Weerts, Marjolein J.A. http://orcid.org/0000-0003-1231-1562
Lanko, Kristina
Guzmán-Vega, Francisco J.
Jackson, Adam
Ramakrishnan, Reshmi
Cardona-Londoño, Kelly J.
Peña-Guerra, Karla A.
van Bever, Yolande
van Paassen, Barbara W.
Kievit, Anneke
van Slegtenhorst, Marjon
Allen, Nicholas M.
Kehoe, Caroline M.
Robinson, Hannah K.
Pang, Lewis
Banu, Selina H.
Zaman, Mashaya
Efthymiou, Stephanie
Houlden, Henry
Järvelä, Irma
Lauronen, Leena
Määttä, Tuomo
Schrauwen, Isabelle
Leal, Suzanne M.
Ruivenkamp, Claudia A.L.
Barge-Schaapveld, Daniela Q.C.M.
Peeters-Scholte, Cacha M.P.C.D.
Galehdari, Hamid
Mazaheri, Neda
Sisodiya, Sanjay M.
Harrison, Victoria
Sun, Angela
Thies, Jenny
Pedroza, Luis Alberto
Lara-Taranchenko, Yana
Chinn, Ivan K.
Lupski, James R.
Garza-Flores, Alexandra
McGlothlin, Jeffery
Yang, Lin
Huang, Shaoping
Wang, Xiaodong
Jewett, Tamison
Rosso, Gretchen
Lin, Xi
Mohammed, Shehla
Merritt, J. Lawrence II
Mirzaa, Ghayda M.
Timms, Andrew E.
Scheck, Joshua
Elting, Mariet W.
Polstra, Abeltje M.
Schenck, Lauren
Ruzhnikov, Maura R.Z.
Vetro, Annalisa
Montomoli, Martino
Guerrini, Renzo
Koboldt, Daniel C.
Mosher, Theresa Mihalic
Pastore, Matthew T.
McBride, Kim L.
Peng, Jing
Pan, Zou
Willemsen, Marjolein
Koning, Susanne
Turnpenny, Peter D.
de Vries, Bert B.A.
Gilissen, Christian
Pfundt, Rolph
Lees, Melissa
Braddock, Stephen R.
Klemp, Kara C.
Vansenne, Fleur
van Gijn, Marielle E.
Quindipan, Catherine
Deardorff, Matthew A.
Hamm, J. Austin
Putnam, Abbey M.
Baud, Rebecca
Walsh, Laurence
Lynch, Sally A.
Baptista, Julia
Person, Richard E.
Monaghan, Kristin G.
Crunk, Amy
Keller-Ramey, Jennifer
Reich, Adi
Elloumi, Houda Zghal
Alders, Marielle
Kerkhof, Jennifer
McConkey, Haley
Haghshenas, Sadegheh
Maroofian, Reza
Sadikovic, Bekim
Banka, Siddharth
Arold, Stefan T.
Barakat, Tahsin Stefan
Funding for this research was provided by:
ZonMw (Veni 91617021, Veni 91617021)
Brain and Behavior Research Foundation (NARSAD Young Investigator Grant)
Erasmus Medisch Centrum (Erasmus MC Fellowship 2017)
This article is maintained by: Elsevier
Article Title: Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01246-2
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics