti, Chiara
State, Matthew W
Willsey, A Jeremy
Hyman, Steven E
Addington, Anjene M
Lehner, Thomas
Freimer, Nelson B
Whole Genome Sequencing for Psychiatric Disorders (WGSPD)

July 2018

In the version of this article initially published, the consortium authorship and corresponding auth...

Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

Ferdinandusse, Sacha
McWalter, Kirsty
te Brinke, Heleen
IJlst, Lodewijk
Mooijer, Petra M.
Ruiter, Jos P.N.
van Lint, Alida E.M.
Pras-Raves, Mia
Wever, Eric
Millan, Francisca
Guillen Sacoto, Maria J.
Begtrup, Amber
Tarnopolsky, Mark
Brady, Lauren
Ladda, Roger L.
Sell, Susan L.
Nowak, Catherine B.
Douglas, Jessica
Tian, Cuixia
Ulm, Elizabeth
Perlman, Seth
Drack, Arlene V.
Chong, Karen
Martin, Nicole
Brault, Jennifer
Brokamp, Elly
Toro, Camilo
Gahl, William A.
Macnamara, Ellen F.
Wolfe, Lynne A.
Alejandro, Mercedes E.
Azamian, Mahshid S.
Bacino, Carlos A.
Balasubramanyam, Ashok
Burrage, Lindsay C.
Chao, Hsiao Tuan
Clark, Gary D.
Craigen, William J.
Dai, Hongzheng
Dhar, Shweta U.
Emrick, Lisa T.
Goldman, Alica M.
Hanchard, Neil A.
Jamal, Fariha
Karaviti, Lefkothea
Lalani, Seema R.
Lee, Brendan H.
Lewis, Richard A.
Marom, Ronit
Moretti, Paolo
Murdock, David R.
Nicholas, Sarah K.
Orengo, James P.
Posey, Jennifer E.
Potocki, Lorraine
Rosenfeld, Jill A.
Samson, Susan L.
Scott, Daryl A.
Tran, Alyssa A.
Vogel, Tiphanie P.
Wangler, Michael F.
Yamamoto, Shinya
Eng, Christine M.
Liu, Pengfei
Ward, Patricia A.
Behrens, Edward
Deardorff, Matthew
Falk, Marni
Hassey, Kelly
Sullivan, Kathleen
Vanderver, Adeline
Goldstein, David B.
Cope, Heidi
McConkie-Rosell, Allyn
Schoch, Kelly
Shashi, Vandana
Smith, Edward C.
Spillmann, Rebecca C.
Sullivan, Jennifer A.
Tan, Queenie K.G.
Walley, Nicole M.
Agrawal, Pankaj B.
Beggs, Alan H.
Berry, Gerard T.
Briere, Lauren C.
Cobban, Laurel A.
Coggins, Matthew
Cooper, Cynthia M.
Fieg, Elizabeth L.
High, Frances
Holm, Ingrid A.
Korrick, Susan
Krier, Joel B.
Lincoln, Sharyn A.
Loscalzo, Joseph
Maas, Richard L.
MacRae, Calum A.
Pallais, J. Carl
Rao, Deepak A.
Rodan, Lance H.
Silverman, Edwin K.
Stoler, Joan M.
Sweetser, David A.
Walker, Melissa
Walsh, Chris A.
Esteves, Cecilia
Kelley, Emily G.
Kohane, Isaac S.
LeBlanc, Kimberly
McCray, Alexa T.
Nagy, Anna
Dasari, Surendra
Lanpher, Brendan C.
Lanza, Ian R.
Morava, Eva
Oglesbee, Devin
Bademci, Guney
Barbouth, Deborah
Bivona, Stephanie
Carrasquillo, Olveen
Chang, Ta Chen Peter
Forghani, Irman
Grajewski, Alana
Isasi, Rosario
Lam, Byron
Levitt, Roy
Liu, Xue Zhong
McCauley, Jacob
Sacco, Ralph
Saporta, Mario
Schaechter, Judy
Tekin, Mustafa
Telischi, Fred
Thorson, Willa
Zuchner, Stephan
Colley, Heather A.
Dayal, Jyoti G.
Eckstein, David J.
Findley, Laurie C.
Krasnewich, Donna M.
Mamounas, Laura A.
Manolio, Teri A.
Mulvihill, John J.
LaMoure, Grace L.
Goldrich, Madison P.
Urv, Tiina K.
Doss, Argenia L.
Acosta, Maria T.
Bonnenmann, Carsten
D’Souza, Precilla
Draper, David D.
Ferreira, Carlos
Godfrey, Rena A.
Groden, Catherine A.
Macnamara, Ellen F.
Maduro, Valerie V.
Markello, Thomas C.
Nath, Avi
Novacic, Donna
Pusey, Barbara N.
Toro, Camilo
Wahl, Colleen E.
Baker, Eva
Burke, Elizabeth A.
Adams, David R.
Gahl, William A.
Malicdan, May Christine V.
Tifft, Cynthia J.
Wolfe, Lynne A.
Yang, John
Power, Bradley
Gochuico, Bernadette
Huryn, Laryssa
Latham, Lea
Davis, Joie
Mosbrook-Davis, Deborah
Rossignol, Francis
Solomon, Ben
MacDowall, John
Thurm, Audrey
Zein, Wadih
Yousef, Muhammad
Adam, Margaret
Amendola, Laura
Bamshad, Michael
Beck, Anita
Bennett, Jimmy
Berg-Rood, Beverly
Blue, Elizabeth
Boyd, Brenna
Byers, Peter
Chanprasert, Sirisak
Cunningham, Michael
Dipple, Katrina
Doherty, Daniel
Earl, Dawn
Glass, Ian
Golden-Grant, Katie
Hahn, Sihoun
Hing, Anne
Hisama, Fuki M.
Horike-Pyne, Martha
Jarvik, Gail P.
Jarvik, Jeffrey
Jayadev, Suman
Lam, Christina
Maravilla, Kenneth
Mefford, Heather
Merritt, J. Lawrence
Mirzaa, Ghayda
Nickerson, Deborah
Raskind, Wendy
Rosenwasser, Natalie
Scott, C. Ron
Sun, Angela
Sybert, Virginia
Wallace, Stephanie
Wener, Mark
Wenger, Tara
Ashley, Euan A.
Bejerano, Gill
Bernstein, Jonathan A.
Bonner, Devon
Coakley, Terra R.
Fernandez, Liliana
Fisher, Paul G.
Fresard, Laure
Hom, Jason
Huang, Yong
Kohler, Jennefer N.
Kravets, Elijah
Majcherska, Marta M.
Martin, Beth A.
Marwaha, Shruti
McCormack, Colleen E.
Raja, Archana N.
Reuter, Chloe M.
Ruzhnikov, Maura
Sampson, Jacinda B.
Smith, Kevin S.
Sutton, Shirley
Tabor, Holly K.
Tucker, Brianna M.
Wheeler, Matthew T.
Zastrow, Diane B.
Zhao, Chunli
Byrd, William E.
Crouse, Andrew B.
Might, Matthew
Nakano-Okuno, Mariko
Whitlock, Jordan
Brown, Gabrielle
Butte, Manish J.
Dell’Angelica, Esteban C.
Dorrani, Naghmeh
Douine, Emilie D.
Fogel, Brent L.
Gutierrez, Irma
Huang, Alden
Krakow, Deborah
Lee, Hane
Loo, Sandra K.
Mak, Bryan C.
Martin, Martin G.
Martínez-Agosto, Julian A.
McGee, Elisabeth
Nelson, Stanley F.
Nieves-Rodriguez, Shirley
Palmer, Christina G.S.
Papp, Jeanette C.
Parker, Neil H.
Renteria, Genecee
Signer, Rebecca H.
Sinsheimer, Janet S.
Wan, Jijun
Wang, Lee kai
Perry, Katherine Wesseling
Woods, Jeremy D.
Alvey, Justin
Andrews, Ashley
Bale, Jim
Bohnsack, John
Botto, Lorenzo
Carey, John
Pace, Laura
Longo, Nicola
Marth, Gabor
Moretti, Paolo
Quinlan, Aaron
Velinder, Matt
Viskochil, Dave
Bayrak-Toydemir, Pinar
Mao, Rong
Westerfield, Monte
Bican, Anna
Brokamp, Elly
Duncan, Laura
Hamid, Rizwan
Kennedy, Jennifer
Kozuira, Mary
Newman, John H.
Phillips, John A.
Rives, Lynette
Robertson, Amy K.
Solem, Emily
Cogan, Joy D.
Cole, F. Sessions
Hayes, Nichole
Kiley, Dana
Sisco, Kathy
Wambach, Jennifer
Wegner, Daniel
Baldridge, Dustin
Pak, Stephen
Schedl, Timothy
Shin, Jimann
Solnica-Krezel, Lilianna
Waisfisz, Quinten
Zwijnenburg, Petra J.G.
Ziegler, Alban
Barth, Magalie
Smith, Rosemarie
Ellingwood, Sara
Gaebler-Spira, Deborah
Bakhtiari, Somayeh
Kruer, Michael C.
van Kampen, Antoine H.C.
Wanders, Ronald J.A.
Waterham, Hans R.
Cassiman, David
Vaz, Frédéric M.

