Leppert, Mark F.
University of North Carolina at Chapel Hill · The University of Texas MD Anderson Cancer Center · University of Colorado Boulder · Washington University in St. Louis · University of Utah · Brown University
10 papers on CoChat
Most cited papers
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The International HapMap Project
†The International HapMap Consortium, Genotyping centres: Baylor College of Medicine and ParAllele BioScience, Gibbs, R. A., Belmont, J. W., Hardenbol, P., Willis, T. D., Yu, F., Chinese HapMap Consortium, Yang, H., Ch'ang, L.-Y., et al. (2003) · Nature
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 6,057
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A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy
Allikmets, R., Singh, N., Sun, H., Shroyer, N. F., Hutchinson, A., Chidambaram, A., Gerrard, B., Baird, L., Stauffer, D., Peiffer, A., et al. (1997) · Nature Genetics
Retinal Development and DisordersRetinal Diseases and Treatments
Cited by 1,435
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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
Singh, N. A., Charlier, C., Stauffer, D., DuPont, B. R., Leach, R. J., Melis, R., Ronen, G. M., Bjerre, I., Quattlebaum, T., Murphy, J. V., et al. (1998) · Nature Genetics
Ion channel regulation and functionEpilepsy research and treatment
Cited by 1,199
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Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
Ewart, A. K., Morris, C. A., Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A. D., Leppert, M., & Keating, M. T. (1993) · Nature Genetics
Williams Syndrome ResearchConnective tissue disorders research
Cited by 1,138
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A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes
Cargill, M., Schrodi, S. J., Chang, M., Garcia, V. E., Brandon, R., Callis, K. P., Matsunami, N., Ardlie, K. G., Civello, D., Catanese, J. J., et al. (2007) · The American Journal of Human Genetics
Psoriasis: Treatment and PathogenesisGenetic Associations and Epidemiology
Cited by 1,086
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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics
Williams, R. R., Hunt, S. C., Schumacher, M. C., Hegele, R. A., Leppert, M. F., Ludwig, E. H., & Hopkins, P. N. (1993) · The American Journal of Cardiology
Lipoproteins and Cardiovascular HealthLipid metabolism and disorders
Cited by 566
- Verified
Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD
Saccone, N. L., Culverhouse, R. C., Schwantes-An, T.-H., Cannon, D. S., Chen, X., Cichon, S., Giegling, I., Han, S., Han, Y., Keskitalo-Vuokko, K., et al. (2010) · PLoS Genetics
Smoking Behavior and CessationGenetic Associations and Epidemiology
Cited by 395
- Verified
A Candidate Gene Approach Identifies the CHRNA5-A3-B4 Region as a Risk Factor for Age-Dependent Nicotine Addiction
Weiss, R. B., Baker, T. B., Cannon, D. S., von Niederhausern, A., Dunn, D. M., Matsunami, N., Singh, N. A., Baird, L., Coon, H., McMahon, W. M., et al. (2008) · PLoS Genetics
Smoking Behavior and CessationGenetic Associations and Epidemiology
Cited by 271
- Verified
A high-density SNP genome-wide linkage scan in a large autism extended pedigree
Allen-Brady, K., Miller, J., Matsunami, N., Stevens, J., Block, H., Farley, M., Krasny, L., Pingree, C., Lainhart, J., Leppert, M., et al. (2009) · Molecular Psychiatry
Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology
Cited by 77
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Increased Genetic Vulnerability to Smoking at CHRNA5 in Early-Onset Smokers
Hartz, S. M., Short, S. E., Saccone, N. L., Culverhouse, R., Chen, L., Schwantes-An, T.-H., Coon, H., Han, Y., Stephens, S. H., Sun, J., et al. (2012) · Archives of General Psychiatry
Smoking Behavior and CessationGenetic Associations and Epidemiology
Cited by 75
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