Bulent Ataman

harvard university medical affiliates

H指数:15

被引数:2,792

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Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder

SCIENTIFIC REPORTS

IF3.9

2020-08-2015

OAAI

Using Whole-Exome Sequencing to Identify Inherited Causes of Autism

NEURON

IF15

2013-01-01395

OAAI

Yu, Timothy W.; Chahrour, Maria H.; Coulter, Michael E.; Jiralerspong, Sarn; Okamura-Ikeda, Kazuko; Ataman, Bulent; Schmitz-Abe, Klaus; Harmin, David A.; Adli, Mazhar; Malik, Athar N.; D'Gama, Alissa M.; Lim, Elaine T.; Sanders, Stephan J.; Mochida, Ganesh H.; Partlow, Jennifer N.; Sunu, Christine M.; Felie, Jillian M.; Rodriguez, Jacqueline; Nasir, Ramzi H.; Ware, Janice; Joseph, Robert M.; Hill, R. Sean; Kwan, Benjamin Y.; Al-Saffar, Muna; Mukaddes, Nahit M.; Hashmi, Asif; Balkhy, Soher; Gascon, Generoso G.; Hisama, Fuki M.; LeClair, Elaine; Poduri, Annapurna; Oner, Ozgur; Al-Saad, Samira; Al-Awadi, Sadika A.; Bastaki, Laila; Ben-Omran, Tawfeg; Teebi, Ahmad S.; Al-Gazali, Lihadh; Eapen, Valsamma; Stevens, Christine R.; Rappaport, Leonard; Gabriel, Stacey B.; Markianos, Kyriacos; State, Matthew W.; Greenberg, Michael E.; Taniguchi, Hisaaki; Braverman, Nancy E.; Morrow, Eric M.; Walsh, Christopher A.

Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism

PLOS GENETICS

IF3.7

2012-04-12169

OAAI

Rapid activity-dependent modifications in synaptic structure and function require bidirectional Wnt signaling

NEURON

IF15

2008-03-01268