January 2021

In the original author list, Seth Perlman’s degrees were listed as MD, PhD. Dr Perlman’s degree is M...

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia (Nature Genetics, (2019), 51, 4, (649-658), 10.1038/s41588-019-0372-4)

Cortese A.
Simone R.
Sullivan R.
Vandrovcova J.
Tariq H.
Yau W. Y.
Humphrey J.
Jaunmuktane Z.
Sivakumar P.
Polke J.
Ilyas M.
Tribollet E.
Tomaselli P. J.
Devigili G.
Callegari I.
Versino M.
Salpietro V.
Efthymiou S.
Kaski D.
Wood N. W.
Andrade N. S.
Buglo E.
Rebelo A.
Rossor A. M.
Bronstein A.
Fratta P.
Marques W. J.
Zuchner S.
Reilly M. M.
Houlden H.

January 2019

In the version of this article initially published, the name of author Wai Yan Yau was misspelled. T...

Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Jaber Lyahyai
Bouchra Ouled Amar Bencheikh
Siham C. Elalaoui
Maria Mansouri
Lamia Boualla
Alexandre DIonne-Laporte
Dan Spiegelman
Patrick A. Dion
Patrick Cossette
Guy A. Rouleau
Abdelaziz Sefiani

April 2018

After publication of the original article [1] it was brought to our attention that author Bouchra Ou...

