World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
60
Citations
62195
World Ranking
3088
National Ranking
1346

Manuel A. Rivas publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Manuel A. Rivas sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 150 publications — 30th percentile

30% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Manuel A. Rivas D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Manuel A. Rivas sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 60 D-Index — 29th percentile

29% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Overview

Manuel A. Rivas is affiliated with Stanford University in the United States and has contributed extensively to research in the fields of biochemistry, genetics, molecular biology, and medicine. Their work covers a broad spectrum of genetics and molecular biology, with a focus on subfields such as genetics, molecular biology, epidemiology, statistics and probability, and cardiology and cardiovascular medicine.

The primary topics covered in their research include genetic associations and epidemiology, statistical methods and inference, bioinformatics and genomic networks, genomics and rare diseases, gene expression and cancer classification, liver disease diagnosis and treatment, and genetic and phenotypic traits in livestock.

Manuel A. Rivas has published frequently in several venues, most notably:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Genetics
  • PLoS Genetics
  • Nature Communications
  • UNC Libraries

Recent papers authored or co-authored by Manuel A. Rivas include:

  • A cross-population atlas of genetic associations for 220 human phenotypes, 2021, Nature Genetics
  • Genetics of 35 blood and urine biomarkers in the UK Biobank, 2021, Nature Genetics
  • GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background, 2021, eLife
  • Significant sparse polygenic risk scores across 813 traits in UK Biobank, 2022, PLoS Genetics
  • Race, socioeconomic deprivation, and hospitalization for COVID-19 in English participants of a national biobank, 2020, International Journal for Equity in Health

Frequent collaborators in Manuel A. Rivas's research include:

  • Yosuke Tanigawa
  • Robert Tibshirani
  • Trevor Hastie
  • Johanne Marie Justesen
  • Mark J. Daly

Their work often involves integrating complex genetic data to understand human phenotypes and disease risk, utilizing statistical and computational methods in genetics and epidemiology. The focus on polygenic risk scores and cross-population genetic associations reflects an interest in both the broad genetic landscape and specific molecular mechanisms.

Best Publications

  • A framework for variation discovery and genotyping using next-generation DNA sequencing data

    Mark A DePristo;Eric Banks;Ryan Poplin;Kiran V Garimella

  • Analysis of protein-coding genetic variation in 60,706 humans

    Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

    Kristin G. Ardlie;David S. Deluca;Ayellet V. Segrè

  • Transcriptome and genome sequencing uncovers functional variation in humans

    Tuuli Lappalainen;Michael Sammeth;Marc R. Friedländer;Peter A. C. ‘t Hoen

  • A cross-population atlas of genetic associations for 220 human phenotypes

    Saori Sakaue;Masahiro Kanai;Yosuke Tanigawa;Juha Karjalainen

  • Correction: Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases

    Jialiang Yang;Tao Huang;Francesca Petralia;Quan Long

  • The genetic architecture of type 2 diabetes

    Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan

  • Landscape of X chromosome inactivation across human tissues

    Taru Tukiainen;Taru Tukiainen;Alexandra-Chloé Villani;Alexandra-Chloé Villani;Angela Yen;Angela Yen;Manuel A. Rivas;Manuel A. Rivas;Manuel A. Rivas

  • Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.

    Manuel A. Rivas;Manuel A. Rivas;Manuel A. Rivas;Mélissa Beaudoin;Agnes Gardet;Christine Stevens

  • Opportunities and challenges for transcriptome-wide association studies.

    Michael Wainberg;Nasa Sinnott-Armstrong;Nicholas Mancuso;Alvaro N. Barbeira

  • Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

    Ron Do;Ron Do;Nathan O. Stitziel;Hong Hee Won;Hong Hee Won;Anders Berg Jørgensen

  • Testing for an unusual distribution of rare variants.

    Benjamin Michael Neale;Manuel A. Rivas;Manuel A. Rivas;Benjamin F. Voight;Benjamin F. Voight;David Matthew Altshuler;David Matthew Altshuler

  • A map of human genome variation from population-scale sequencing

    Richard M. Durbin;David L. Altshuler;Gonçalo R. Abecasis;David R. Bentley

  • Genetics of 35 blood and urine biomarkers in the UK Biobank

    Nasa Sinnott-Armstrong;Nasa Sinnott-Armstrong;Nasa Sinnott-Armstrong;Yosuke Tanigawa;David Amar;David Amar;Nina Mars

  • Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

    Valérie Turcot;Yingchang Lu;Yingchang Lu;Heather M Highland;Heather M Highland;Claudia Schurmann

  • High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

    Sarah E Calvo;Elena J Tucker;Elena J Tucker;Alison G Compton;Denise M Kirby

  • Effect of predicted protein-truncating genetic variants on the human transcriptome

    Manuel A. Rivas;Matti Pirinen;Donald F. Conrad;Monkol Lek

  • Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer

    Elise Ruark;Katie Snape;Peter Humburg;Chey Loveday

  • The genetic architecture of type 2 diabetes

    Christian Fuchsberger;Jason Flannick;Tanya M. Teslovich;Anubha Mahajan

Frequent Co-Authors

Mark J. Daly
Mark J. Daly Massachusetts General Hospital
David Altshuler
David Altshuler Harvard University
Erik Ingelsson
Erik Ingelsson Stanford University
Benjamin M. Neale
Benjamin M. Neale Harvard University
Cecilia M. Lindgren
Cecilia M. Lindgren University of Oxford
Daniel G. MacArthur
Daniel G. MacArthur Garvan Institute of Medical Research
Andrew P. Morris
Andrew P. Morris University of Liverpool
Paul W. Franks
Paul W. Franks Lund University
Tonu Esko
Tonu Esko University of Tartu

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