Discerning the Ancestry of European Americans in Genetic Association Studies

Principal components analysis corrects for stratification in genome-wide association studies

Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., & Reich, D. (2006) · Nature Genetics · doi:10.1038/ng1847 · Cited by 10,248

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442

A haplotype map of the human genome

The International HapMap Consortium (2005) · Nature · doi:10.1038/nature04226 · Cited by 5,858

Population Structure and Eigenanalysis

Patterson, N., Price, A. L., & Reich, D. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020190 · Cited by 5,280

The History and Geography of Human Genes

Cavalli-Sforza, L. L., Menozzi, P., & Piazza, A. (2018) · Princeton University Press eBooks · doi:10.2307/j.ctv301gjp · Cited by 3,175

Genomic Control for Association Studies

Devlin, B., & Roeder, K. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00997.x · Cited by 3,162 · cited 1×

A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene

Duerr, R. H., Taylor, K. D., Brant, S. R., Rioux, J. D., Silverberg, M. S., Daly, M. J., Steinhart, A. H., Abraham, C., Regueiro, M., Griffiths, A., et al. (2006) · Science · doi:10.1126/science.1135245 · Cited by 3,039

A Map of Recent Positive Selection in the Human Genome

Voight, B. F., Kudaravalli, S., Wen, X., & Pritchard, J. K. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040072 · Cited by 2,925

Association mapping in structured populations.

Pritchard, J. K., Stephens, M., Rosenberg, N., & Donnelly, P. (2000) · American Journal of Human Genetics · doi:10.1086/302959 · Cited by 2,066

The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

Altshuler, D., Hirschhorn, J. N., Klannemark, M., Lindgren, C. M., Vohl, M.-C., Nemesh, J., Lane, C. R., Schaffner, S. F., Bolk, S., Brewer, C., et al. (2000) · Nature Genetics · doi:10.1038/79216 · Cited by 1,766

Problems with a Causal Interpretation of Polygenic Score Differences between Jewish and non-Jewish Respondents in the Wisconsin Longitudinal StudyPreprint

Jeremy Freese, A., Domingue, B. W., Trejo, S., Sicinski, K., & Herd, P. (2019) · doi:10.31235/osf.io/eh9tq · Cited by 15

Genetic variants associated with susceptibility of Ashkenazi Jews to West Nile virus infection

Danial‐Farran, N., Eghbaria, S., Schwartz, N., Kra-Oz, Z., & Bisharat, N. (2014) · Epidemiology and Infection · doi:10.1017/s0950268814001290 · Cited by 14

PTPN22 C1858T and the risk of psoriasis: a meta-analysis

Chen, Y.-F., & Chang, J. S.-M. (2012) · Molecular Biology Reports · doi:10.1007/s11033-012-1630-z · Cited by 14

Magnitude of Stratification in Human Populations and Impacts on Genome Wide Association Studies

Hao, K., Chudin, E., Greenawalt, D. M., & Schadt, E. E. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008695 · Cited by 15

Psoriasis risk SNPs and their association with HIV-1 control

Nititham, J., Gupta, R., Zeng, X., Hartogensis, W., Nixon, D. F., Deeks, S. G., Hecht, F. M., & Liao, W. J. (2016) · Human Immunology · doi:10.1016/j.humimm.2016.10.018 · Cited by 14

Converging Evidence for the Nogo-66 Receptor Gene in Schizophrenia

Voineskos, A. N. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0477-09.2009 · Cited by 14

Commonalities in the genetics of Alzheimer’s disease and Parkinson’s disease

Grünblatt, E. (2008) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.8.12.1865 · Cited by 14

Genetic architecture of prostate cancer in the Ashkenazi Jewish population

Vijai, J., Kirchhoff, T., Gallagher, D. J., Hamel, N., Guha, S., Darvasi, A., Lencz, T., Foulkes, W. D., Offit, K., & Klein, R. J. (2011) · British Journal of Cancer · doi:10.1038/bjc.2011.307 · Cited by 13

Genes, Environments, and Developmental Research: Methods for a Multi-Site Study of Early Substance Abuse

Costello, E. J., Eaves, L. J., Sullivan, P. F., Kennedy, M. A., Conway, K. P., Adkins, D. E., Angold, A. C., Clark, S. L., Erkanli, A., McClay, J. L., et al. (2013) · Twin Research and Human Genetics · doi:10.1017/thg.2013.6 · Cited by 13

Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control

Rosa, A., Abrantes, P., Sousa, I., Francisco, V., Santos, P., Francisco, D., Xavier, J. M., & Oliveira, S. A. (2016) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000694 · Cited by 13

Gene–environment interaction: Oxytocin receptor (OXTR) polymorphisms and parenting style as potential predictors for depressive symptoms

Keijser, R., Åslund, C., Nilsson, K. W., & Olofsdotter, S. (2021) · Psychiatry Research · doi:10.1016/j.psychres.2021.114057 · Cited by 13

Geographic Ancestry and Mortality from Ischemic Heart Disease: Evidence from the Finnish Population Register

Saarela, J. M., & Finnäs, F. (2009) · Population review · doi:10.1353/prv.0.0015 · Cited by 13

Modeling geographic risk of complex congenital heart defects in Eastern Wisconsin.

Cronk, C., Gangnon, R., Cossette, S., McElroy, J., & Pelech, A. (2011) · Birth defects research. Clinical and molecular teratology · doi:10.1002/bdra.20828 · Cited by 14

Genotypically determined ancestry across an infertile population: ovarian reserve and response parameters are not influenced by continental origin

Olcha, M., Franasiak, J. M., Shastri, S. M., Molinaro, T. A., Congdon, H., Treff, N. R., & Scott, R. T. (2016) · Fertility and Sterility · doi:10.1016/j.fertnstert.2016.03.052 · Cited by 13

Mathematical Approaches to Polymer Sequence Analysis and Related Problems

Catanzaro, D. (2010) · Springer eBooks · doi:10.1007/978-1-4419-6800-5 · Cited by 12

An integrated analysis of the association between Ts gene polymorphisms and clinical outcome in gastric and colorectal cancer patients treated with 5-FU-based regimens

Wang, Y., Xue, H., Wang, Z., & Fang, J. (2013) · Molecular Biology Reports · doi:10.1007/s11033-013-2557-8 · Cited by 12

Genetic contribution to multiple sclerosis risk among Ashkenazi Jews

Khankhanian, P., Matsushita, T., Madireddy, L., Lizée, A., Din, L., Moré, J. M., Gourraud, P., Hauser, S. L., Baranzini, S. E., & Oksenberg, J. R. (2015) · BMC Medical Genetics · doi:10.1186/s12881-015-0201-2 · Cited by 12

Arabidopsis lyrata Genetics

Savolainen, O., & Kuittinen, H. (2010) · Springer eBooks · doi:10.1007/978-1-4419-7118-0_12 · Cited by 12

Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis method

Peloso, G. M., Timofeev, N., & Lunetta, K. L. (2009) · BMC Proceedings · doi:10.1186/1753-6561-3-s7-s108 · Cited by 12

Fast principal components analysis reveals convergent evolution of ADH1B gene in Europe and East AsiaPreprint

Galinsky, K. J., Bhatia, G., Loh, P., Georgiev, S., Mukherjee, S., Patterson, N. J., & Price, A. L. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/018143 · Cited by 13

Common variations within HACE1 gene and neuroblastoma susceptibility in a Southern Chinese population

Zhang, Z., Zhang, R., Zhu, J., Wang, F., Yang, T., Zou, Y., He, J., & Xia, H. (2017) · OncoTargets and Therapy · doi:10.2147/ott.s129042 · Cited by 11

Mapping the genetic diversity of HLA haplotypes in the Japanese populations

Saw, W., Liu, X., Khor, C. C., Takeuchi, F., Katsuya, T., Kimura, R., Nabika, T., Ohkubo, T., Tabara, Y., Yamamoto, K., et al. (2015) · Scientific Reports · doi:10.1038/srep17855 · Cited by 11

Integrative analysis of single nucleotide polymorphisms and gene expression efficiently distinguishes samples from closely related ethnic populations

Yang, H., Wang, P., Lin, C., Chen, C.-H., & Chen, C. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-346 · Cited by 11

Genotype-Based Ancestral Background Consistently Predicts Efficacy and Side Effects across Treatments in CATIE and STAR*D

Adkins, D. E., de Souza, R. P., Åberg, K. A., Clark, S. L., McClay, J. L., Sullivan, P. F., & van den Oord, E. J. C. G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055239 · Cited by 10