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

van Rheenen, W.
van der Spek, R.A.A.
Bakker, M.K.
van Vugt, J.J.F.A.
Hop, P.J.
Zwamborn, R.A.J.
de Klein, N.
Westra, H-J
Bakker, O.B.
Deelen, P.
Shireby, G.
Hannon, E.
Moisse, M.
Baird, D.
Restuadi, R.
Dolzhenko, E.
Dekker, A.M.
Gawor, K.
Westeneng, H-J
Tazelaar, G.H.P.
van Eijk, K.R.
Kooyman, M.
Byrne, R.P.
Doherty, M.
Heverin, M.
Al Khleifat, A.
Iacoangeli, A.
Shatunov, A.
Ticozzi, N.
Cooper-Knock, J.
Smith, B.N.
Gromicho, M.
Chandran, S.
Pal, S.
Morrison, K.E.
Shaw, P.J.
Hardy, J.
Orrell, R.W.
Sendtner, M.
Meyer, T.
Başak, N.
van der Kooi, A.J.
Ratti, A.
Fogh, I.
Gellera, C.
Lauria, G.
Corti, S.
Cereda, C.
Sproviero, D.
D’alfonso, S.
Sorarù, G.
Siciliano, G.
Filosto, M.
Padovani, A.
Chiò, A.
Calvo, A.
Moglia, C.
Brunetti, M.
Canosa, A.
Grassano, M.
Beghi, E.
Pupillo, E.
Logroscino, G.
Nefussy, B.
Osmanovic, A.
Nordin, A.
Lerner, Y.
Zabari, M.
Gotkine, M.
Baloh, R.H.
Bell, S.
Vourc’h, P.
Corcia, P.
Couratier, P.
Millecamps, S.
Meininger, V.
Salachas, F.
Mora Pardina, J.S.
Assialioui, A.
Rojas-García, R.
Dion, P.A.
Ross, J.P.
Ludolph, A.C.
Weishaupt, J.H.
Brenner, D.
Freischmidt, A.
Bensimon, G.
Brice, A.
Durr, A.
Payan, C.A.M.
Saker-Delye, S.
Wood, N.W.
Topp, S.
Rademakers, R.
Tittmann, L.
Lieb, W.
Franke, A.
Ripke, S.
Braun, A.
Kraft, J.
Whiteman, D.C.
Olsen, C.M.
Uitterlinden, A.G.
Hofman, A.
Rietschel, M.
Cichon, S.
Nöthen, M.M.
Amouyel, P.
Comi, G.
Riva, N.
Lunetta, C.
Gerardi, F.
Cotelli, M.S.
Rinaldi, F.
Chiveri, L.
Guaita, M.C.
Perrone, P.
Ceroni, M.
Diamanti, L.
Ferrarese, C.
Tremolizzo, L.
Delodovici, M.L.
Bono, G.
Canosa, A.
Manera, U.
Vasta, R.
Bombaci, A.
Casale, F.
Fuda, G.
Salamone, P.
Iazzolino, B.
Peotta, L.
Cugnasco, P.
De Marco, G.
Torrieri, M.C.
Palumbo, F.
Gallone, S.
Barberis, M.
Sbaiz, L.
Gentile, S.
Mauro, A.
Mazzini, L.
De Marchi, F.
Corrado, L.
D’Alfonso, S.
Bertolotto, A.
Gionco, M.
Leotta, D.
Odddenino, E.
Imperiale, D.
Cavallo, R.
Pignatta, P.
De Mattei, M.
Geda, C.
Papurello, D.M.
Gusmaroli, G.
Comi, C.
Labate, C.
Ruiz, L.
Ferrandi, D.
Rota, E.
Aguggia, M.
Di Vito, N.
Meineri, P.
Ghiglione, P.
Launaro, N.
Dotta, M.
Di Sapio, A.
Giardini, G.
Tiloca, C.
Peverelli, S.
Taroni, F.
Pensato, V.
Castellotti, B.
Comi, G.P.
Del Bo, R.
Ceroni, M.
Gagliardi, S.
Corrado, L.
Mazzini, L.
Raggi, F.
Simoncini, C.
Lo Gerfo, A.
Inghilleri, M.
Ferlini, A.
Simone, I.L.
Passarella, B.
Guerra, V.
Zoccolella, S.
Nozzoli, C.
Mundi, C.
Leone, M.
Zarrelli, M.
Tamma, F.
Valluzzi, F.
Calabrese, G.
Boero, G.
Rini, A.
Traynor, B.J.
Singleton, A.B.
Mitne Neto, M.
Cauchi, R.J.
Ophoff, R.A.
Wiedau-Pazos, M.
Lomen-Hoerth, C.
van Deerlin, V.M.
Grosskreutz, J.
Roediger, A.
Gaur, N.
Jörk, A.
Barthel, T.
Theele, E.
Ilse, B.
Stubendorff, B.
Witte, O.W.
Steinbach, R.
Hübner, C.A.
Graff, C.
Brylev, L.
Fominykh, V.
Demeshonok, V.
Ataulina, A.
Rogelj, B.
Koritnik, B.
Zidar, J.
Ravnik-Glavač, M.
Glavač, D.
Stević, Z.
Drory, V.
Povedano, M.
Blair, I.P.
Kiernan, M.C.
Benyamin, B.
Henderson, R.D.
Furlong, S.
Mathers, S.
McCombe, P.A.
Needham, M.
Ngo, S.T.
Nicholson, G.A.
Pamphlett, R.
Rowe, D.B.
Steyn, F.J.
Williams, K.L.
Mather, K.A.
Sachdev, P.S.
Henders, A.K.
Wallace, L.
de Carvalho, M.
Pinto, S.
Petri, S.
Weber, M.
Rouleau, G.A.
Silani, V.
Curtis, C.J.
Breen, G.
Glass, J.D.
Brown, R.H.
Landers, J.E.
Shaw, C.E.
Andersen, P.M.
Groen, E.J.N.
van Es, M.A.
Pasterkamp, R.J.
Fan, D.
Garton, F.C.
McRae, A.F.
Davey Smith, G.
Gaunt, T.R.
Eberle, M.A.
Mill, J.
McLaughlin, R.L.
Hardiman, O.
Kenna, K.P.
Wray, N.R.
Tsai, E.
Runz, H.
Franke, L.
Al-Chalabi, A.
Van Damme, P.
van den Berg, L.H.
Veldink, J.H.

January 2022

Correction to: Nature Genetics https://doi.org/10.1038/s41588-021-00973-1, published online 6 Decemb...

de Boer E.
Ockeloen C. W.
Matalonga L.
Horvath R.
Cohen E.
Cuesta I.
Danis D.
Denomme-Pichon A. -S.
Duffourd Y.
Gilissen C.
Johari M.
Laurie S.
Li S.
Matalonga L.
Nelson I.
Peters S.
Paramonov I.
Prasanth S.
Robinson P.
Sablauskas K.
Savarese M.
Steyaert W.
Topf A.
van der Velde J. K.
Vitobello A.
Rodenburg R. J.
Coenen M. J. H.
Janssen M.
Henssen D.
Gilissen C.
Steyaert W.
Paramonov I.
Banka S.
Benetti E.
Casari G.
Ciolfi A.
Clayton-Smith J.
Dallapiccola B.
de Boer E.
Faivre L.
Haack T. B.
Hammarsjo A.
Havlovicova M.
Hoischen A.
Hugon A.
Jackson A.
Kleefstra T.
Lindstrand A.
Lopez-Martin E.
Macek M.
Nigro V.
Nordgren A.
Pettersson M.
Pinelli M.
Pizzi S.
Posada M.
Radio F. C.
Renieri A.
Rooryck C.
Ryba L.
Schwarz M.
Tartaglia M.
Thauvin C.
Torella A.
Verloes A.
Vissers L.
Vyshka K.
Zurek B.
Trimouille A.
Kleefstra T.
Verloes A.
Vissers L. E. L. M.

