Literature DB >> 27474218

ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.

Cyril Mignot1, Marie-Laure Moutard2, Agnès Rastetter3, Lucile Boutaud4,5, Solveig Heide1,3, Thierry Billette2, Diane Doummar2, Catherine Garel6, Alexandra Afenjar1, Aurélia Jacquette1, Didier Lacombe7,8, Alain Verloes9, Christine Bole-Feysot10, Patrick Nitschké11, Cécile Masson11, Anne Faudet1, Fabien Lesne1, Thierry Bienvenu12,13,14,15, Caroline Alby4,5, Tania Attié-Bitach4,5, Christel Depienne16,17, Caroline Nava1,3, Delphine Héron1.   

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Year:  2016        PMID: 27474218     DOI: 10.1093/brain/aww181

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


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  11 in total

1.  Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome.

Authors:  Georgia Vasileiou; Silvia Vergarajauregui; Sabine Endele; Bernt Popp; Christian Büttner; Arif B Ekici; Marion Gerard; Nuria C Bramswig; Beate Albrecht; Jill Clayton-Smith; Jenny Morton; Susan Tomkins; Karen Low; Astrid Weber; Maren Wenzel; Janine Altmüller; Yun Li; Bernd Wollnik; George Hoganson; Maria-Renée Plona; Megan T Cho; Christian T Thiel; Hermann-Josef Lüdecke; Tim M Strom; Eduardo Calpena; Andrew O M Wilkie; Dagmar Wieczorek; Felix B Engel; André Reis
Journal:  Am J Hum Genet       Date:  2018-02-08       Impact factor: 11.025

2.  Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.

Authors:  Timothy J Edwards; Elliott H Sherr; A James Barkovich; Linda J Richards
Journal:  Brain       Date:  2016-11-01       Impact factor: 13.501

3.  Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort.

Authors:  Pleuntje J van der Sluijs; Marieke Joosten; Caroline Alby; Tania Attié-Bitach; Kelly Gilmore; Christele Dubourg; Mélanie Fradin; Tianyun Wang; Evangeline C Kurtz-Nelson; Kaitlyn P Ahlers; Peer Arts; Christopher P Barnett; Myla Ashfaq; Anwar Baban; Myrthe van den Born; Sarah Borrie; Tiffany Busa; Alicia Byrne; Miriam Carriero; Claudia Cesario; Karen Chong; Anna Maria Cueto-González; Jennifer C Dempsey; Karin E M Diderich; Dan Doherty; Stense Farholt; Erica H Gerkes; Svetlana Gorokhova; Lutgarde C P Govaerts; Pernille A Gregersen; Scott E Hickey; Mathilde Lefebvre; Francesca Mari; Jelena Martinovic; Hope Northrup; Melanie O'Leary; Kareesma Parbhoo; Sophie Patrier; Bernt Popp; Fernando Santos-Simarro; Corinna Stoltenburg; Christel Thauvin-Robinet; Elisabeth Thompson; Anneke T Vulto-van Silfhout; Farah R Zahir; Hamish S Scott; Rachel K Earl; Evan E Eichler; Neeta L Vora; Yael Wilnai; Jessica L Giordano; Ronald J Wapner; Jill A Rosenfeld; Monique C Haak; Gijs W E Santen
Journal:  Genet Med       Date:  2022-05-18       Impact factor: 8.864

4.  A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria.

Authors:  Pleuntje J van der Sluijs; Mariëlle Alders; Alexander J M Dingemans; Kareesma Parbhoo; Bregje W van Bon; Jennifer C Dempsey; Dan Doherty; Johan T den Dunnen; Erica H Gerkes; Ilana M Milller; Stephanie Moortgat; Debra S Regier; Claudia A L Ruivenkamp; Betsy Schmalz; Thomas Smol; Kyra E Stuurman; Catherine Vincent-Delorme; Bert B A de Vries; Bekim Sadikovic; Scott E Hickey; Jill A Rosenfeld; Isabelle Maystadt; Gijs W E Santen
Journal:  Genes (Basel)       Date:  2021-08-20       Impact factor: 4.096

Review 5.  The role of ARID1B, a BAF chromatin remodeling complex subunit, in neural development and behavior.

Authors:  Jeffrey J Moffat; Eui-Man Jung; Minhan Ka; Amanda L Smith; Byeong Tak Jeon; Gijs W E Santen; Woo-Yang Kim
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2018-08-24       Impact factor: 5.067

6.  Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.

Authors:  Futoshi Sekiguchi; Yoshinori Tsurusaki; Nobuhiko Okamoto; Keng Wee Teik; Seiji Mizuno; Hiroshi Suzumura; Bertrand Isidor; Winnie Peitee Ong; Muzhirah Haniffa; Susan M White; Mari Matsuo; Kayoko Saito; Shubha Phadke; Tomoki Kosho; Patrick Yap; Manisha Goyal; Lorne A Clarke; Rani Sachdev; George McGillivray; Richard J Leventer; Chirag Patel; Takanori Yamagata; Hitoshi Osaka; Yoshiya Hisaeda; Hirofumi Ohashi; Kenji Shimizu; Keisuke Nagasaki; Junpei Hamada; Sumito Dateki; Takashi Sato; Yasutsugu Chinen; Tomonari Awaya; Takeo Kato; Kougoro Iwanaga; Masahiko Kawai; Takashi Matsuoka; Yoshikazu Shimoji; Tiong Yang Tan; Seema Kapoor; Nerine Gregersen; Massimiliano Rossi; Mathieu Marie-Laure; Lesley McGregor; Kimihiko Oishi; Lakshmi Mehta; Greta Gillies; Paul J Lockhart; Kate Pope; Anju Shukla; Katta Mohan Girisha; Ghada M H Abdel-Salam; David Mowat; David Coman; Ok Hwa Kim; Marie-Pierre Cordier; Kate Gibson; Jeff Milunsky; Jan Liebelt; Helen Cox; Salima El Chehadeh; Annick Toutain; Ken Saida; Hiromi Aoi; Gaku Minase; Naomi Tsuchida; Kazuhiro Iwama; Yuri Uchiyama; Toshifumi Suzuki; Kohei Hamanaka; Yoshiteru Azuma; Atsushi Fujita; Eri Imagawa; Eriko Koshimizu; Atsushi Takata; Satomi Mitsuhashi; Satoko Miyatake; Takeshi Mizuguchi; Noriko Miyake; Naomichi Matsumoto
Journal:  J Hum Genet       Date:  2019-09-17       Impact factor: 3.172