Assortative Mating by Ethnicity in Longevous Families

Sebastiani, P., Gurinovich, A., Bae, H. T., Andersen, S. L., & Perls, T. T. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00186 · Cited by 11

Genetic legacy of state centralization in the Kuba Kingdom of the Democratic Republic of the Congo

van Dorp, L., Lowes, S., Weigel, J., Ansari‐Pour, N., López, S., Mendoza‐Revilla, J., Robinson, J. A., Henrich, J., Thomas, M., Nunn, N., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1811211115 · Cited by 10

A Small Number of Candidate Gene SNPs Reveal Continental Ancestry in African Americans

Kodaman, N., Aldrich, M. C., Smith, J. R., Signorello, L. B., Bradley, K., Breyer, J. P., Cohen, S. S., Long, J., Cai, Q., Giles, J., et al. (2012) · Annals of Human Genetics · doi:10.1111/j.1469-1809.2012.00738.x · Cited by 10

Impact of Population Substructure on Trend Tests for Genetic Case–Control Association Studies

Zheng, G., Li, Z., Gail, M. H., & Gastwirth, J. L. (2009) · Biometrics · doi:10.1111/j.1541-0420.2009.01264.x · Cited by 10

Multiple correspondence discriminant analysis: An application to detect stratification in copy number variation

Cáceres, A., Basagaña, X., & González, J. R. (2010) · Statistics in Medicine · doi:10.1002/sim.3890 · Cited by 10

Sexually dimorphic DNA methylation and gene expression patterns in human first trimester placenta

Gonzalez, T. L., Willson, B. E., Wang, E. T., Taylor, K. D., Novoa, A., Swarna, A., Ortiz, J. C., Zeno, G. J., Jefferies, C. A., Lawrenson, K., et al. (2024) · Biology of Sex Differences · doi:10.1186/s13293-024-00629-9 · Cited by 9

A comparison of DMET Plus microarray and genome-wide technologies by assessing population substructure

Jackson, J. N., Long, K. M., He, Y., Motsinger‐Reif, A. A., McLeod, H. L., & Jack, J. (2016) · Pharmacogenetics and Genomics · doi:10.1097/fpc.0000000000000200 · Cited by 9

Let’s Not Repeat History’s Mistakes: Two Cautions to Scientists on the Use of Race in Alzheimer’s Disease and Alzheimer’s Disease Related Dementias Research

Stites, S. D., & Coe, N. B. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-220507 · Cited by 10

Fine mapping of the myosin light chain kinase (MYLK) gene replicates the association with asthma in populations of Spanish descent

Acosta‐Herrera, M., Pino-Yanes, M. D. M., Ma, S., Barreto-Luis, A., Corrales, A., Cumplido, J., Perez-Rodriguez, E., Campo, P., Eng, C. S., García-Robaina, J. C., et al. (2015) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2015.04.025 · Cited by 9

Discrimination between human populations using a small number of differentially methylated CpG sites: a preliminary study using lymphoblastoid cell lines and peripheral blood samples of European and Chinese origin

Daca‐Roszak, P., Jaksik, R., Paczkowska, J., Witt, M., & Ziętkiewicz, E. (2020) · BMC Genomics · doi:10.1186/s12864-020-07092-x · Cited by 9

Relationship between polycystic ovary syndrome and ancestry in European Americans

Bjonnes, A., Saxena, R., & Welt, C. K. (2016) · Fertility and Sterility · doi:10.1016/j.fertnstert.2016.08.033 · Cited by 9

Genetic associations with longevity are on average stronger in females than in males

Zeng, Y., Chen, H., Liu, X., Song, Z., Yao, Y., Lei, X., Lv, X., Cheng, L., Chen, Z., Bai, C., et al. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e23691 · Cited by 8

Empirical prediction of genomic susceptibilities for multiple cancer classes

Kim, M., & Kim, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1318383110 · Cited by 9

A globally occurring indel polymorphism in the promoter of the IFNA2 gene is not associated with severity of malaria but with the positivity rate of HCV

Tena‐Tomás, C., Messias-Reason, I., Le, S. H., Tomiuk, J., Kemsner, P. G., & Kun, J. F. J. (2008) · BMC Genetics · doi:10.1186/1471-2156-9-80 · Cited by 8