January 2021

In the original publication of the article, consortium author lists were missing in the article. The...

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Schüle, Rebecca
Timmann, Dagmar
Erasmus, Corrie E.
Reichbauer, Jennifer
Wayand, Melanie
van de Warrenburg, Bart
Schöls, Ludger
Wilke, Carlo
Bevot, Andrea
Zuchner, Stephan
Beltran, Sergi
Laurie, Steven
Matalonga, Leslie
Graessner, Holm
Synofzik, Matthis

September 2021

In the original publication of the article, consortium author lists were missing in the article

Bernard, Elsa
Nannya, Yasuhito
Hasserjian, Robert P.
Devlin, Sean M.
Tuechler, Heinz
Medina-Martinez, Juan S.
Yoshizato, Tetsuichi
Shiozawa, Yusuke
Saiki, Ryunosuke
Malcovati, Luca
Levine, Max F.
Arango, Juan E.
Zhou, Yangyu
Solé, Francesc
Cargo, Catherine A.
Haase, Detlef
Creignou, Maria
Germing, Ulrich
Zhang, Yanming
Gundem, Gunes
Sarian, Araxe
van de Loosdrecht, Arjan A.
Jädersten, Martin
Tobiasson, Magnus
Kosmider, Olivier
Follo, Matilde Y.
Thol, Felicitas
Pinheiro, Ronald F.
Santini, Valeria
Kotsianidis, Ioannis
Boultwood, Jacqueline
Santos, Fabio P. S.
Schanz, Julie
Kasahara, Senji
Ishikawa, Takayuki
Tsurumi, Hisashi
Takaori-Kondo, Akifumi
Kiguchi, Toru
Polprasert, Chantana
Bennett, John M.
Klimek, Virginia M.
Savona, Michael R.
Belickova, Monika
Ganster, Christina
Palomo, Laura
Sanz, Guillermo
Ades, Lionel
Della Porta, Matteo Giovanni
Elias, Harold K.
Smith, Alexandra G.
Werner, Yesenia
Patel, Minal
Viale, Agnès
Vanness, Katelynd
Neuberg, Donna S.
Stevenson, Kristen E.
Menghrajani, Kamal
Bolton, Kelly L.
Fenaux, Pierre
Pellagatti, Andrea
Platzbecker, Uwe
Heuser, Michael
Valent, Peter
Chiba, Shigeru
Miyazaki, Yasushi
Finelli, Carlo
Voso, Maria Teresa
Shih, Lee-Yung
Fontenay, Michaela
Jansen, Joop H.
Cervera, José
Atsuta, Yoshiko
Gattermann, Norbert
Ebert, Benjamin L.
Bejar, Rafael
Greenberg, Peter L.
Cazzola, Mario
Hellström-Lindberg, Eva
Ogawa, Seishi
Papaemmanuil, Elli

May 2021

In the version of this article initially published, one name (Harold K. Elias) was omitted from the ...

Taskesen, E
Mishra, A
van der Sluis, S
Ferrari, R
Veldink, J H
van Es, M A
Smit, A B
Posthuma, D
Pijnenburg, Y
Hernandez, DG
Nalls. MA
Rohrer JD
Ramasamy, A
Kwok, JBJ
Dobson-Stone, C
Schofield, PR
Halliday, GM
Hodges, JR
Piguet, O
Bartley, L
Thompson, E
Haan, E
Hernández, I
Ruiz, A
Boada, M
Borroni, B
Padovani, A
Cruchaga, C
Cairns, NJ
Benussi, L
Binetti G
Ghidoni, R
Forloni, G
Albani, D
Galimberti, D
Fenoglio, C
Serp
Wassermann EM
Baborie A
Jaros E
Tierney MC
Pastor P
Razquin C
Ortega-Cubero S
Alonso E
Perneczky R
Diehl-Schmid J
Alexopoulos P
Kurz A
Rainero I
Rubino E
Pinessi L
Rogaeva E
George-Hyslop PS
Rossi G
Tagliavini F
Giaccone G
Rowe JB
Schlachetzki JCM
Uphill J
Collinge J
Mead S
Danek A
Van Deerlin VM
Grossman M
Trojanowski JQ
van der Zee J
Van Broeckhoven C
Cappa SF
Leber I
Hannequin D
Golfier V
Vercelletto M
Brice A
Nacmias B
Sorbi S
Bagnoli S
Piaceri I
Nielsen JE
Hjermind LE
Riemenschneider M
Mayhaus M
Ibach B
Gasparoni G
Pichler S
Gu W
Rossor MN
Fox NC
Warren JD
Spillantini MG
Morris HR
Rizzu P
Heutink P
Snowden JS
Rollinson S
Richardson A
Gerhard A
Bruni AC
Maletta R
Frangipane F
Cupidi C
Bernardi L
Anfossi M
Gallo M
Conidi ME
Smirne N
Rademakers R
Baker M
Dickson DW
Graff-Radford NR
Petersen RC
Knopman D
Josephs KA
Boeve BF
Parisi JE
Seeley WW
Miller BL
Karydas AM
Rosen H
van Swieten JC
Dopper EGP
Seelaar H
Scheltens P
Logroscino G
Capozzo R
Novelli V
Puca AA
Franceschi M
Postiglione A
Milan G
Sorrentino P
Kristiansen M
Chiang HH
Graff C
Pasquier F
Rollin A
Deramecourt V
Lebouvier T
Kapogiannis D
Ferrucci L
Pickering-Brown S
Singleton AB
Hardy J
Momeni P.

January 2018

International FTD-Genomics Consortium was omitted from the author list in the original version of th...

Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

Nizon, Mathilde
Laugel, Vincent
Flanigan, Kevin
Pastore, Matthew
Waldrop, Megan
Rosenfeld, Jill
Marom, Ronit
Xiao, Rui
Gerard, Amanda
Pichon, Olivier
Le Caignec, Cédric
Gérard, Marion
Dieterich, Klaus
Truitt Cho, Megan
Mcwalter, Kirsty
Hiatt, Susan
Thompson, Michelle
Bézieau, Stéphane
Wadley, Alexandrea
Wierenga, Klaas
Egly, Jean-Marc
Isidor, Bertrand

November 2019

International audienceIn the Acknowledgements section of the paper the authors neglected to mention ...

Bis, J.C. (Joshua)
Jian, X. (Xueqiu)
Kunkle, B.W. (Brian W.)
Chen, Y. (Yuning)
Hamilton-Nelson, K.L. (Kara L.)
Bush, W.S. (William S.)
Salerno, W.J. (William J.)
Lancour, D. (Daniel)
Ma, Y. (Yiyi)
Renton, A. (Alan)
Marcora, E. (Edoardo)
Farrell, J.J. (John J.)
Zhao, Y. (Yi)
Qu, L. (Liming)
Ahmad, S. (Shahzad)
Amin, N. (Najaf)
Amouyel, P. (Philippe)
Beecham, G.W.
Below, J.E. (Jennifer E.)
Campion, D. (Dominique)
Cantwell, L.B. (Laura B.)
Charbonnier, C. (Camille)
Chung, J. (Jaeyoon)
Crane, P.K. (Paul K.)
Crane, L.M.A.
Cupples, L.A. (L. Adrienne)
Dartigues, J.-F.
Debette, S. (Stéphanie)
Deleuze, J.-F. (Jean-François)
Fulton, L. (Lucinda)
Gabriel, S.B. (Stacey)
Genin, E. (Emmanuelle)
Gibbs, R.A. (Richard)
Goate, A. (Alison)
Grenier-Boley, B. (Benjamin)
Gupta, N. (Namrata)
Haines, J.L. (Jonathan)
Havulinna, A.S. (Aki)
Helisalmi, S. (Seppo)
Hiltunen, M. (Mikko)
Howrigan, D.P. (Daniel P.)
Ikram, M.A. (Arfan)
Kaprio, J. (Jaakko)
Konrad, J. (Jan)
Kuzma, A. (Amanda)
Lander, E.S. (Eric)
Lathrop, M. (Mark)
Lehtimäki, T. (Terho)
Lin, H. (Honghuang)
Mattila, K. (Kari)
Mayeux, R. (Richard)
Muzny, D. (Donna)
Nasser, W. (Waleed)
Neale, B.M. (Benjamin)
Nho, K. (Kwangsik)
Nicolas, G. (Gaël)
Patel, D. (Devanshi)
Kunkle, B. (Brian)
Perola, M. (Markus)
Psaty, B.M. (Bruce)
Quenez, O. (Olivier)
Rajabli, F. (Farid)
Redon, R. (Richard)
Reitz, C. (Christiane)
Remes, A. (Anne)
Salomaa, V. (Veikko)
Sarnowski, C.
Schmidt, H. (Helena)
Schmidt, M. (Michael)
Schmidt, R. (Reinhold)
Soininen, H. (H.)
Thornton, T.A. (Timothy A.)
Tosto, G. (G.)
Tzourio, C. (Christophe)
Lee, S.J. (Sven) van der
Duijn, C.M. (Cornelia) van
Valladares, O. (Otto)
Vardarajan, B.N. (Badri)
Wang, L.S. (Li-San)
Wang, W. (Weixin)
Wijsman, E. (Ellen)
Wilson, R.K. (Richard K.)
Witten, D. (Daniela)
Worley, K.C. (Kim C.)
Zhang, X. (Xiaoling)
Bellenguez, C. (Céline)
Lambert, J.-C. (J.)
Kurki, M.I. (Mitja I.)
Palotie, A. (Aarno)
Daly, M.J. (Mark)
Boerwinkle, E.A. (Eric)
Lunetta, K.L. (Kathryn)
DeStefano, A.L. (Anita)
Amin, N. (Najaf)
Martin, E.R.
Schellenberg, G.D. (Gerard)
Seshadri, S. (Sudha)
Naj, A.C. (Adam C.)
Fornage, M. (Myriam)
Farrer, L.A. (Lindsay)

January 2019

Following publication, the authors noticed that ‘Laura Cantwell’, ‘Otto Valladares’, and ‘Li-San Wan...

Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders (Genetics in Medicine, (2021), 10.1038/s41436-020-01096-4)

Sadikovic, Bekim
Levy, Michael A.
Kerkhof, Jennifer
Aref-Eshghi, Erfan
Schenkel, Laila
Stuart, Alan
McConkey, Haley
Henneman, Peter
Venema, Andrea
Schwartz, Charles E.
Stevenson, Roger E.
Skinner, Steven A.
DuPont, Barbara R.
Fletcher, Robin S.
Balci, Tugce B.
Siu, Victoria Mok
Granadillo, Jorge L.
Masters, Jennefer
Kadour, Mike
Friez, Michael J.
van Haelst, Mieke M.
Mannens, Marcel M. A. M.
Louie, Raymond J.
Lee, Jennifer A.
Tedder, Matthew L.
Alders, Marielle

January 2021

The original version of this article unfortunately contained a mistake. The following correction has...

Francesco Vetrini
Shane McKee
Jill A. Rosenfeld
Mohnish Suri
Andrea M. Lewis
Kimberly Margaret Nugent
Elizabeth Roeder
Rebecca O. Littlejohn
Sue Holder
Wenmiao Zhu
Joseph T. Alaimo
Brett Graham
Jill M. Harris
James B. Gibson
Matthew Pastore
Kim L. McBride
Makanko Komara
Lihadh Al-Gazali
Aisha Al Shamsi
Elizabeth A. Fanning
Klaas J. Wierenga
Daryl A. Scott
Ziva Ben-Neriah
Vardiella Meiner
Hanoch Cassuto
Orly Elpeleg
J. Lloyd Holder Jr
Lindsay C. Burrage
Laurie H. Seaver
Lionel Van Maldergem
Sonal Mahida
Janet S. Soul
Margaret Marlatt
Ludmila Matyakhina
Julie Vogt
June-Anne Gold
Soo-Mi Park
Vinod Varghese
Anne K. Lampe
Ajith Kumar
Melissa Lees
Muriel Holder-Espinasse
Vivienne McConnell
Birgitta Bernhard
Ed Blair
Victoria Harrison
The DDD study
Donna M. Muzny
Richard A. Gibbs
Sarah H. Elsea
Jennifer E. Posey
Weimin Bi
Seema Lalani
Fan Xia
Yaping Yang
Christine M. Eng
James R. Lupski
Pengfei Liu

March 2019

It was highlighted that the original article [1] contained a typographical error in the Results sect...

