Mark J. Daly


AuthID: R-00J-QY6

Publications Requiring Validation

1
TITLE: Contribution of autosomal rare and de novo variants to sex differences in autism
AUTHORS: Mahmoud Koko; Kyle K Satterstrom; Kyle K Satterstrom; Branko Aleksic; Mykyta Artomov; Mafalda Barbosa; Elisa Benetti; Catalina Betancur; Monica Biscaldi Schafer; Anders D Børglum; Harrison Brand; Alfredo Brusco; Joseph D Buxbaum; Gabriele Campos; Simona Cardaropoli; Diana Carli; Angel Carracedo; Marcus C Y Chan; Andreas G Chiocchetti; Brian H Y Chung; Brett Collins; Ryan L Collins; Edwin H Cook; Hilary Coon; Claudia I S Costa; Michael L Cuccaro; David J Cutler; Mark J Daly; Silvia De Rubeis; Bernie Devlin; Ryan N Doan; Enrico Domenici; Shan Dong; Chiara Fallerini; Montserrat Fernández Prieto; Giovanni Battista Ferrero; Christine M Freitag; Jack M Fu; Jay J Gargus; Sherif Gerges; Elisa Giorgio; Ana Cristina Girardi; Stephen Guter; Emily Hansen Kiss; Gail E Herman; Irva Hertz Picciotto; David M Hougaard; Christina M Hultman; Suma Jacob; Miia Kaartinen; Lambertus Klei; Alexander Kolevzon; Itaru Kushima; So Lun Lee; Terho Lehtimäki; Lindsay Liang; Carla Lintas; Alicia Ljungdahl; Caterina Lo Rizzo; Yunin Ludena; Patricia Maciel ; Behrang Mahjani; Nell Maltman; Marianna Manara; Dara S Manoach; Gal Meiri; Idan Menashe; Judith Miller; Nancy Minshew; Matthew Mosconi; Rachel Nguyen; Norio Ozaki; Aarno Palotie; Mara Parellada; Maria Rita Passos Bueno; Lisa Pavinato; Minshi Peng; Margaret Pericak Vance; Antonio M Persico; Isaac N Pessah; Kaija Puura; Abraham Reichenberg; Alessandra Renieri; Kathryn Roeder; Stephan J Sanders; Sven Sandin; Stephen W Scherer; Sabine Schlitt; Rebecca J Schmidt; Lauren Schmitt; Katja Schneider Momm; Paige M Siper; Laura Sloofman; Moyra Smith; Christine R Stevens; Pål Suren; James S Sutcliffe; John A Sweeney; Michael E Talkowski; Flora Tassone; ...More
PUBLISHED: 2025, SOURCE: American Journal of Human Genetics, VOLUME: 112, ISSUE: 3
INDEXED IN: Scopus CrossRef
2
TITLE: A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy  Full Text
AUTHORS: Mikko Muona; Samuel F Berkovic; Leanne M Dibbens; Karen L Oliver; Snezana Maljevic; Marta A Bayly; Tarja Joensuu; Laura Canafoglia; Silvana Franceschetti; Roberto Michelucci; Salla Markkinen; Sarah E Heron; Michael S Hildebrand; Eva Andermann; Frederick Andermann; Antonio Gambardella; Paolo Tinuper; Laura Licchetta; Ingrid E Scheffer; Chiara Criscuolo; Alessandro Filla; Edoardo Ferlazzo; Jamil Ahmad; Adeel Ahmad; Betul Baykan; Edith Said; Meral Topcu; Patrizia Riguzzi; Mary D King; Cigdem Ozkara; Danielle M Andrade; Bernt A Engelsen; Arielle Crespel; Matthias Lindenau; Ebba Lohmann; Veronica Saletti; João Massano ; Michael Privitera; Alberto J Espay; Birgit Kauffmann; Michael Duchowny; Rikke S Moller; Rachel Straussberg; Zaid Afawi; Bruria Ben Zeev; Kaitlin E Samocha; Mark J Daly; Steven Petrou; Holger Lerche; Aarno Palotie; Anna Elina Lehesjoki; ...More
PUBLISHED: 2015, SOURCE: NATURE GENETICS, VOLUME: 47, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 229

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