Review 7.  Chromatin Remodeling BAF (SWI/SNF) Complexes in Neural Development and Disorders.

Authors:  Godwin Sokpor; Yuanbin Xie; Joachim Rosenbusch; Tran Tuoc
Journal:  Front Mol Neurosci       Date:  2017-08-03       Impact factor: 5.639

8.  Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.

Authors:  Christel Depienne; Caroline Nava; Boris Keren; Solveig Heide; Agnès Rastetter; Sandrine Passemard; Sandra Chantot-Bastaraud; Marie-Laure Moutard; Pankaj B Agrawal; Grace VanNoy; Joan M Stoler; David J Amor; Thierry Billette de Villemeur; Diane Doummar; Caroline Alby; Valérie Cormier-Daire; Catherine Garel; Pauline Marzin; Sophie Scheidecker; Anne de Saint-Martin; Edouard Hirsch; Christian Korff; Armand Bottani; Laurence Faivre; Alain Verloes; Christine Orzechowski; Lydie Burglen; Bruno Leheup; Joelle Roume; Joris Andrieux; Frenny Sheth; Chaitanya Datar; Michael J Parker; Laurent Pasquier; Sylvie Odent; Sophie Naudion; Marie-Ange Delrue; Cédric Le Caignec; Marie Vincent; Bertrand Isidor; Florence Renaldo; Fiona Stewart; Annick Toutain; Udo Koehler; Birgit Häckl; Celina von Stülpnagel; Gerhard Kluger; Rikke S Møller; Deb Pal; Tord Jonson; Maria Soller; Nienke E Verbeek; Mieke M van Haelst; Carolien de Kovel; Bobby Koeleman; Glen Monroe; Gijs van Haaften; Tania Attié-Bitach; Lucile Boutaud; Delphine Héron; Cyril Mignot
Journal:  Hum Genet       Date:  2017-03-10       Impact factor: 4.132

Review 9.  The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective.

Authors:  Britt Mossink; Moritz Negwer; Dirk Schubert; Nael Nadif Kasri
Journal:  Cell Mol Life Sci       Date:  2020-12-02       Impact factor: 9.261

10.  The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.

Authors:  Pleuntje J van der Sluijs; Sandra Jansen; Samantha A Vergano; Miho Adachi-Fukuda; Yasemin Alanay; Adila AlKindy; Anwar Baban; Allan Bayat; Stefanie Beck-Wödl; Katherine Berry; Emilia K Bijlsma; Levinus A Bok; Alwin F J Brouwer; Ineke van der Burgt; Philippe M Campeau; Natalie Canham; Krystyna Chrzanowska; Yoyo W Y Chu; Brain H Y Chung; Karin Dahan; Marjan De Rademaeker; Anne Destree; Tracy Dudding-Byth; Rachel Earl; Nursel Elcioglu; Ellen R Elias; Christina Fagerberg; Alice Gardham; Blanca Gener; Erica H Gerkes; Ute Grasshoff; Arie van Haeringen; Karin R Heitink; Johanna C Herkert; Nicolette S den Hollander; Denise Horn; David Hunt; Sarina G Kant; Mitsuhiro Kato; Hülya Kayserili; Rogier Kersseboom; Esra Kilic; Malgorzata Krajewska-Walasek; Kylin Lammers; Lone W Laulund; Damien Lederer; Melissa Lees; Vanesa López-González; Saskia Maas; Grazia M S Mancini; Carlo Marcelis; Francisco Martinez; Isabelle Maystadt; Marianne McGuire; Shane McKee; Sarju Mehta; Kay Metcalfe; Jeff Milunsky; Seiji Mizuno; John B Moeschler; Christian Netzer; Charlotte W Ockeloen; Barbara Oehl-Jaschkowitz; Nobuhiko Okamoto; Sharon N M Olminkhof; Carmen Orellana; Laurent Pasquier; Caroline Pottinger; Vera Riehmer; Stephen P Robertson; Maian Roifman; Caroline Rooryck; Fabienne G Ropers; Monica Rosello; Claudia A L Ruivenkamp; Mahmut S Sagiroglu; Suzanne C E H Sallevelt; Amparo Sanchis Calvo; Pelin O Simsek-Kiper; Gabriela Soares; Lucia Solaeche; Fatma Mujgan Sonmez; Miranda Splitt; Duco Steenbeek; Alexander P A Stegmann; Constance T R M Stumpel; Saori Tanabe; Eyyup Uctepe; G Eda Utine; Hermine E Veenstra-Knol; Sunita Venkateswaran; Catheline Vilain; Catherine Vincent-Delorme; Anneke T Vulto-van Silfhout; Patricia Wheeler; Golder N Wilson; Louise C Wilson; Bernd Wollnik; Tomoki Kosho; Dagmar Wieczorek; Evan Eichler; Rolph Pfundt; Bert B A de Vries; Jill Clayton-Smith; Gijs W E Santen
Journal:  Genet Med       Date:  2018-11-08       Impact factor: 8.822

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