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

由 Srivastava, Anand K., Schwartz, Charles E.
出版 2014

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

由 Teng, Shaolei, Srivastava, Anand K, Wang, Liangjiang
出版 2010

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

由 Wang, Liangjiang, Srivastava, Anand K, Schwartz, Charles E
出版 2010

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

由 Gudenas, Brian L., Srivastava, Anand K., Wang, Liangjiang
發表在 PLoS One (2017)

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

由 Guzauskas, Gregory F., Ukadike, Kennedy, Rimsky, Lynn, Srivastava, Anand K.
出版 2007

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

由 Cogill, Steven B., Srivastava, Anand K., Yang, Mary Qu, Wang, Liangjiang
發表在 BMC Syst Biol (2018)

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

由 Teng, Shaolei, Wang, Liangjiang, Srivastava, Anand K., Schwartz, Charles E., Alexov, Emil
出版 2011

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

由 Roy, Manas P., Mohan, Uday, Singh, Shivendra K., Singh, Vijay K., Srivastava, Anand K.
出版 2013

AGTR2 in Brain Development and Function

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

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

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

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

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

Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice

由 Rao, Nalini R., Abad, Clemer, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
發表在 Biology (Basel) (2017)

UBE2A-Related X-linked Intellectual Disability

由 Stevenson, Roger E., Chudley, Albert E., Srivastava, Anand K., Rodriguez, Jayson, Friez, Michael J., Schwartz, Charles E.
發表在 Clin Dysmorphol (2019)

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

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

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

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

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

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

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

由 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 2008

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

由 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 2011

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

由 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
發表在 PLoS One (2018)

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

由 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.
發表在 Mol Syndromol (2015)