World's Best Scientists 2026 revealed!
Settara C. Chandrasekharappa

Settara C. Chandrasekharappa

D-Index & Metrics

Genetics

D-Index
67
Citations
30256
World Ranking
2489
National Ranking
1116

Settara C. Chandrasekharappa 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 Settara C. Chandrasekharappa 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: 177 publications — 41st percentile

41% of scientists in this discipline score the same or lower.

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

Settara C. Chandrasekharappa 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 Settara C. Chandrasekharappa 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: 67 D-Index — 43rd percentile

43% of scientists in this discipline score the same or lower.

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

Overview

Settara C. Chandrasekharappa is affiliated with the National Institutes of Health in the United States. Their research primarily focuses on the fields of biochemistry, genetics, and molecular biology, with a significant number of publications in medicine. Within these domains, they have contributed notably to molecular biology, genetics, hematology, oncology, and cancer research.

The scientist's main research topics encompass DNA repair mechanisms, CRISPR and genetic engineering, cancer-related molecular pathways, prenatal screening and diagnostics, carcinogens and genotoxicity assessment, epigenetics and DNA methylation, as well as genetic factors in colorectal cancer.

Chandrasekharappa has contributed to numerous peer-reviewed publications, with frequent appearances in several respected venues. These include bioRxiv (Cold Spring Harbor Laboratory), Blood, Proceedings of the National Academy of Sciences, Blood Advances, and Molecular Case Studies.

Among their recent papers are:

  • Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis, 2020, Proceedings of the National Academy of Sciences
  • Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer, 2022, Nature
  • Association of clinical severity with FANCB variant type in Fanconi anemia, 2020, Blood
  • Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas, 2020, Scientific Reports
  • Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy, 2023, Blood Advances

Chandrasekharappa has collaborated frequently with several co-authors including Frank X. Donovan, Agata Smogorzewska, Francis P. Lach, Arleen D. Auerbach, and Raymond J. Noonan.

Best Publications

  • Mutation in the α-synuclein gene identified in families with Parkinson's disease

    Mihael H. Polymeropoulos;Christian Lavedan;Elisabeth Leroy;Susan E. Ide

  • Positional Cloning of the Gene for Multiple Endocrine Neoplasia-Type 1

    Settara C. Chandrasekharappa;Siradanahalli C. Guru;Pachiappan Manickam;Shodimu Emmanuel Olufemi

  • Mutations in the human Jagged1 gene are responsible for Alagille syndrome

    Takaya Oda;Abdel G. Elkahloun;Brian L. Pike;Kazuki Okajima

  • Mind Bomb Is a Ubiquitin Ligase that Is Essential for Efficient Activation of Notch Signaling by Delta

    Motoyuki Itoh;Cheol-Hee Kim;Gregory Palardy;Takaya Oda

  • Menin Interacts with the AP1 Transcription Factor JunD and Represses JunD-Activated Transcription

    Sunita K. Agarwal;Siradanahalli C. Guru;Christina Heppner;Michael R. Erdos

  • Isolation of a partial candidate gene for Menkes disease by positional cloning.

    Julian F. B. Mercer;Janie Livingston;Bryan Hall;Jennifer A. Paynter

  • Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

    Qing Zhou;Hongying Wang;Daniella M. Schwartz;Monique Stoffels

  • Menin, the product of the MEN1 gene, is a nuclear protein

    Siradanahalli C. Guru;Paul K. Goldsmith;A. Lee Burns;Stephen J. Marx

  • Germline Mutations of the MEN1 Gene in Familial Multiple Endocrine Neoplasia Type 1 and Related States

    Sunita K. Agarwal;Mary Beth Kester;Larisa V. Debelenko;Christina Heppner

  • A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors

    Judy S. Crabtree;Peter Christopher Scacheri;Jerrold M. Ward;Lisa Garrett-Beal

  • Repressor activity of Headless/Tcf3 is essential for vertebrate head formation.

    Cheol-Hee Kim;Takaya Oda;Motoyuki Itoh;Di Jiang

  • Somatic mutation of the MEN1 gene in parathyroid tumours.

    Heppner C;Kester Mb;Agarwal Sk;Debelenko Lv

  • Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.

    Kirk Mykytyn;Darryl Y. Nishimura;Charles C. Searby;Mythreyi Shastri

  • A Novel Putative Low-Affinity Insulin-like Growth Factor-binding Protein, LIBC (Lost in Inflammatory Breast Cancer), and RhoC GTPase Correlate with the Inflammatory Breast Cancer Phenotype

    Kenneth L. Van Golen;Seena Davies;Zhi Fen Wu;Yun Fang Wang

  • Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas

    Zhengping Zhuang;Alexander O. Vortmeyer;Svetlana Pack;Steve Huang

  • The tumor suppressor protein menin interacts with NF-κb proteins and inhibits NF-κb-mediated transactivation

    Christina Heppner;Karl Y. Bilimoria;Sunita K. Agarwal;Mary Beth Kester

  • Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expression.

    Linzhao Cheng;Nancy F. Hansen;Ling Zhao;Yutao Du

  • Mutations of the MEN1 Tumor Suppressor Gene in Pituitary Tumors

    Zhengping Zhuang;Shereen Z. Ezzat;Alexander O. Vortmeyer;Robert Weil

  • Identification of MEN1 Gene Mutations in Sporadic Carcinoid Tumors of the Lung

    Larisa V. Debelenko;Elisabeth Brambilla;Sunita K. Agarwal;Jennifer I. Swalwell

  • Of Mice and MEN1: Insulinomas in a Conditional Mouse Knockout

    Judy S. Crabtree;Peter C. Scacheri;Jerrold M. Ward;Sara R. McNally

Frequent Co-Authors

Francis S. Collins
Francis S. Collins National Institutes of Health
Stephen J. Marx
Stephen J. Marx National Institutes of Health
Allen M. Spiegel
Allen M. Spiegel Albert Einstein College of Medicine
Michael R. Emmert-Buck
Michael R. Emmert-Buck Avoneaux Medical Institute
Lance A. Liotta
Lance A. Liotta George Mason University
Abdel G. Elkahloun
Abdel G. Elkahloun National Human Genome Research Institute
James C. Mullikin
James C. Mullikin National Institutes of Health
Zhengping Zhuang
Zhengping Zhuang National Institutes of Health
Arleen D. Auerbach
Arleen D. Auerbach Rockefeller University
Agata Smogorzewska
Agata Smogorzewska Rockefeller University

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