All papers authored by William Dobyns
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2023
C. A. P. F. Alves 
,
J. Sidpra ,
A. Manteghinejad ,
S. Sudhakar ,
F. V. Massey ,
K. A. Aldinger ,
P. Haldipur ,
L. T. Lucato ,
S. F. Ferraciolli ,
S. R. Teixeira ,
Ö. Öztekin ,
D. Bhattacharya ,
A. Taranath ,
S. P. Prabhu ,
D. M. Mirsky
and 8 other authors
,
J. Sidpra ,
A. Manteghinejad ,
S. Sudhakar ,
F. V. Massey ,
K. A. Aldinger ,
P. Haldipur ,
L. T. Lucato ,
S. F. Ferraciolli ,
S. R. Teixeira ,
Ö. Öztekin ,
D. Bhattacharya ,
A. Taranath ,
S. P. Prabhu ,
D. M. Mirsky
and 8 other authors
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis
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2022
M. T. Whitehead ,
M. J. Barkovich ,
J. Sidpra ,
C. A. Alves ,
D. M. Mirsky ,
Ö. Öztekin ,
D. Bhattacharya ,
L. T. Lucato ,
S. Sudhakar ,
A. Taranath ,
S. Andronikou ,
S. P. Prabhu ,
K. A. Aldinger ,
P. Haldipur ,
K. J. Millen
and 4 other authors
,
M. J. Barkovich ,
J. Sidpra ,
C. A. Alves ,
D. M. Mirsky ,
Ö. Öztekin ,
D. Bhattacharya ,
L. T. Lucato ,
S. Sudhakar ,
A. Taranath ,
S. Andronikou ,
S. P. Prabhu ,
K. A. Aldinger ,
P. Haldipur ,
K. J. Millen
and 4 other authors
Refining the Neuroimaging Definition of the Dandy-Walker Phenotype
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2020
Rachel Rabin ,
Alireza Radmanesh,
Ian A. Glass,
William B. Dobyns ,
Kimberly A. Aldinger,
Joseph T. Shieh,
Shelby Romoser,
Hannah Bombei,
Leah Dowsett ,
Pamela Trapane,
John A. Bernat ,
Janice Baker,
Nancy J. Mendelsohn,
Bernt Popp,
Manuela Siekmeyer
and 26 other authors
,
Alireza Radmanesh,
Ian A. Glass,
William B. Dobyns ,
Kimberly A. Aldinger,
Joseph T. Shieh,
Shelby Romoser,
Hannah Bombei,
Leah Dowsett ,
Pamela Trapane,
John A. Bernat ,
Janice Baker,
Nancy J. Mendelsohn,
Bernt Popp,
Manuela Siekmeyer
and 26 other authors
Genotype–phenotype correlation at codon 1740 of SETD2
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2019
Pauline Marzin ,
Sophie Rondeau,
Kimberly A. Aldinger ,
Jean‐Luc Alessandri,
Bertrand Isidor,
Delphine Heron,
Boris Keren,
William B. Dobyns ,
Valérie Cormier‐Daire
,
Sophie Rondeau,
Kimberly A. Aldinger ,
Jean‐Luc Alessandri,
Bertrand Isidor,
Delphine Heron,
Boris Keren,
William B. Dobyns ,
Valérie Cormier‐Daire
SETD2 related overgrowth syndrome: Presentation of four new patients and review of the literature
Download from onlinelibrary.wiley.com
Lyse Ruaud ,
Gillian I. Rice ,
Christelle Cabrol,
Juliette Piard ,
Mathieu Rodero ,
Lien van Eyk,
Elise Boucher-Brischoux,
Alain Maertens de Noordhout,
Ricardo Maré,
Emmanuel Scalais,
Fernand Pauly,
François-Guillaume Debray,
William Dobyns ,
Carolina Uggenti,
Ji Woo Park
and 4 other authors
Download from www.research.manchester.ac.uk
,
Gillian I. Rice ,
Christelle Cabrol,
Juliette Piard ,
Mathieu Rodero ,
Lien van Eyk,
Elise Boucher-Brischoux,
Alain Maertens de Noordhout,
Ricardo Maré,
Emmanuel Scalais,
Fernand Pauly,
François-Guillaume Debray,
William Dobyns ,
Carolina Uggenti,
Ji Woo Park
and 4 other authors
Download from www.research.manchester.ac.uk
Andrew E. Fry ,
Katherine A. Fawcett,
Nathanel Zelnik,
Hongjie Yuan,
Belinda A. N. Thompson,
Lilach Shemer-Meiri,
Thomas D. Cushion,
Hood Mugalaasi,
David Sims,
Neil Stoodley,
Seo-Kyung Chung,
Mark I. Rees,
Chirag V. Patel,
Louise A. Brueton,
Valérie Layet
and 26 other authors
,
Katherine A. Fawcett,
Nathanel Zelnik,
Hongjie Yuan,
Belinda A. N. Thompson,
Lilach Shemer-Meiri,
Thomas D. Cushion,
Hood Mugalaasi,
David Sims,
Neil Stoodley,
Seo-Kyung Chung,
Mark I. Rees,
Chirag V. Patel,
Louise A. Brueton,
Valérie Layet
and 26 other authors
De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
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2016
Livia Garavelli,
Ivan Ivanovski ,
Stefano Giuseppe Caraffi ,
Daniela Santodirocco ,
Marzia Pollazzon ,
Duccio Maria Cordelli ,
Ebtesam Abdalla,
Patrizia Accorsi,
Margaret P. Adam ,
Chiara Baldo ,
Allan Bayat ,
Elga Belligni ,
Federico Bonvicini,
Jeroen Breckpot ,
Bert Callewaert
and 44 other authors
,
Stefano Giuseppe Caraffi ,
Daniela Santodirocco ,
Marzia Pollazzon ,
Duccio Maria Cordelli ,
Ebtesam Abdalla,
Patrizia Accorsi,
Margaret P. Adam ,
Chiara Baldo ,
Allan Bayat ,
Elga Belligni ,
Federico Bonvicini,
Jeroen Breckpot ,
Bert Callewaert
and 44 other authors
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients
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