Vamsee Pillalamarri

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

Michael E. Talkowski, Jill A. Rosenfeld, Ian Blumenthal et al. · Cell · 2012 · 586 citations · Full text

Developmental Anomaly, Confer Risk, Developmental Biology +12

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L. Collins et al. · Nature Genetics · 2016 · 346 citations · Full text

Human Congenital Anomalies, Developmental Anomaly, Developmental Biology +8

Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample

Michael E. Talkowski, Zehra Ordulu, Vamsee Pillalamarri et al. · New England Journal of Medicine · 2012 · 196 citations · Full text

Genetics, Diagnosis, Pathology +18

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags et al. · Human Molecular Genetics · 2013 · 172 citations · Full text

Astn2/trim32 Locus, Brain Development, Autism Spectrum Disorders +19

Blood-derived mitochondrial DNA copy number is associated with gene expression across multiple tissues and is predictive for incident neurodegenerative disease

Stephanie Yang, Christina A. Castellani, Ryan J. Longchamps et al. · Genome Research · 2021 · 97 citations · Full text

Engineering, Genetics, Genetic Epidemiology +18