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

Sanders, Stephan J
Neale, Benjamin M
Huang, Hailiang
Werling, Donna M
An, Joon-Yong
Dong, Shan
Abecasis, Goncalo
Arguello, P Alexander
Blangero, John
Boehnke, Michael
Daly, Mark J
Eggan, Kevin
Geschwind, Daniel H
Glahn, David C
Goldstein, David B
Gur, Raquel E
Handsaker, Robert E
McCarroll, Steven A
Ophoff, Roel A
Palotie, Aarno
Pato, Carlos N
Sabatti, Chiara
State, Matthew W
Willsey, A Jeremy
Hyman, Steven E
Addington, Anjene M
Lehner, Thomas
Freimer, Nelson B
Whole Genome Sequencing for Psychiatric Disorders (WGSPD)

July 2018

In the version of this article initially published, the consortium authorship and corresponding auth...

Ferdinandusse, Sacha
McWalter, Kirsty
te Brinke, Heleen
IJlst, Lodewijk
Mooijer, Petra M.
Ruiter, Jos P.N.
van Lint, Alida E.M.
Pras-Raves, Mia
Wever, Eric
Millan, Francisca
Guillen Sacoto, Maria J.
Begtrup, Amber
Tarnopolsky, Mark
Brady, Lauren
Ladda, Roger L.
Sell, Susan L.
Nowak, Catherine B.
Douglas, Jessica
Tian, Cuixia
Ulm, Elizabeth
Perlman, Seth
Drack, Arlene V.
Chong, Karen
Martin, Nicole
Brault, Jennifer
Brokamp, Elly
Toro, Camilo
Gahl, William A.
Macnamara, Ellen F.
Wolfe, Lynne A.
Alejandro, Mercedes E.
Azamian, Mahshid S.
Bacino, Carlos A.
Balasubramanyam, Ashok
Burrage, Lindsay C.
Chao, Hsiao Tuan
Clark, Gary D.
Craigen, William J.
Dai, Hongzheng
Dhar, Shweta U.
Emrick, Lisa T.
Goldman, Alica M.
Hanchard, Neil A.
Jamal, Fariha
Karaviti, Lefkothea
Lalani, Seema R.
Lee, Brendan H.
Lewis, Richard A.
Marom, Ronit
Moretti, Paolo
Murdock, David R.
Nicholas, Sarah K.
Orengo, James P.
Posey, Jennifer E.
Potocki, Lorraine
Rosenfeld, Jill A.
Samson, Susan L.
Scott, Daryl A.
Tran, Alyssa A.
Vogel, Tiphanie P.
Wangler, Michael F.
Yamamoto, Shinya
Eng, Christine M.
Liu, Pengfei
Ward, Patricia A.
Behrens, Edward
Deardorff, Matthew
Falk, Marni
Hassey, Kelly
Sullivan, Kathleen
Vanderver, Adeline
Goldstein, David B.
Cope, Heidi
McConkie-Rosell, Allyn
Schoch, Kelly
Shashi, Vandana
Smith, Edward C.
Spillmann, Rebecca C.
Sullivan, Jennifer A.
Tan, Queenie K.G.
Walley, Nicole M.
Agrawal, Pankaj B.
Beggs, Alan H.
Berry, Gerard T.
Briere, Lauren C.
Cobban, Laurel A.
Coggins, Matthew
Cooper, Cynthia M.
Fieg, Elizabeth L.
High, Frances
Holm, Ingrid A.
Korrick, Susan
Krier, Joel B.
Lincoln, Sharyn A.
Loscalzo, Joseph
Maas, Richard L.
MacRae, Calum A.
Pallais, J. Carl
Rao, Deepak A.
Rodan, Lance H.
Silverman, Edwin K.
Stoler, Joan M.
Sweetser, David A.
Walker, Melissa
Walsh, Chris A.
Esteves, Cecilia
Kelley, Emily G.
Kohane, Isaac S.
LeBlanc, Kimberly
McCray, Alexa T.
Nagy, Anna
Dasari, Surendra
Lanpher, Brendan C.
Lanza, Ian R.
Morava, Eva
Oglesbee, Devin
Bademci, Guney
Barbouth, Deborah
Bivona, Stephanie
Carrasquillo, Olveen
Chang, Ta Chen Peter
Forghani, Irman
Grajewski, Alana
Isasi, Rosario
Lam, Byron
Levitt, Roy
Liu, Xue Zhong
McCauley, Jacob
Sacco, Ralph
Saporta, Mario
Schaechter, Judy
Tekin, Mustafa
Telischi, Fred
Thorson, Willa
Zuchner, Stephan
Colley, Heather A.
Dayal, Jyoti G.
Eckstein, David J.
Findley, Laurie C.
Krasnewich, Donna M.
Mamounas, Laura A.
Manolio, Teri A.
Mulvihill, John J.
LaMoure, Grace L.
Goldrich, Madison P.
Urv, Tiina K.
Doss, Argenia L.
Acosta, Maria T.
Bonnenmann, Carsten
D’Souza, Precilla
Draper, David D.
Ferreira, Carlos
Godfrey, Rena A.
Groden, Catherine A.
Macnamara, Ellen F.
Maduro, Valerie V.
Markello, Thomas C.
Nath, Avi
Novacic, Donna
Pusey, Barbara N.
Toro, Camilo
Wahl, Colleen E.
Baker, Eva
Burke, Elizabeth A.
Adams, David R.
Gahl, William A.
Malicdan, May Christine V.
Tifft, Cynthia J.
Wolfe, Lynne A.
Yang, John
Power, Bradley
Gochuico, Bernadette
Huryn, Laryssa
Latham, Lea
Davis, Joie
Mosbrook-Davis, Deborah
Rossignol, Francis
Solomon, Ben
MacDowall, John
Thurm, Audrey
Zein, Wadih
Yousef, Muhammad
Adam, Margaret
Amendola, Laura
Bamshad, Michael
Beck, Anita
Bennett, Jimmy
Berg-Rood, Beverly
Blue, Elizabeth
Boyd, Brenna
Byers, Peter
Chanprasert, Sirisak
Cunningham, Michael
Dipple, Katrina
Doherty, Daniel
Earl, Dawn
Glass, Ian
Golden-Grant, Katie
Hahn, Sihoun
Hing, Anne
Hisama, Fuki M.
Horike-Pyne, Martha
Jarvik, Gail P.
Jarvik, Jeffrey
Jayadev, Suman
Lam, Christina
Maravilla, Kenneth
Mefford, Heather
Merritt, J. Lawrence
Mirzaa, Ghayda
Nickerson, Deborah
Raskind, Wendy
Rosenwasser, Natalie
Scott, C. Ron
Sun, Angela
Sybert, Virginia
Wallace, Stephanie
Wener, Mark
Wenger, Tara
Ashley, Euan A.
Bejerano, Gill
Bernstein, Jonathan A.
Bonner, Devon
Coakley, Terra R.
Fernandez, Liliana
Fisher, Paul G.
Fresard, Laure
Hom, Jason
Huang, Yong
Kohler, Jennefer N.
Kravets, Elijah
Majcherska, Marta M.
Martin, Beth A.
Marwaha, Shruti
McCormack, Colleen E.
Raja, Archana N.
Reuter, Chloe M.
Ruzhnikov, Maura
Sampson, Jacinda B.
Smith, Kevin S.
Sutton, Shirley
Tabor, Holly K.
Tucker, Brianna M.
Wheeler, Matthew T.
Zastrow, Diane B.
Zhao, Chunli
Byrd, William E.
Crouse, Andrew B.
Might, Matthew
Nakano-Okuno, Mariko
Whitlock, Jordan
Brown, Gabrielle
Butte, Manish J.
Dell’Angelica, Esteban C.
Dorrani, Naghmeh
Douine, Emilie D.
Fogel, Brent L.
Gutierrez, Irma
Huang, Alden
Krakow, Deborah
Lee, Hane
Loo, Sandra K.
Mak, Bryan C.
Martin, Martin G.
Martínez-Agosto, Julian A.
McGee, Elisabeth
Nelson, Stanley F.
Nieves-Rodriguez, Shirley
Palmer, Christina G.S.
Papp, Jeanette C.
Parker, Neil H.
Renteria, Genecee
Signer, Rebecca H.
Sinsheimer, Janet S.
Wan, Jijun
Wang, Lee kai
Perry, Katherine Wesseling
Woods, Jeremy D.
Alvey, Justin
Andrews, Ashley
Bale, Jim
Bohnsack, John
Botto, Lorenzo
Carey, John
Pace, Laura
Longo, Nicola
Marth, Gabor
Moretti, Paolo
Quinlan, Aaron
Velinder, Matt
Viskochil, Dave
Bayrak-Toydemir, Pinar
Mao, Rong
Westerfield, Monte
Bican, Anna
Brokamp, Elly
Duncan, Laura
Hamid, Rizwan
Kennedy, Jennifer
Kozuira, Mary
Newman, John H.
Phillips, John A.
Rives, Lynette
Robertson, Amy K.
Solem, Emily
Cogan, Joy D.
Cole, F. Sessions
Hayes, Nichole
Kiley, Dana
Sisco, Kathy
Wambach, Jennifer
Wegner, Daniel
Baldridge, Dustin
Pak, Stephen
Schedl, Timothy
Shin, Jimann
Solnica-Krezel, Lilianna
Waisfisz, Quinten
Zwijnenburg, Petra J.G.
Ziegler, Alban
Barth, Magalie
Smith, Rosemarie
Ellingwood, Sara
Gaebler-Spira, Deborah
Bakhtiari, Somayeh
Kruer, Michael C.
van Kampen, Antoine H.C.
Wanders, Ronald J.A.
Waterham, Hans R.
Cassiman, David
Vaz, Frédéric M.

