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Genetics

D-Index
64
Citations
14935
World Ranking
2791
National Ranking
1223

Overview

Ranjan Deka is affiliated with the University of Cincinnati in the United States. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, with significant contributions also in Medicine. Within these broader areas, the main subfields include Genetics, Molecular Biology, Health, Toxicology and Mutagenesis, Physiology, and Pediatrics, Perinatology and Child Health.

The scientist's work covers several focused research topics. These include:

  • Genetic Associations and Epidemiology
  • Birth, Development, and Health
  • Telomeres, Telomerase, and Senescence
  • Toxic Organic Pollutants Impact
  • Single-cell and spatial transcriptomics
  • Epigenetics and DNA Methylation
  • Obesity, Physical Activity, Diet

Ranjan Deka has contributed to a number of scientific publications, including the following recent papers:

  • "Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential," 2022, Science Advances
  • "Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed," 2022, Cell Genomics
  • "A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes," 2022, The Journal of Experimental Medicine
  • "Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing," 2023, Nature Genetics
  • "Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program," 2021, Genome Medicine

The most frequent publication venues for their work include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Journal of Human Genetics
  • Human Genetics and Genomics Advances
  • Science Advances

Deka has collaborated recurrently with several co-authors, including:

  • Daniel E. Weeks
  • Ryan L. Minster
  • Nicola L. Hawley
  • Stephen T. McGarvey
  • Muagututi'a Sefuiva Reupena

Best Publications

  • Estimating African American admixture proportions by use of population-specific alleles.

    Esteban J. Parra;Amy Marcini;Joshua Akey;Jeremy Martinson

  • Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age

    Bing Su;Junhua Xiao;Peter Underhill;Ranjan Deka

  • Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study.

    Daniel Woo;Laura R. Sauerbeck;Brett M. Kissela;Jane C. Khoury

  • RELATIVE MUTATION RATES AT DI-, TRI-, AND TETRANUCLEOTIDE MICROSATELLITE LOCI

    Ranajit Chakraborty;Marek Kimmel;David N. Stivers;Leslea J. Davison

  • Genetic evidence supports demic diffusion of Han culture

    Bo Wen;Hui Li;Daru Lu;Xiufeng Song

  • Ethnic-affiliation estimation by use of population-specific DNA markers.

    Mark D. Shriver;Michael W. Smith;Li Jin;Amy Marcini

  • A NOVEL MEASURE OF GENETIC DISTANCE FOR HIGHLY POLYMORPHIC TANDEM REPEAT LOCI

    M D Shriver;L Jin;E Boerwinkle;R Deka

  • Y chromosome haplotypes reveal prehistorical migrations to the Himalayas.

    Bing Su;Chunjie Xiao;Chunjie Xiao;Ranjan Deka;Mark T. Seielstad

  • African origin of modern humans in East Asia: a tale of 12,000 Y chromosomes.

    Yuehai Ke;Bing Su;Bing Su;Bing Su;Xiufeng Song;Daru Lu

  • Biology, Cytogenetics, and Sensitivity to Immunological Effector Cells of New Head and Neck Squamous Cell Carcinoma Lines

    D S Heo;C Snyderman;S M Gollin;S Pan

  • Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage

    Daniel Woo;Guido J. Falcone;Guido J. Falcone;William J. Devan;William J. Devan;W. Mark Brown

  • A thrifty variant in CREBRF strongly influences body mass index in Samoans.

    Ryan L Minster;Nicola L Hawley;Chi-Ting Su;Chi-Ting Su;Guangyun Sun

  • Polynesian origins: Insights from the Y chromosome

    Bing Su;Li Jin;Li Jin;Peter Underhill;Jeremy Martinson

  • Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations.

    R. Deka;Li Jin;M. D. Shriver;L. M. Yu

  • Inbreeding and risk of late onset complex disease

    Igor Rudan;Diana Rudan;Harry Campbell;Andrew Carothers

  • Measuring european population stratification with microarray genotype data

    Marc Bauchet;Brian McEvoy;Laurel N. Pearson;Ellen E. Quillen

  • Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

    Xihao Li;Zilin Li;Hufeng Zhou;Sheila M Gaynor

  • Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm

    Janice L. Farlow;Hai Lin;Laura Sauerbeck;Dongbing Lai

  • Expanding Southwest Pacific Mitochondrial Haplogroups P and Q

    Jonathan Friedlaender;Theodore Schurr;Fred Gentz;George Koki

  • Genome amplification of single sperm using multiple displacement amplification

    Zhengwen Jiang;Xingqi Zhang;Ranjan Deka;Li Jin

Frequent Co-Authors

Ranajit Chakraborty
Ranajit Chakraborty University of North Texas Health Science Center
Daniel E. Weeks
Daniel E. Weeks University of Pittsburgh
Li Jin
Li Jin Fudan University
Robert E. Ferrell
Robert E. Ferrell University of Pittsburgh
Joseph P. Broderick
Joseph P. Broderick University of Cincinnati
Mark D. Shriver
Mark D. Shriver Pennsylvania State University
Lisa J. Martin
Lisa J. Martin Cincinnati Children's Hospital Medical Center
Dawn Kleindorfer
Dawn Kleindorfer University of Cincinnati
Bing Su
Bing Su Chinese Academy of Sciences
Brett M. Kissela
Brett M. Kissela University of Cincinnati

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