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BMC Evolutionary Biology|December 17, 2011
Biophysical and structural considerations for protein sequence evolutionJohan A Grahnen, Priyanka Nandakumar, Jan Kubelka, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 2019
Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung diseaseSumantra Chatterjee, Priyanka Nandakumar, Dallas R Auer, et al.
Medicine|August 17, 2018
Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variationPriyanka Nandakumar, Alanna C Morrison, Megan L Grove, et al.
Science Advances|March 18, 2021
Nuclear genome-wide associations with mitochondrial heteroplasmyPriyanka Nandakumar, Chao Tian, Jared O'Connell, et al.
Plos One|August 4, 2017
MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertensionPriyanka Nandakumar, Adrienne Tin, Megan L Grove, et al.
Journal of Indian Society of Periodontology|March 6, 2023
A comparative study of demineralized freeze-dried bone allograft alone and with 1% metformin in the treatment of intrabony defects in patients with chronic periodontitis: A randomized clinical trialDipika K Mitra, Rutuja Jeevandas Donde, Ankit B Desai, et al.
Scientific Reports|June 21, 2016
Rare coding TTN variants are associated with electrocardiographic QT interval in the general populationAshish Kapoor, Kiranmayee Bakshy, Linda Xu, et al.
Journal of Pediatric Surgery|May 19, 2021
Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjectsAshish Kapoor, Priyanka Nandakumar, Dallas R Auer, et al.
Nature Genetics|November 15, 2016
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variationThomas J Hoffmann, Georg B Ehret, Priyanka Nandakumar, et al.
Human Molecular Genetics|January 13, 2022
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysisHélène Choquet, Weiyu Li, Jie Yin, et al.
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