Massively parallel rare disease genetics

por Burns, Kathleen H, Chakravarti, Aravinda
Publicado 2011

Quantifying and Modeling Birth Order Effects in Autism

por Turner, Tychele, Pihur, Vasyl, Chakravarti, Aravinda
Publicado 2011

Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC)

por Salfati, Elias, Morrison, Alanna C., Boerwinkle, Eric, Chakravarti, Aravinda
Publicado 2015

SNPs and Other Features as They Predispose to Complex Disease: Genome-Wide Predictive Analysis of a Quantitative Phenotype for Hypertension

por Won, Joong-Ho, Ehret, Georg, Chakravarti, Aravinda, Olshen, Richard A.
Publicado 2011

HPASubC: A suite of tools for user subclassification of human protein atlas tissue images

por Cornish, Toby C., Chakravarti, Aravinda, Kapoor, Ashish, Halushka, Marc K.
Publicado 2015

Genome‐wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores

por Zhu, Xiaofeng, Zhu, Luke, Wang, Heming, Cooper, Richard S., Chakravarti, Aravinda
Publicado 2022

Copy Number Variants in Candidate Genes Are Genetic Modifiers of Hirschsprung Disease

por Jiang, Qian, Ho, Yen-Yi, Hao, Li, Nichols Berrios, Courtney, Chakravarti, Aravinda
Publicado 2011

Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation

por Nandakumar, Priyanka, Morrison, Alanna C., Grove, Megan L., Boerwinkle, Eric, Chakravarti, Aravinda
Publicado 2018

A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease

por Chatterjee, Sumantra, Karasaki, Kameko M., Fries, Lauren E., Kapoor, Ashish, Chakravarti, Aravinda
Publicado 2021

Sequence-based correction of barcode bias in massively parallel reporter assays

por Lee, Dongwon, Kapoor, Ashish, Lee, Changhee, Mudgett, Michael, Beer, Michael A., Chakravarti, Aravinda
Publicado 2021

RET enhancer haplotype-dependent remodeling of the human fetal gut development program

por Chatterjee, Sumantra, Fries, Lauren E., Yaacov, Or, Hu, Nan, Berk-Rauch, Hanna E., Chakravarti, Aravinda
Publicado 2023

Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays

por Lin, Shin, Carvalho, Benilton, Cutler, David J, Arking, Dan E, Chakravarti, Aravinda, Irizarry, Rafael A
Publicado 2008

MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension

por Nandakumar, Priyanka, Tin, Adrienne, Grove, Megan L., Ma, Jianzhong, Boerwinkle, Eric, Coresh, Josef, Chakravarti, Aravinda
Publicado 2017

Ret deficiency decreases neural crest progenitor proliferation and restricts fate potential during enteric nervous system development

por Vincent, Elizabeth, Chatterjee, Sumantra, Cannon, Gabrielle H., Auer, Dallas, Ross, Holly, Chakravarti, Aravinda, Goff, Loyal A.
Publicado 2023

Cardiac muscle–restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features

por Smith, Alexa, Auer, Dallas, Johnson, Morgan, Sanchez, Ernesto, Ross, Holly, Ward, Christopher, Chakravarti, Aravinda, Kapoor, Ashish
Publicado 2023

Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa

por Rose, Anna M., Shah, Amna Z., Venturini, Giulia, Krishna, Abhay, Chakravarti, Aravinda, Rivolta, Carlo, Bhattacharya, Shomi S.
Publicado 2016

Human cardiac cis-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants

por Lee, Dongwon, Kapoor, Ashish, Safi, Alexias, Song, Lingyun, Halushka, Marc K., Crawford, Gregory E., Chakravarti, Aravinda
Publicado 2018

Multiple Independent Genetic Factors at NOS1AP Modulate the QT Interval in a Multi-Ethnic Population

por Arking, Dan E., Khera, Amit, Xing, Chao, Kao, W. H. Linda, Post, Wendy, Boerwinkle, Eric, Chakravarti, Aravinda
Publicado 2009

Defining the Contribution of CNTNAP2 to Autism Susceptibility

por Sampath, Srirangan, Bhat, Shambu, Gupta, Simone, O’Connor, Ashley, West, Andrew B., Arking, Dan E., Chakravarti, Aravinda
Publicado 2013

Correction: Defining the Contribution of CNTNAP2 to Autism Susceptibility

por Sampath, Srirangan, Bhat, Shambu, Gupta, Simone, O’Connor, Ashley, West, Andrew B., Arking, Dan E., Chakravarti, Aravinda
Publicado 2013