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

Bằng Srivastava, Anand K., Schwartz, Charles E.
Được phát hành 2014

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

Bằng Teng, Shaolei, Srivastava, Anand K, Wang, Liangjiang
Được phát hành 2010

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

Bằng Wang, Liangjiang, Srivastava, Anand K, Schwartz, Charles E
Được phát hành 2010

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

Bằng Gudenas, Brian L., Srivastava, Anand K., Wang, Liangjiang
Xuất bản năm PLoS One (2017)

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

Bằng Guzauskas, Gregory F., Ukadike, Kennedy, Rimsky, Lynn, Srivastava, Anand K.
Được phát hành 2007

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

Bằng Cogill, Steven B., Srivastava, Anand K., Yang, Mary Qu, Wang, Liangjiang
Xuất bản năm BMC Syst Biol (2018)

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

Bằng Teng, Shaolei, Wang, Liangjiang, Srivastava, Anand K., Schwartz, Charles E., Alexov, Emil
Được phát hành 2011

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

Bằng Roy, Manas P., Mohan, Uday, Singh, Shivendra K., Singh, Vijay K., Srivastava, Anand K.
Được phát hành 2013

AGTR2 in Brain Development and Function

Bằng Vervoort, Virginie S., Guzauskas, Greagory, Archie, John, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.
Được phát hành 2006

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

Bằng Griggs, Bradley L, Ladd, Sydney, Saul, Robert A, DuPont, Barbara R, Srivastava, Anand K
Được phát hành 2007

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

Bằng Griggs, Bradley L, Ladd, Sydney, Decker, Amy, DuPont, Barbara R, Asamoah, Alexander, Srivastava, Anand K
Được phát hành 2009

Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice

Bằng Rao, Nalini R., Abad, Clemer, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
Xuất bản năm Biology (Basel) (2017)

UBE2A-Related X-linked Intellectual Disability

Bằng Stevenson, Roger E., Chudley, Albert E., Srivastava, Anand K., Rodriguez, Jayson, Friez, Michael J., Schwartz, Charles E.
Xuất bản năm Clin Dysmorphol (2019)

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

Bằng Liu, Ying F., Sowell, Sarah M., Luo, Yue, Chaubey, Alka, Cameron, Richard S., Kim, Hyung-Goo, Srivastava, Anand K.
Xuất bản năm PLoS One (2015)

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

Bằng Carmona-Mora, Paulina, Canales, Cesar P., Cao, Lei, Perez, Irene C., Srivastava, Anand K., Young, Juan I., Walz, Katherina
Được phát hành 2012

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

Bằng Pawlowski, Traci L., Heringer-Walther, Silvia, Cheng, Chun-Huai, Archie, John G., Chen, Chin-Fu, Walther, Thomas, Srivastava, Anand K.
Được phát hành 2009

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

Bằng 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
Được phát hành 2008

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

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

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

Bằng 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
Xuất bản năm PLoS One (2018)

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

Bằng 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.
Xuất bản năm Mol Syndromol (2015)