Jorde, Lynn B.
University of Utah
14 papers on CoChatORCID 0000-0002-0606-1862
Most cited papers
- Verified
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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The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Mallick, S., Li, H., Lipson, M., Mathieson, I., Gymrek, M., Racimo, F., Zhao, M., Chennagiri, N., Nordenfelt, S., Tandon, A., et al. (2016) · Nature
Forensic and Genetic ResearchPleistocene-Era Hominins and Archaeology
Cited by 1,584
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Genetic Evidence for High-Altitude Adaptation in Tibet
Simonson, T. S., Yang, Y., Huff, C. D., Yun, H., Qin, G., Witherspoon, D. J., Bai, Z., Lorenzo, F. R., Xing, J., Jorde, L. B., et al. (2010) · Science
High Altitude and HypoxiaForensic and Genetic Research
Cited by 1,227
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Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing
Roach, J. C., Glusman, G., Smit, A. F. A., Huff, C. D., Hubley, R., Shannon, P. T., Rowen, L., Pant, K. P., Goodman, N., Bamshad, M., et al. (2010) · Science
Genomics and Rare DiseasesGenomics and Phylogenetic Studies
Cited by 1,084
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Genetic variation, classification and ‘race’
Jorde, L. B., & Wooding, S. P. (2004) · Nature Genetics
Race, Genetics, and SocietyForensic and Genetic Research
Cited by 637
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Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
Bamshad, M., Lin, R. C., Law, D. J., Watkins, W. S., Krakowiak, P. A., Moore, M. E., Franceschini, P., Lala, R., Holmes, L. B., Gebuhr, T. C., et al. (1997) · Nature Genetics
Congenital limb and hand anomaliesDevelopmental Biology and Gene Regulation
Cited by 540
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Global diversity, population stratification, and selection of human copy-number variation
Sudmant, P. H., Mallick, S., Nelson, B. J., Hormozdiari, F., Krumm, N., Huddleston, J., Coe, B. P., Baker, C., Nordenfelt, S., Bamshad, M., et al. (2015) · Science
Genomic variations and chromosomal abnormalitiesForensic and Genetic Research
Cited by 345
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A comprehensive map of mobile element insertion polymorphisms in humans
Stewart, C., Kural, D., Strömberg, M. P., Walker, J. A., Konkel, M. K., Stütz, A. M., Urban, A. E., Grubert, F., Lam, H. Y. K., Lee, W.-P., et al. (2011) · PLoS Genetics
Chromosomal and Genetic VariationsGenomic variations and chromosomal abnormalities
Cited by 307
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Microsatellites as EWS/FLI response elements in Ewing's sarcoma
Gangwal, K., Sankar, S., Hollenhorst, P. C., Kinsey, M., Haroldsen, S. C., Shah, A. A., Boucher, K. M., Watkins, W. S., Jorde, L. B., Graves, B. J., et al. (2008) · Proceedings of the National Academy of Sciences
Sarcoma Diagnosis and TreatmentGenomics and Chromatin Dynamics
Cited by 297
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The UCLA-University of Utah epidemiologic survey of autism: prevalence
RITVO, E. R., Freeman, B. J., Pingree, C., MASON-BROTHERS, A., Jorde, L. B., Jenson, W. R., McMahon, W. M., Petersen, P. B., Mo, A., & Ritvo, A. (1989) · American Journal of Psychiatry
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 273
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The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling
RITVO, E. R., Jorde, L. B., MASON-BROTHERS, A., Freeman, B. J., Pingree, C., Jones, M. B., McMahon, W. M., Petersen, P. B., Jenson, W. R., & Mo, A. (1989) · American Journal of Psychiatry
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 255
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Overlooked roles of DNA damage and maternal age in generating human germline mutations
Gao, Z., Moorjani, P., Sasani, T. A., Pedersen, B. S., Quinlan, A. R., Jorde, L. B., Amster, G., & Przeworski, M. (2019) · Proceedings of the National Academy of Sciences
Genomics and Rare DiseasesDNA Repair Mechanisms
Cited by 229
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Toll-like Receptor 3 and Geographic Atrophy in Age-Related Macular Degeneration
Yang, Z., Stratton, C., Francis, P. J., Kleinman, M. E., Tan, P. L., Gibbs, D., Tong, Z., Chen, H., Constantine, R., Yang, X., et al. (2008) · New England Journal of Medicine
Retinal Diseases and TreatmentsRetinal Development and Disorders
Cited by 222
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The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome
Bamshad, M., Le, T., Watkins, W. S., Dixon, M. E., Kramer, B. E., Roeder, A. D., Carey, J. C., Root, S., Schinzel, A., Van Maldergem, L., et al. (1999) · The American Journal of Human Genetics
Congenital limb and hand anomaliesdental development and anomalies
Cited by 175
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