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Genetics

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

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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