January 2021

In the original author list, Seth Perlman’s degrees were listed as MD, PhD. Dr Perlman’s degree is M...

Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia (Nature Genetics, (2019), 51, 4, (649-658), 10.1038/s41588-019-0372-4)

Cortese A.
Simone R.
Sullivan R.
Vandrovcova J.
Tariq H.
Yau W. Y.
Humphrey J.
Jaunmuktane Z.
Sivakumar P.
Polke J.
Ilyas M.
Tribollet E.
Tomaselli P. J.
Devigili G.
Callegari I.
Versino M.
Salpietro V.
Efthymiou S.
Kaski D.
Wood N. W.
Andrade N. S.
Buglo E.
Rebelo A.
Rossor A. M.
Bronstein A.
Fratta P.
Marques W. J.
Zuchner S.
Reilly M. M.
Houlden H.

January 2019

In the version of this article initially published, the name of author Wai Yan Yau was misspelled. T...

Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

Jaber Lyahyai
Bouchra Ouled Amar Bencheikh
Siham C. Elalaoui
Maria Mansouri
Lamia Boualla
Alexandre DIonne-Laporte
Dan Spiegelman
Patrick A. Dion
Patrick Cossette
Guy A. Rouleau
Abdelaziz Sefiani

April 2018

After publication of the original article [1] it was brought to our attention that author Bouchra Ou...