Genetics and Genomic Basis of Sleep Disorders in Humans

Pack, A. I., Keenan, B. T., Byrne, E. M., & Gehrman, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-24288-2.00031-3 · Cited by 8

The Inflammatory Gene Pathway Is Not a Major Contributor to Polycystic Ovary Snydrome

Bhatt, S., Mutharasan, P., Garcia, O. A., Jafari, N., Legro, R. S., Dunaif, A. E., & Urbanek, M. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2013-2342 · Cited by 8

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European population

Lu, T. T., Lao, Ó., Nothnagel, M., Junge, O., Freitag‐Wolf, S., Caliebe, A., Balaščaková, M., Bertranpetit, J., Bindoff, L. A., Comas, D., et al. (2009) · European Journal of Human Genetics · doi:10.1038/ejhg.2008.266 · Cited by 8

Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes

Kumasaka, N., Yamaguchi‐Kabata, Y., Takahashi, A., Kubo, M., Nakamura, Y., & Kamatani, N. (2010) · Journal of Human Genetics · doi:10.1038/jhg.2010.63 · Cited by 8

An assessment of the portability of ancestry informative markers between human populations

Myles, S., Stoneking, M., & Timpson, N. J. (2009) · BMC Medical Genomics · doi:10.1186/1755-8794-2-45 · Cited by 8

Ancestral Informative Marker Selection and Population Structure Visualization Using Sparse Laplacian Eigenfunctions

Zhang, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013734 · Cited by 8

Human ancestry indentification under resource constraints -- what can one chromosome tell us about human biogeographical ancestry?

Toma, T. T., Dawson, J. M., & Adjeroh, D. (2018) · BMC Medical Genomics · doi:10.1186/s12920-018-0412-4 · Cited by 7

Replication of recently identified associated single-nucleotide polymorphisms from six autoimmune diseases in Genetic Analysis Workshop 16 rheumatoid arthritis data

Deshmukh, H., Kim-Howard, X., & Nath, S. K. (2009) · BMC Proceedings · doi:10.1186/1753-6561-3-s7-s31 · Cited by 7

A functional variant in the coding region of CAMTA2 is associated with left ventricular hypertrophy by affecting the activation of Nkx2.5-dependent transcription

Song, W., Lin, Y.-H., Sun, K., Zhang, Y., Song, Y., Hou, L., Zhang, C., Hui, R., & Chen, J. (2016) · Journal of Hypertension · doi:10.1097/hjh.0000000000000873 · Cited by 7

High-resolution inference of genetic relationships among Jewish populations

Kopelman, N. M., Stone, L., Hernandez, D. G., Gefel, D., Singleton, A., Heyer, É., Feldman, M. W., Hillel, J., & Rosenberg, N. A. (2020) · European Journal of Human Genetics · doi:10.1038/s41431-019-0542-y · Cited by 6

Efficient Population Assignment and Outlier Detection in Human Populations Using Biallelic Markers Chosen by Principal Component–Based Rankings

Raaum, R. L., Wang, A. B., Al‐Meeri, A., & Mulligan, C. J. (2010) · BioTechniques · doi:10.2144/000113426 · Cited by 6

Shared polymorphisms and modifiable behavior factors for myocardial infarction and high cholesterol in a retrospective population study

Liang, Y., & Kelemen, A. (2017) · Medicine · doi:10.1097/md.0000000000007683 · Cited by 6

Asymptotic powers for matched trend tests and robust matched trend tests in case-control genetic association studies

Zang, Y., Fung, W. K., & Zheng, G. (2009) · Computational Statistics & Data Analysis · doi:10.1016/j.csda.2009.07.011 · Cited by 6

Application of highly differentiated SNPs between Japanese Black and Holstein to a breed assignment test between Japanese Black and F1 (Japanese Black x Holstein) and Holstein

Nishimura, S., Watanabe, T., Ogino, A., Shimizu, K., MORITA, M., Sugimoto, Y., & Takasuga, A. (2012) · Animal Science Journal · doi:10.1111/j.1740-0929.2012.01036.x · Cited by 6

