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

by Srivastava, Anand K., Schwartz, Charles E.
Published 2014

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

by Teng, Shaolei, Srivastava, Anand K, Wang, Liangjiang
Published 2010

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

by Wang, Liangjiang, Srivastava, Anand K, Schwartz, Charles E
Published 2010

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

by Gudenas, Brian L., Srivastava, Anand K., Wang, Liangjiang
Published in PLoS One (2017)

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

by Guzauskas, Gregory F., Ukadike, Kennedy, Rimsky, Lynn, Srivastava, Anand K.
Published 2007

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

by Cogill, Steven B., Srivastava, Anand K., Yang, Mary Qu, Wang, Liangjiang
Published in BMC Syst Biol (2018)

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

by Teng, Shaolei, Wang, Liangjiang, Srivastava, Anand K., Schwartz, Charles E., Alexov, Emil
Published 2011

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

by Roy, Manas P., Mohan, Uday, Singh, Shivendra K., Singh, Vijay K., Srivastava, Anand K.
Published 2013

AGTR2 in Brain Development and Function

by Vervoort, Virginie S., Guzauskas, Greagory, Archie, John, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.
Published 2006

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

by Griggs, Bradley L, Ladd, Sydney, Saul, Robert A, DuPont, Barbara R, Srivastava, Anand K
Published 2007

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

by Griggs, Bradley L, Ladd, Sydney, Decker, Amy, DuPont, Barbara R, Asamoah, Alexander, Srivastava, Anand K
Published 2009

Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice

by Rao, Nalini R., Abad, Clemer, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
Published in Biology (Basel) (2017)

UBE2A-Related X-linked Intellectual Disability

by Stevenson, Roger E., Chudley, Albert E., Srivastava, Anand K., Rodriguez, Jayson, Friez, Michael J., Schwartz, Charles E.
Published in Clin Dysmorphol (2019)

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

by Liu, Ying F., Sowell, Sarah M., Luo, Yue, Chaubey, Alka, Cameron, Richard S., Kim, Hyung-Goo, Srivastava, Anand K.
Published in PLoS One (2015)

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

by Carmona-Mora, Paulina, Canales, Cesar P., Cao, Lei, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
Published 2012

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

by Pawlowski, Traci L., Heringer-Walther, Silvia, Cheng, Chun-Huai, Archie, John G., Chen, Chin-Fu, Walther, Thomas, Srivastava, Anand K.
Published 2009

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

by 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
Published 2008

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

by Dukes-Rimsky, Lynn, Guzauskas, Gregory F., Holden, Kenton R., Griggs, Rachel, Ladd, Sydney, del Carmen Montoya, Maria, DuPont, Barbara R., Srivastava, Anand K.
Published 2011

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

by 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
Published in PLoS One (2018)

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

by 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.
Published in Mol Syndromol (2015)