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

od Srivastava, Anand K., Schwartz, Charles E.
Izdano 2014

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

od Teng, Shaolei, Srivastava, Anand K, Wang, Liangjiang
Izdano 2010

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

od Wang, Liangjiang, Srivastava, Anand K, Schwartz, Charles E
Izdano 2010

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

od Gudenas, Brian L., Srivastava, Anand K., Wang, Liangjiang
Izdano u PLoS One (2017)

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

od Guzauskas, Gregory F., Ukadike, Kennedy, Rimsky, Lynn, Srivastava, Anand K.
Izdano 2007

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

od Cogill, Steven B., Srivastava, Anand K., Yang, Mary Qu, Wang, Liangjiang
Izdano u BMC Syst Biol (2018)

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

od Teng, Shaolei, Wang, Liangjiang, Srivastava, Anand K., Schwartz, Charles E., Alexov, Emil
Izdano 2011

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

od Roy, Manas P., Mohan, Uday, Singh, Shivendra K., Singh, Vijay K., Srivastava, Anand K.
Izdano 2013

AGTR2 in Brain Development and Function

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

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

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

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

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

Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice

od Rao, Nalini R., Abad, Clemer, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
Izdano u Biology (Basel) (2017)

UBE2A-Related X-linked Intellectual Disability

od Stevenson, Roger E., Chudley, Albert E., Srivastava, Anand K., Rodriguez, Jayson, Friez, Michael J., Schwartz, Charles E.
Izdano u Clin Dysmorphol (2019)

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

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

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

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

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

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

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

od 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
Izdano 2008

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

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

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

od 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
Izdano u PLoS One (2018)

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

od 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.
Izdano u Mol Syndromol (2015)