World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
45
Citations
9489
World Ranking
4217
National Ranking
1818

Andrew C. Lidral 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 Andrew C. Lidral 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: 57 publications — 1st percentile

1% of scientists in this discipline score the same or lower.

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

Andrew C. Lidral 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 Andrew C. Lidral 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: 45 D-Index — 4th percentile

4% of scientists in this discipline score the same or lower.

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

Overview

Andrew C. Lidral is affiliated with the University of Iowa in the United States. Their research spans multiple fields, primarily focusing on biochemistry, genetics, and molecular biology, with significant overlap in medical applications.

The scientist has contributed to various subfields including molecular biology, genetics, surgery, cancer research, and parasitology. Their work frequently centers on neurogenetic and muscular disorders, RNA modifications and cancer, cancer-related gene regulation, congenital diaphragmatic hernia studies, connective tissue disorders, cancer-related molecular mechanisms, and Toxoplasma gondii research.

Andrew C. Lidral has authored several papers published in reputable venues such as American Journal of Medical Genetics Part A, Genes, and UNC Libraries. Notable papers include:

  • CDH1 Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer, 2020, Genes
  • A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature, 2023, American Journal of Medical Genetics Part A
  • Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes, 2020, UNC Libraries
  • Correction to "A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature", 2023, American Journal of Medical Genetics Part A

The scientist collaborates frequently with other researchers, including Jeffrey C. Murray, Timothy C. Cox, Tony Roscioli, Michael F. Buckley, and Alanna Strong.

Research publications indicate a strong focus on genetic mutations associated with orofacial clefting and syndromes involving multiple anomalies. The combination of medical genetics and molecular biology informs their interdisciplinary approach to genetic disorders and developmental anomalies.

Andrew C. Lidral's work contributes to advancing understanding in neurogenetic and muscular disorders as well as molecular mechanisms involved in cancer and congenital conditions.

Best Publications

  • Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

    Shinji Kondo;Brian C. Schutte;Rebecca J. Richardson;Bryan C. Bjork

  • Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

    Theresa M. Zucchero;Margaret E. Cooper;Brion S. Maher;Sandra Daack-Hirsch

  • A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

    Terri H. Beaty;Jeffrey C. Murray;Mary L. Marazita;Ronald G. Munger

  • Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

    Andrew C. Lidral;Paul A. Romitti;Ann M. Basart;Thomas Doetschman

  • Development of the upper lip: morphogenetic and molecular mechanisms.

    Rulang Jiang;Jeffrey O. Bush;Andrew C. Lidral

  • The Role of MSX1 in Human Tooth Agenesis

    A.C. Lidral;B.C. Reising

  • Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35

    Mary L. Marazita;Jeffrey C. Murray;Andrew C. Lidral;Mauricio Arcos-Burgos

  • Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: Evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts

    Paul A. Romitti;Andrew C. Lidral;Ronald G. Munger;Sandra Daack-Hirsch

  • Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines.

    Andrew C. Lidral;Jeffrey C. Murray;Kenneth H. Buetow;Ann M. Basart

  • Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip

    Satoshi Suzuki;Satoshi Suzuki;Mary L. Marazita;Margaret E. Cooper;Nobutomo Miwa

  • Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK.

    Ernst Reichenberger;Valdenize Tiziani;Valdenize Tiziani;Shoji Watanabe;Shoji Watanabe;Lucy Park

  • A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13

    Elizabeth J Leslie;Jenna C Carlson;John R Shaffer;Eleanor Feingold

  • Genetic Association Studies of Cleft Lip and/or Palate With Hypodontia Outside the Cleft Region

    Rebecca L. Slayton;Laura Williams;Jeffrey C. Murray;James J. Wheeler

  • FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

    Lina M. Moreno;Maria Adela Mansilla;Steve A. Bullard;Margaret E. Cooper

  • TBX22 mutations are a frequent cause of cleft palate

    A C B Marçano;K Doudney;C Braybrook;R Squires

  • Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci

    Elizabeth J. Leslie;Margaret A. Taub;Huan Liu;Huan Liu;Karyn Meltz Steinberg

  • Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results.

    Mary L. Marazita;Andrew C. Lidral;Jeffrey C. Murray;L.Leigh Field

  • A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

    Elizabeth J. Leslie;Huan Liu;Huan Liu;Jenna C. Carlson;John R. Shaffer

  • Progress toward discerning the genetics of cleft lip

    Andrew C Lidral;Lina M Moreno

  • Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice.

    Yu Lan;Rosemary C. Ryan;Zunyi Zhang;Steven A. Bullard

Frequent Co-Authors

Jeffrey C. Murray
Jeffrey C. Murray University of Iowa
Mary L. Marazita
Mary L. Marazita University of Pittsburgh
Mauricio Arcos-Burgos
Mauricio Arcos-Burgos University of Antioquia
Kaare Christensen
Kaare Christensen University of Southern Denmark
Rolv T. Lie
Rolv T. Lie University of Bergen
Allen J. Wilcox
Allen J. Wilcox National Institutes of Health
Terri H. Beaty
Terri H. Beaty Johns Hopkins University
Tony Roscioli
Tony Roscioli University of New South Wales
Jacqueline T. Hecht
Jacqueline T. Hecht The University of Texas Health Science Center at Houston
Brian C. Schutte
Brian C. Schutte Michigan State University

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