World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
55
Citations
13408
World Ranking
3568
National Ranking
1545

Tamim H. Shaikh 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 Tamim H. Shaikh 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: 96 publications — 6th percentile

6% of scientists in this discipline score the same or lower.

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

Tamim H. Shaikh 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 Tamim H. Shaikh 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: 55 D-Index — 19th percentile

19% of scientists in this discipline score the same or lower.

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

Overview

Tamim H. Shaikh is affiliated with the University of Colorado Denver in the United States. Their research primarily spans the field of Biochemistry, Genetics, and Molecular Biology, with significant contributions in related subfields including Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health, and Developmental Neuroscience.

The main topics that Tamim H. Shaikh focuses on include:

  • Genomic variations and chromosomal abnormalities
  • Congenital heart defects research
  • Genomics and Rare Diseases
  • Chromosomal and Genetic Variations
  • Prenatal Screening and Diagnostics
  • Williams Syndrome Research
  • RNA and protein synthesis mechanisms

Tamim H. Shaikh has been actively publishing in various scientific venues. Frequent publication venues include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genetics
  • Frontiers in Genetics
  • Biology Open
  • Developmental Medicine & Child Neurology

Among the recent papers authored or coauthored by Tamim H. Shaikh are:

  • Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation, 2021, Genetics
  • 22q11.2 Low Copy Repeats Expanded in the Human Lineage, 2021, Frontiers in Genetics
  • Abnormal expression of GABAA receptor sub-units and hypomotility upon loss of gabra1 in zebrafish, 2020, Biology Open
  • Whole-exome sequencing and adrenocorticotropic hormone therapy in individuals with infantile spasms, 2021, Developmental Medicine & Child Neurology
  • Genome-wide copy number variations in a large cohort of bantu African children, 2021, BMC Medical Genomics

Tamim H. Shaikh collaborates frequently with several researchers. Notable frequent coauthors include:

  • Feyza Yilmaz
  • Hung-Chun Yu
  • Yulia Mostovoy
  • Elizabeth A. Geiger
  • Curtis R. Coughlin

Best Publications

  • The DNA sequence of human chromosome 22

    I. Dunham;N. Shimizu;B. A. Roe;S. Chissoe

  • Microduplications of 16p11.2 are Associated with Schizophrenia

    Shane E. McCarthy;Vladimir Makarov;George Kirov;Anjene M. Addington

  • A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

    Santhosh Girirajan;Jill A. Rosenfeld;Gregory M. Cooper;Francesca Antonacci

  • Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

    Tamim H. Shaikh;Hiroki Kurahashi;Sulagna C. Saitta;Anna Mizrahy O’Hare

  • Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

    J. Elia;X. Gai;H. M. Xie;J. C. Perin

  • African origin of human-specific polymorphic Alu insertions

    M A Batzer;M Stoneking;M Alegria-Hartman;H Bazan

  • Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies

    Brendan J. Keating;Sam Tischfield;Sam Tischfield;Sarah S. Murray;Tushar Bhangale

  • Copy number variation at 1q21.1 associated with neuroblastoma

    Sharon J. Diskin;Cuiping Hou;Joseph T. Glessner;Edward F. Attiyeh;Edward F. Attiyeh

  • High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

    Tamim H. Shaikh;Xiaowu Gai;Juan C. Perin;Joseph T. Glessner

  • Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.

    Paweł Stankiewicz;Partha Sen;Samarth S. Bhatt;Mekayla Storer

  • Segmental duplications: an 'expanding' role in genomic instability and disease.

    Beverly S. Emanuel;Tamim H. Shaikh

  • Duplication of 7q34 in pediatric low-grade astrocytomas detected by high-density single-nucleotide polymorphism-based genotype arrays results in a novel BRAF fusion gene.

    Angela J. Sievert;Eric M. Jackson;Xiaowu Gai;Hakon Hakonarson

  • Genomic Analysis Using High-Density Single Nucleotide Polymorphism-Based Oligonucleotide Arrays and Multiplex Ligation-Dependent Probe Amplification Provides a Comprehensive Analysis of INI1/SMARCB1 in Malignant Rhabdoid Tumors

    Eric M. Jackson;Angela J. Sievert;Xiaowu Gai;Hakon Hakonarson

  • Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5.

    Peter R. Baker;Marisa W. Friederich;Michael A. Swanson;Tamim Shaikh

  • Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.

    Pamela Feliciano;Xueya Zhou;Irina Astrovskaya;Tychele N. Turner

  • Structure and variability of recently inserted Alu family members

    Mark A. Batzer;Gail E. Kilroy;Pamela E. Richard;Tamim H. Shaikh

  • Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

    Blake C Ballif;Sara A Hornor;Elizabeth Jenkins;Suneeta Madan-Khetarpal

  • Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome

    Mark C. Hannibal;Kati J. Buckingham;Sarah B. Ng;Jeffrey E. Ming

  • Rare structural variation of synapse and neurotransmission genes in autism

    X Gai;H M Xie;J C Perin;N Takahashi

  • Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development

    Peter M. Van Laarhoven;Leif R. Neitzel;Anita M Quintana;Elizabeth A. Geiger

Frequent Co-Authors

Elaine H. Zackai
Elaine H. Zackai Children's Hospital of Philadelphia
Beverly S. Emanuel
Beverly S. Emanuel Children's Hospital of Philadelphia
Hakon Hakonarson
Hakon Hakonarson Children's Hospital of Philadelphia
Jaclyn A. Biegel
Jaclyn A. Biegel University of Southern California
Xiaowu Gai
Xiaowu Gai Children's Hospital of Los Angeles
Hiroki Kurahashi
Hiroki Kurahashi Fujita Health University
Donna M. McDonald-McGinn
Donna M. McDonald-McGinn Children's Hospital of Philadelphia
Nancy B. Spinner
Nancy B. Spinner Children's Hospital of Philadelphia
Struan F.A. Grant
Struan F.A. Grant University of Pennsylvania
Mark A. Batzer
Mark A. Batzer Louisiana State University

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