World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
70
Citations
13397
World Ranking
2293
National Ranking
1029

David A. Greenberg 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 David A. Greenberg 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: 203 publications — 52nd percentile

52% of scientists in this discipline score the same or lower.

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

David A. Greenberg 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 David A. Greenberg 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: 70 D-Index — 49th percentile

49% of scientists in this discipline score the same or lower.

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

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Statistics

David A. Greenberg mostly deals with Genetics, Locus, Genetic linkage, Internal medicine and Penetrance. His Genetics study combines topics in areas such as Juvenile myoclonic epilepsy and Epilepsy. His research integrates issues of Microsatellite, Allele, Graves' disease and Thyroglobulin in his study of Locus.

His Genetic linkage research is multidisciplinary, relying on both Epistasis and Linkage disequilibrium. His studies deal with areas such as Endocrinology and Immunology as well as Internal medicine. His Penetrance study combines topics from a wide range of disciplines, such as Statistics and Linkage.

His most cited work include:

  • Evidence for a Susceptibility Gene for Autism on Chromosome 2 and for Genetic Heterogeneity (295 citations)
  • Association between a GABRB3 polymorphism and autism. (283 citations)
  • Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6. (256 citations)

What are the main themes of his work throughout his whole career to date?

His primary scientific interests are in Genetics, Locus, Genetic linkage, Internal medicine and Statistics. His research brings together the fields of Juvenile myoclonic epilepsy and Genetics. His research on Locus also deals with topics like

  • Epilepsy and related Proband,
  • Candidate gene and related Genetic determinism.

His Genetic linkage research includes themes of Pedigree chart, Genetic association, Genotype, Gene mapping and Genetic heterogeneity. The concepts of his Internal medicine study are interwoven with issues in Endocrinology, Immunology and Oncology. His Statistics research is multidisciplinary, incorporating elements of Nuclear family and Genetic model.

He most often published in these fields:

  • Genetics (66.81%)
  • Locus (31.44%)
  • Genetic linkage (25.76%)

What were the highlights of his more recent work (between 2008-2021)?

  • Genetics (66.81%)
  • Internal medicine (21.83%)
  • Epilepsy (17.47%)

In recent papers he was focusing on the following fields of study:

His primary areas of study are Genetics, Internal medicine, Epilepsy, Locus and Genome-wide association study. His Allele, Genetic linkage, Single-nucleotide polymorphism, Genetic association and Genetic heterogeneity study are his primary interests in Genetics. His Internal medicine research integrates issues from Endocrinology, Immunology, Oncology and Cardiology.

His studies deal with areas such as Channelopathy and Gene as well as Epilepsy. His study focuses on the intersection of Locus and fields such as Genetic predisposition with connections in the field of Autoimmune thyroiditis. His work in Genome-wide association study addresses issues such as Computational biology, which are connected to fields such as Statistic, Locus heterogeneity and Epistasis.

Between 2008 and 2021, his most popular works were:

  • NOS1AP Is a Genetic Modifier of the Long-QT Syndrome (212 citations)
  • Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4) (156 citations)
  • HLA associations reveal genetic heterogeneity in psoriatic arthritis and in the psoriasis phenotype (145 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Genetics
  • Mutation

His scientific interests lie mostly in Genetics, Internal medicine, Genome-wide association study, Epilepsy and Immunology. His is involved in several facets of Genetics study, as is seen by his studies on Locus, Genetic predisposition, Candidate gene, Genetic association and Single-nucleotide polymorphism. His research investigates the link between Locus and topics such as Genotyping that cross with problems in Breast cancer.

His biological study spans a wide range of topics, including CYP2D6 Gene, Genetic heterogeneity, Endocrinology and Oncology. His work on Genetic linkage expands to the thematically related Epilepsy. His Idiopathic generalized epilepsy study integrates concerns from other disciplines, such as Juvenile myoclonic epilepsy and Myoclonic epilepsy.

Best Publications

  • Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

    Joseph D. Buxbaum;Jeremy M. Silverman;Christopher J. Smith;Mario Kilifarski

  • Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6.