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

van Rheenen, W.
van der Spek, R.A.A.
Bakker, M.K.
van Vugt, J.J.F.A.
Hop, P.J.
Zwamborn, R.A.J.
de Klein, N.
Westra, H-J
Bakker, O.B.
Deelen, P.
Shireby, G.
Hannon, E.
Moisse, M.
Baird, D.
Restuadi, R.
Dolzhenko, E.
Dekker, A.M.
Gawor, K.
Westeneng, H-J
Tazelaar, G.H.P.
van Eijk, K.R.
Kooyman, M.
Byrne, R.P.
Doherty, M.
Heverin, M.
Al Khleifat, A.
Iacoangeli, A.
Shatunov, A.
Ticozzi, N.
Cooper-Knock, J.
Smith, B.N.
Gromicho, M.
Chandran, S.
Pal, S.
Morrison, K.E.
Shaw, P.J.
Hardy, J.
Orrell, R.W.
Sendtner, M.
Meyer, T.
Başak, N.
van der Kooi, A.J.
Ratti, A.
Fogh, I.
Gellera, C.
Lauria, G.
Corti, S.
Cereda, C.
Sproviero, D.
D’alfonso, S.
Sorarù, G.
Siciliano, G.
Filosto, M.
Padovani, A.
Chiò, A.
Calvo, A.
Moglia, C.
Brunetti, M.
Canosa, A.
Grassano, M.
Beghi, E.
Pupillo, E.
Logroscino, G.
Nefussy, B.
Osmanovic, A.
Nordin, A.
Lerner, Y.
Zabari, M.
Gotkine, M.
Baloh, R.H.
Bell, S.
Vourc’h, P.
Corcia, P.
Couratier, P.
Millecamps, S.
Meininger, V.
Salachas, F.
Mora Pardina, J.S.
Assialioui, A.
Rojas-García, R.
Dion, P.A.
Ross, J.P.
Ludolph, A.C.
Weishaupt, J.H.
Brenner, D.
Freischmidt, A.
Bensimon, G.
Brice, A.
Durr, A.
Payan, C.A.M.
Saker-Delye, S.
Wood, N.W.
Topp, S.
Rademakers, R.
Tittmann, L.
Lieb, W.
Franke, A.
Ripke, S.
Braun, A.
Kraft, J.
Whiteman, D.C.
Olsen, C.M.
Uitterlinden, A.G.
Hofman, A.
Rietschel, M.
Cichon, S.
Nöthen, M.M.
Amouyel, P.
Comi, G.
Riva, N.
Lunetta, C.
Gerardi, F.
Cotelli, M.S.
Rinaldi, F.
Chiveri, L.
Guaita, M.C.
Perrone, P.
Ceroni, M.
Diamanti, L.
Ferrarese, C.
Tremolizzo, L.
Delodovici, M.L.
Bono, G.
Canosa, A.
Manera, U.
Vasta, R.
Bombaci, A.
Casale, F.
Fuda, G.
Salamone, P.
Iazzolino, B.
Peotta, L.
Cugnasco, P.
De Marco, G.
Torrieri, M.C.
Palumbo, F.
Gallone, S.
Barberis, M.
Sbaiz, L.
Gentile, S.
Mauro, A.
Mazzini, L.
De Marchi, F.
Corrado, L.
D’Alfonso, S.
Bertolotto, A.
Gionco, M.
Leotta, D.
Odddenino, E.
Imperiale, D.
Cavallo, R.
Pignatta, P.
De Mattei, M.
Geda, C.
Papurello, D.M.
Gusmaroli, G.
Comi, C.
Labate, C.
Ruiz, L.
Ferrandi, D.
Rota, E.
Aguggia, M.
Di Vito, N.
Meineri, P.
Ghiglione, P.
Launaro, N.
Dotta, M.
Di Sapio, A.
Giardini, G.
Tiloca, C.
Peverelli, S.
Taroni, F.
Pensato, V.
Castellotti, B.
Comi, G.P.
Del Bo, R.
Ceroni, M.
Gagliardi, S.
Corrado, L.
Mazzini, L.
Raggi, F.
Simoncini, C.
Lo Gerfo, A.
Inghilleri, M.
Ferlini, A.
Simone, I.L.
Passarella, B.
Guerra, V.
Zoccolella, S.
Nozzoli, C.
Mundi, C.
Leone, M.
Zarrelli, M.
Tamma, F.
Valluzzi, F.
Calabrese, G.
Boero, G.
Rini, A.
Traynor, B.J.
Singleton, A.B.
Mitne Neto, M.
Cauchi, R.J.
Ophoff, R.A.
Wiedau-Pazos, M.
Lomen-Hoerth, C.
van Deerlin, V.M.
Grosskreutz, J.
Roediger, A.
Gaur, N.
Jörk, A.
Barthel, T.
Theele, E.
Ilse, B.
Stubendorff, B.
Witte, O.W.
Steinbach, R.
Hübner, C.A.
Graff, C.
Brylev, L.
Fominykh, V.
Demeshonok, V.
Ataulina, A.
Rogelj, B.
Koritnik, B.
Zidar, J.
Ravnik-Glavač, M.
Glavač, D.
Stević, Z.
Drory, V.
Povedano, M.
Blair, I.P.
Kiernan, M.C.
Benyamin, B.
Henderson, R.D.
Furlong, S.
Mathers, S.
McCombe, P.A.
Needham, M.
Ngo, S.T.
Nicholson, G.A.
Pamphlett, R.
Rowe, D.B.
Steyn, F.J.
Williams, K.L.
Mather, K.A.
Sachdev, P.S.
Henders, A.K.
Wallace, L.
de Carvalho, M.
Pinto, S.
Petri, S.
Weber, M.
Rouleau, G.A.
Silani, V.
Curtis, C.J.
Breen, G.
Glass, J.D.
Brown, R.H.
Landers, J.E.
Shaw, C.E.
Andersen, P.M.
Groen, E.J.N.
van Es, M.A.
Pasterkamp, R.J.
Fan, D.
Garton, F.C.
McRae, A.F.
Davey Smith, G.
Gaunt, T.R.
Eberle, M.A.
Mill, J.
McLaughlin, R.L.
Hardiman, O.
Kenna, K.P.
Wray, N.R.
Tsai, E.
Runz, H.
Franke, L.
Al-Chalabi, A.
Van Damme, P.
van den Berg, L.H.
Veldink, J.H.

January 2022

Correction to: Nature Genetics https://doi.org/10.1038/s41588-021-00973-1, published online 6 Decemb...

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

Abstract

Extracted data

Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

Abstract

Extracted data

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