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

Por Srivastava, Anand K., Schwartz, Charles E.
Publicado em 2014

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

Por Teng, Shaolei, Srivastava, Anand K, Wang, Liangjiang
Publicado em 2010

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

Por Wang, Liangjiang, Srivastava, Anand K, Schwartz, Charles E
Publicado em 2010

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

Por Guzauskas, Gregory F., Ukadike, Kennedy, Rimsky, Lynn, Srivastava, Anand K.
Publicado em 2007

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

Por Teng, Shaolei, Wang, Liangjiang, Srivastava, Anand K., Schwartz, Charles E., Alexov, Emil
Publicado em 2011

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

Por Roy, Manas P., Mohan, Uday, Singh, Shivendra K., Singh, Vijay K., Srivastava, Anand K.
Publicado em 2013

AGTR2 in Brain Development and Function

Por Vervoort, Virginie S., Guzauskas, Greagory, Archie, John, Schwartz, Charles E., Stevenson, Roger E., Srivastava, Anand K.
Publicado em 2006

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

Por Griggs, Bradley L, Ladd, Sydney, Saul, Robert A, DuPont, Barbara R, Srivastava, Anand K
Publicado em 2007

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

Por Griggs, Bradley L, Ladd, Sydney, Decker, Amy, DuPont, Barbara R, Asamoah, Alexander, Srivastava, Anand K
Publicado em 2009

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

Por Liu, Ying F., Sowell, Sarah M., Luo, Yue, Chaubey, Alka, Cameron, Richard S., Kim, Hyung-Goo, Srivastava, Anand K.
Publicado no PLoS One (2015)

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

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

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

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

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

Por 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
Publicado em 2008

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

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

Clinical and Molecular Heterogeneity in Brazilian Patients with Sotos Syndrome

Por 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.
Publicado no Mol Syndromol (2015)

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous dom...

Por Srivastava, Anand K., Pispa, Johanna, Hartung, Andrew J., Du, Yangzhu, Ezer, Sini, Jenks, Ted, Shimada, Tokihiko, Pekkanen, Maija, Mikkola, Marja L., Ko, Minoru S. H., Thesleff, Irma, Kere, Juha, Schlessinger, David
Publicado em 1997

Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption

Por Lee, Mi-Hye, Lu, Kangmo, Hazard, Star, Yu, Hongwei, Shulenin, Sergey, Hidaka, Hideki, Kojima, Hideto, Allikmets, Rando, Sakuma, Nagahiko, Pegoraro, Rosemary, Srivastava, Anand K., Salen, Gerald, Dean, Michael, Patel, Shailendra B.
Publicado em 2001

Alterations in CDH15 and KIRREL3 in Patients with Mild to Severe Intellectual Disability

Por Bhalla, Kavita, Luo, Yue, Buchan, Tim, Beachem, Michael A., Guzauskas, Gregory F., Ladd, Sydney, Bratcher, Shelly J., Schroer, Richard J., Balsamo, Janne, DuPont, Barbara R., Lilien, Jack, Srivastava, Anand K.
Publicado em 2008

Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith–Magenis syndrome

Por Vieira, Gustavo H, Rodriguez, Jayson D, Carmona-Mora, Paulina, Cao, Lei, Gamba, Bruno F, Carvalho, Daniel R, de Rezende Duarte, Andréa, Santos, Suely R, de Souza, Deise H, DuPont, Barbara R, Walz, Katherina, Moretti-Ferreira, Danilo, Srivastava, Anand K
Publicado em 2012

Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans

Por Wu, Ye, Arai, Amy C., Rumbaugh, Gavin, Srivastava, Anand K., Turner, Gillian, Hayashi, Takashi, Suzuki, Erika, Jiang, Yuwu, Zhang, Lilei, Rodriguez, Jayson, Boyle, Jackie, Tarpey, Patrick, Raymond, F. Lucy, Nevelsteen, Joke, Froyen, Guy, Stratton, Mike, Futreal, Andy, Gecz, Jozef, Stevenson, Roger, Schwartz, Charles E., Valle, David, Huganir, Richard L., Wang, Tao
Publicado em 2007