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Author/Creator Zarrei, Mehdi

1. A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome. Issue 5 (3rd April 2017)

Authors:
Zarrei, Mehdi; Merico, Daniele; Kellam, Barbara; Engchuan, Worrawat; Scriver, Tara; Jokhan, Rikash; Wilson, Michael D.; Parr, Jeremy; Lemire, Edmond G.; Stavropoulos, Dimitri J.; Scherer, Stephen W.
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 5(2017)
Page Start:
1287
Record Type:
Journal Article
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2. Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015). (July 2016)

Authors:
Shay, Jerry; Homma, Noriko; Zhou, Ruyun; Naseer, Muhammad; Chaudhary, Adeel; Al-Qahtani, Mohammed; Hirokawa, Nobutaka; Goudarzi, Maryam; Fornace, Albert; Baeesa, Saleh; Hussain, Deema; Bangash, Mohammed; Alghamdi, Fahad; Schulten, Hans-Juergen; Carracedo, Angel; Khan, Ishaq; Qashqari, Hanadi; Mad...
Journal:
BMC genomics
Issue:
Volume 17:Number 6(2016)
Page Start:
1
Record Type:
Journal Article
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3. Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta‐analysis. Issue 1 (20th November 2017)

Authors:
Zhang, Yanqing; Liu, Yi; Zarrei, Mehdi; Tong, Winnie; Dong, Rui; Wang, Ying; Zhang, Haiyan; Yang, Xiaomeng; MacDonald, Jeffrey R.; Uddin, Mohammed; Scherer, Stephen W.; Gai, Zhongtao
Journal:
American journal of medical genetics
Issue:
Volume 177:Issue 1(2018)
Page Start:
93
Record Type:
Journal Article
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4. Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes. Issue 1 (15th November 2021)

Authors:
Costa, Claudia Ismania Samogy; da Silva Montenegro, Eduarda Morgana; Zarrei, Mehdi; de Sá Moreira, Eloísa; Silva, Isabela Maya Wahys; de Oliveira Scliar, Marília; Wang, Jaqueline Yu Ting; Zachi, Elaine Cristina; Branco, Elisa Varella; da Costa, Silvia Souza; Lourenço, Naila Cristina Vilaça; Viann...
Journal:
Clinical genetics
Issue:
Volume 101:Issue 1(2022)
Page Start:
134
Record Type:
Journal Article
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5. Meta‐Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort. Issue 2 (6th November 2019)

Authors:
da Silva Montenegro, Eduarda Morgana; Costa, Claudia Samogy; Campos, Gabriele; Scliar, Marília; de Almeida, Tatiana Ferreira; Zachi, Elaine Cristina; Silva, Isabela Maya Wahys; Chan, Ada J. S.; Zarrei, Mehdi; Lourenço, Naila C. V.; Yamamoto, Guilherme Lopes; Scherer, Stephen; Passos‐Bueno, Maria ...
Journal:
Autism research
Issue:
Volume 13:Issue 2(2020)
Page Start:
199
Record Type:
Journal Article
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6. Microcephaly‐capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing. Issue 11 (17th August 2016)

Authors:
Naseer, Muhammad Imran; Sogaty, Sameera; Rasool, Mahmood; Chaudhary, Adeel G.; Abutalib, Yousif Ahmed; Walker, Susan; Marshall, Christian R.; Merico, Daniele; Carter, Melissa T.; Scherer, Stephen W.; Al‐Qahtani, Mohammad H.; Zarrei, Mehdi
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 11(2016)
Page Start:
3018
Record Type:
Journal Article
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7. Rare copy number variation in extremely impulsively violent males. (3rd December 2018)

Authors:
Vevera, Jan; Zarrei, Mehdi; Hartmannová, Hana; Jedličková, Ivana; Mušálková, Dita; Přistoupilová, Anna; Oliveriusová, Petra; Trešlová, Helena; Nosková, Lenka; Hodaňová, Kateřina; Stránecký, Viktor; Jiřička, Václav; Preiss, Marek; Příhodová, Kateřina; Šaligová, Jana; Wei, John; Woodbury‐Smith, Mar...
Journal:
Genes, brain, and behavior
Issue:
Volume 18:Number 6(2019)
Page Start:
n/a
Record Type:
Journal Article
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9. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees. Issue 5 (6th May 2020)

Authors:
Woodbury‐Smith, Marc; Zarrei, Mehdi; Wei, John; Thiruvahindrapuram, Bhooma; O'Connor, Irene; Paterson, Andrew D.; Yuen, Ryan K. C.; Dastan, Jila; Stavropoulos, Dimitri J.; Howe, Jennifer L.; Thompson, Ann; Parlier, Morgan; Fernandez, Bridget; Piven, Joseph; Anagnostou, Evdokia; Scherer, Stephen W...
Journal:
American journal of medical genetics
Issue:
Volume 183:Issue 5(2020)
Page Start:
268
Record Type:
Journal Article
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10. Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation. Issue 1 (December 2016)

Authors:
Gazzellone, Matthew; Zarrei, Mehdi; Burton, Christie; Walker, Susan; Uddin, Mohammed; Shaheen, S.; Coste, Julie; Rajendram, Rageen; Schachter, Reva; Colasanto, Marlena; Hanna, Gregory; Rosenberg, David; Soreni, Noam; Fitzgerald, Kate; Marshall, Christian; Buchanan, Janet; Merico, Daniele; Arnold,...
Journal:
Journal of neurodevelopmental disorders
Issue:
Volume 8:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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