Genetic history of the population of Crete

Petros Drineas, B., Tsetsos, F., Plantinga, A., Lazaridis, I., Yannaki, E., Razou, A., Kanaki, K., Michalodimitrakis, M., Pérez‐Jiménez, F., Silvestro, G. D., et al. (2019) · Annals of Human Genetics · doi:10.1111/ahg.12328 · Cited by 11

Transcriptome variation in human populations and its potential application in forensics

Daca‐Roszak, P., & Ziętkiewicz, E. (2019) · Journal of Applied Genetics · doi:10.1007/s13353-019-00510-1 · Cited by 7

Evaluation of self-reported ethnicity in a case-control population: the stroke prevention in young women study

Mez, J. B., Cole, J. W., Howard, T. D., MacClellan, L. R., Stine, O. C., O’Connell, J. R., Wozniak, M. A., Stern, B. J., Sorkin, J. D., Mitchell, B. D., et al. (2009) · BMC Research Notes · doi:10.1186/1756-0500-2-260 · Cited by 5

The Brachial and Crural Indices of Modern North American Populations

Garcia, R. V. (2015) · Cited by 5

The Identification of Colon Cancer Susceptibility Genes by Using Genome-Wide Scans

Daley, D. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-759-4_1 · Cited by 5

High mammographic density in women of Ashkenazi Jewish descent

Caswell-Jin, J. L., Kerlikowske, K. M., Shepherd, J., Cummings, S. R., Hu, D., Huntsman, S., & Ziv, E. (2013) · Breast Cancer Research · doi:10.1186/bcr3424 · Cited by 4

Biology, Immigration, and Public Policy

Christainsen, G. B. (2012) · Kyklos · doi:10.1111/j.1467-6435.2012.00532.x · Cited by 5

Genome-wide methylation data mirror ancestry informationPreprint

Rahmani, E., Shenhav, L., Schweiger, R., Yousefi, P., Huen, K., Eskenazi, B., Eng, C. S., Huntsman, S., Hu, D., Galanter, J., et al. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/066340 · Cited by 5

A comprehensive analysis of clinical and polygenic germline influences on somatic mutational burden

Taraszka, K., Groha, S., King, D., Tell, R. W., White, K. P., Ziv, E., Zaitlen, N., & Gusev, A. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2023.12.010 · Cited by 4

Variations in Genetic Diversity of Invasive Species Lithobates catesbeianus in China

Zhang, J., Xu, C., Wang, S., Wang, S., & Li, Y. (2024) · Animals · doi:10.3390/ani14091287 · Cited by 4

Genetics and Genomics of Human Population Structure

Ramachandran, S., Tang, H., Gutenkunst, R. N., & Bustamante, C. D. (2009) · Springer eBooks · doi:10.1007/978-3-540-37654-5_22 · Cited by 4

European American Stratification in Ovarian Cancer Case Control Data: The Utility of Genome-Wide Data for Inferring Ancestry

Raska, P., Iversen, E. S., Chen, A., Chen, Z., Fridley, B. L., Permuth‐Wey, J., Tsai, Y.-Y., Vierkant, R. A., Goode, E. L., Risch, H. A., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035235 · Cited by 4

Ecogeographic patterns in fetal limb proportions

Waxenbaum, E. B., Warren, M. W., Holliday, T. W., Byrd, J. E., & Cole, T. M. (2019) · American Journal of Physical Anthropology · doi:10.1002/ajpa.23814 · Cited by 4

Correction: Genetic Structure of Europeans: A View from the North–East

Nelis, M., Esko, T., Mägi, R., Zimprich, F., Zimprich, A. A., Toncheva, D. I., Karachanak-Yankova, S., Piskackova, T., Balaščák, I., Peltonen, L., et al. (2010) · PLoS ONE · doi:10.1371/annotation/2849e182-aef5-4e2b-a5ac-0b74b30e5f48 · Cited by 5

hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets

Johnson, T. A., Niimura, Y., Tanaka, H., Nakamura, Y., & Tsunoda, T. (2011) · Genome biology · doi:10.1186/gb-2011-12-3-r21 · Cited by 3

POPSTR: Inference of Admixed Population Structure Based on Single-Nucleotide Polymorphisms and Copy Number Variations

Ahn, J., Conkright, B., Boca, S. M., & Madhavan, S. (2018) · Journal of Computational Biology · doi:10.1089/cmb.2017.0127 · Cited by 3

Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts

Anwar, M. Y., Graff, M., Highland, H. M., Smit, R. A. J., Wang, Z., Buchanan, V. L., Young, K. L., Kenny, E. E., Fernández‐Rhodes, L., Liu, S., et al. (2023) · Human Genetics · doi:10.1007/s00439-023-02593-7 · Cited by 2

Genomic Landscape of Breast Cancer: Study Across Diverse Ethnic Groups

Garibaldi-Ríos, A. F., Figuera, L. E., Zúñiga‐González, G. M., Gómez‐Meda, B. C., Puebla‐Pérez, A. M., Rivera-Cameras, A., Magaña‐Torres, M. T., García‐Ortíz, J. E., Dávalos‐Rodríguez, I. P., Reynoso, M. A. R., et al. (2025) · Diseases · doi:10.3390/diseases13030086 · Cited by 3

No association between genetic ancestry and susceptibility to asthma or atopy in Canary Islanders

Pino-Yanes, M. D. M., Corrales, A., Cumplido, J., González‐Pérez, R., Torres-Galván, M. J., Fernández, O. A., Sánchez‐Machín, I., Figueroa, J., Sánchez-Palacios, A., Villar, J., et al. (2012) · Immunogenetics · doi:10.1007/s00251-012-0631-3 · Cited by 2

Using Genomic Data to Find Disease-Modifying Loci in Huntington’s Disease (HD)

Holmans, P., & Stone, T. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7825-0_20 · Cited by 2

HUMAN GENETIC VARIATION IN THE BALTIC SEA REGION: FEATURES OF POPULATION HISTORY AND NATURAL SELECTION

Lappalainen, T. (2009) · Työväentutkimus Vuosikirja · Cited by 2

Exploring Human Evolutionary History and Biological Nature

Vincenzo, F. D., Macciardi, F. M., & Manzi, G. (2024) · Springer eBooks · doi:10.1007/978-3-031-61187-2_4 · Cited by 1

Confirmation of a founder effect in a Northern European population of a new β-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))

Marchi, N., Pissard, S., Cliquennois, M., Vasseur, C., Metayer, N. L., Méreau, C., Jouet, J. P., Georgel, A., Génin, E., & Rosé, C. (2014) · European Journal of Human Genetics · doi:10.1038/ejhg.2014.263 · Cited by 1

Identifying susceptibility genes of IgA nephropathy: research in progress

Barua, M., & Pei, Y. (2009) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfp376 · Cited by 1

Document Title: Population Genetics of SNPs for Forensic Purposes (Updated)

Kídd, K. K. (2008) · Cited by 1

Report Correlation between Genetic and Geographic Structure in Europe

Lao, Ó., Lu, T. T., Nothnagel, M., Junge, O., Freitag‐Wolf, S., Caliebe, A., Balaščaková, M., Bertranpetit, J., Bindoff, L. A., Comas, D., et al. (2008) · Cited by 1

Genome-wide versus transcriptome-wide association studies: Prospects and limitations

Mohammed, J. (2024) · Ecological Genetics and Genomics · doi:10.1016/j.egg.2024.100221 · Cited by 1

Polimorfismos de los genes JAG1, MEF2C y BDNF asociados con la densidad mineral ósea en mujeres del norte de México

González-Peña, S. M., Campos‐Góngora, E., Ávila-Rodríguez, H. G., Ramírez‐López, E., Velázquez‐Cruz, R., & Jiménez‐Salas, Z. (2018) · Biomédica · doi:10.7705/biomedica.v38i3.4014 · Cited by 1

Research highlights

(2008) · Nature Genetics · doi:10.1038/ng0308-273 · Cited by 1

Associação de etnia auto referida e ancestralidade genética com fatores de risco de doença cardiovascular em uma amostra populacional brasileira: ELSA - Brasil

Santos, H. C. (2015) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.5.2015.tde-04082015-094037 · Cited by 1

Concepts of Population Genomics

Weale, M. E., & Goldstein, D. B. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-369420-1.00002-0 · Cited by 1

Investigation of Candidate Genes and HLA-Related Risk Factors in a Genetic Study of Autoimmune Disease

Bronson, P. G. (2010) · eScholarship (California Digital Library) · Cited by 1

k2v: A Containerized Workflow for Creating VCF Files from Kintelligence Targeted Sequencing DataPreprint

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