    David A. Greenberg;David A. Greenberg;Antonio V. Delgado-Escueta;Antonio V. Delgado-Escueta;Heidi Widelitz;Robert S. Sparkes

  • Association between a GABRB3 polymorphism and autism.

    Buxbaum Jd;Silverman Jm;Smith Cj;Greenberg Da

  • Linkage analysis of "necessary" disease loci versus "susceptibility" loci.

    Greenberg Da

  • A C/T Single-Nucleotide Polymorphism in the Region of the CD40 Gene is Associated with Graves' Disease

    Yaron Tomer;Erlinda Concepcion;David A. Greenberg

  • Common and Unique Susceptibility Loci in Graves and Hashimoto Diseases: Results of Whole-Genome Screening in a Data Set of 102 Multiplex Families

    Yaron Tomer;Yoshiyuki Ban;Erlinda Concepcion;Giuseppe Barbesino

  • NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

    Lia Crotti;Maria Cristina Monti;Maria Cristina Monti;Roberto Insolia;Anna Peljto

  • BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy

    Deb K. Pal;Oleg V. Evgrafov;Paula Tabares;Fengli Zhang

  • Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

    M. Durner;T. Sander;D. A. Greenberg;K. Johnson

  • Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)

    Lisa J Strug;Tara Clarke;Theodore Chiang;Minchen Chien

  • Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions.

    Yaron Tomer;Giuseppe Barbesino;David A. Greenberg;Erlinda Concepcion

  • Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease.

    Yoshiyuki Ban;David A. Greenberg;Erlinda Concepcion;Lucy Skrabanek

  • HLA associations reveal genetic heterogeneity in psoriatic arthritis and in the psoriasis phenotype

    Robert Winchester;Gregory Minevich;Valeria Steshenko;Brian Kirby

  • Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases.

    Yaron Tomer;David A. Greenberg;Erlinda Concepcion;Yoshiyuki Ban

  • The Power to Detect Linkage in Complex Disease by Means of Simple LOD-Score Analyses

    David A. Greenberg;Paula Abreu;Susan E. Hodge

  • Evidence for Association of Polycystic Ovary Syndrome in Caucasian Women with a Marker at the Insulin Receptor Gene Locus

    Stefania Tucci;Walter Futterweit;Erlinda S. Concepcion;David A. Greenberg

  • CTLA-4 and not CD28 is a susceptibility gene for thyroid autoantibody production.

    Yaron Tomer;David A. Greenberg;Giuseppe Barbesino;Erlinda Concepcion

  • Genome scan of idiopathic generalized epilepsy: evidence for major susceptibility gene and modifying genes influencing the seizure type.

    Martina Durner;Mehdi A. Keddache;Livia Tomasini;Shlomo Shinnar

  • Double bromodomain-containing gene Brd2 is essential for embryonic development in mouse.

    Enyuan Shang;Xiangyuan Wang;Duancheng Wen;David A. Greenberg

  • Arginine at position 74 of the HLA-DR β1 chain is associated with Graves' disease

    Y. Ban;T. F. Davies;D. A. Greenberg;E. S. Concepcion

Frequent Co-Authors

Susan E. Hodge
Susan E. Hodge Columbia University
Yaron Tomer
Yaron Tomer Albert Einstein College of Medicine
Terry F. Davies
Terry F. Davies Icahn School of Medicine at Mount Sinai
Deb K. Pal
Deb K. Pal King's College London
Antonio V. Delgado-Escueta
Antonio V. Delgado-Escueta University of California, Los Angeles
Jeremy M. Silverman
Jeremy M. Silverman Icahn School of Medicine at Mount Sinai
Shlomo Shinnar
Shlomo Shinnar Albert Einstein College of Medicine
Kenneth L. Davis
Kenneth L. Davis Icahn School of Medicine at Mount Sinai
Cynthia L. Harden
Cynthia L. Harden Mount Sinai Beth Israel
Solomon L. Moshé
Solomon L. Moshé Albert Einstein College of Medicine

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Each of these pathways complements a background in genetics and can open up rewarding career opportunities in the thriving healthcare field.

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