Intellectual Disability and Autism Spectrum Disorders: Causal Genes and Molecular Mechanisms

著者: Srivastava, Anand K., Schwartz, Charles E.
出版事項 2014

Sequence feature-based prediction of protein stability changes upon amino acid substitutions

著者: Teng, Shaolei, Srivastava, Anand K, Wang, Liangjiang
出版事項 2010

Microarray data integration for genome-wide analysis of human tissue-selective gene expression

著者: Wang, Liangjiang, Srivastava, Anand K, Schwartz, Charles E
出版事項 2010

Integrative genomic analyses for identification and prioritization of long non-coding RNAs associated with autism

著者: Gudenas, Brian L., Srivastava, Anand K., Wang, Liangjiang
出版年 PLoS One (2017)

tSNP-based identification of allelic-loss of gene expression in a patient with a balanced chromosomal rearrangement

著者: Guzauskas, Gregory F., Ukadike, Kennedy, Rimsky, Lynn, Srivastava, Anand K.
出版事項 2007

Co-expression of long non-coding RNAs and autism risk genes in the developing human brain

著者: Cogill, Steven B., Srivastava, Anand K., Yang, Mary Qu, Wang, Liangjiang
出版年 BMC Syst Biol (2018)

Structural Assessment of the Effects of Amino Acid Substitutions on Protein Stability and Protein-Protein Interaction

著者: Teng, Shaolei, Wang, Liangjiang, Srivastava, Anand K., Schwartz, Charles E., Alexov, Emil
出版事項 2011

Determinants of Utilization of Antenatal Care Services in Rural Lucknow, India

著者: Roy, Manas P., Mohan, Uday, Singh, Shivendra K., Singh, Vijay K., Srivastava, Anand K.
出版事項 2013

AGTR2 in Brain Development and Function

著者: Vervoort, Virginie S., Guzauskas, Greagory, Archie, John, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.
出版事項 2006

Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities

著者: Griggs, Bradley L, Ladd, Sydney, Saul, Robert A, DuPont, Barbara R, Srivastava, Anand K
出版事項 2007

Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus

著者: Griggs, Bradley L, Ladd, Sydney, Decker, Amy, DuPont, Barbara R, Asamoah, Alexander, Srivastava, Anand K
出版事項 2009

Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice

著者: Rao, Nalini R., Abad, Clemer, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
出版年 Biology (Basel) (2017)

UBE2A-Related X-linked Intellectual Disability

著者: Stevenson, Roger E., Chudley, Albert E., Srivastava, Anand K., Rodriguez, Jayson, Friez, Michael J., Schwartz, Charles E.
出版年 Clin Dysmorphol (2019)

Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment

著者: Liu, Ying F., Sowell, Sarah M., Luo, Yue, Chaubey, Alka, Cameron, Richard S., Kim, Hyung-Goo, Srivastava, Anand K.
出版年 PLoS One (2015)

RAI1 Transcription Factor Activity Is Impaired in Mutants Associated with Smith-Magenis Syndrome

著者: Carmona-Mora, Paulina, Canales, Cesar P., Cao, Lei, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
出版事項 2012

Candidate Agtr2 influenced genes and pathways identified by expression profiling in the developing brain of Agtr2(−)(/y) mice

著者: Pawlowski, Traci L., Heringer-Walther, Silvia, Cheng, Chun-Huai, Archie, John G., Chen, Chin-Fu, Walther, Thomas, Srivastava, Anand K.
出版事項 2009

Evidence that SIZN1 is a Candidate X-Linked Mental Retardation Gene

著者: Cho, Ginam, Bhat, Shambhu S, Gao, Jinsong, Collins, Julianne S, Rogers, R. Curtis, Simensen, Richard J, Schwartz, Charles E, Golden, Jeffrey A, Srivastava, Anand K
出版事項 2008

Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature

著者: Dukes-Rimsky, Lynn, Guzauskas, Gregory F., Holden, Kenton R., Griggs, Rachel, Ladd, Sydney, del Carmen Montoya, Maria, DuPont, Barbara R., Srivastava, Anand K.
出版事項 2011

Neurodevelopmental disorder-associated ZBTB20 gene variants affect dendritic and synaptic structure

著者: Jones, Kelly A., Luo, Yue, Dukes-Rimsky, Lynn, Srivastava, Deepak P., Koul-Tewari, Richa, Russell, Theron A., Shapiro, Lauren P., Srivastava, Anand K., Penzes, Peter
出版年 PLoS One (2018)

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

著者: Vieira, Gustavo H., Cook, Melissa M., Ferreira De Lima, Renata L., Frigério Domingues, Carlos E., de Carvalho, Daniel R., Soares de Paiva, Isaias, Moretti-Ferreira, Danilo, Srivastava, Anand K.
出版年 Mol Syndromol (2015)