Goldstein, David B.

Inferring genetic ancestry: Opportunities, challenges, and implications

Royal, C. D., Novembre, J., Fullerton, S. M., Goldstein, D. B., Long, J. C., Bamshad, M. J., & Clark, A. G. (2010) · The American Journal of Human Genetics

Forensic and Genetic ResearchRace, Genetics, and Society

Cited by 271

Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine

Petrovski, S., & Goldstein, D. B. (2016) · Genome Biology

Genomics and Rare DiseasesRace, Genetics, and Society

Cited by 255

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

Dobbs, K., Domínguez Conde, C., Zhang, S.-Y., Parolini, S., Audry, M., Chou, J., Haapaniemi, E., Keles, S., Bilic, I., Okada, S., et al. (2015) · New England Journal of Medicine

Immunodeficiency and Autoimmune DisordersBlood disorders and treatments

Cited by 201

Geographical genomics of human leukocyte gene expression variation in southern Morocco

Idaghdour, Y., Czika, W., Shianna, K. V., Lee, S. H., Visscher, P. M., Martin, H. C., Miclaus, K., Jadallah, S. J., Goldstein, D. B., Wolfinger, R. D., et al. (2010) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 151

Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease

Raghavan, N. S., Brickman, A. M., Andrews, H., Manly, J. J., Schupf, N., Lantigua, R., Wolock, C. J., Kamalakaran, S., Petrovski, S., Tosto, G., et al. (2018) · Annals of Clinical and Translational Neurology

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 141

A predominantly indigenous paternal heritage for the Austronesian-speaking peoples of insular Southeast Asia and Oceania

Capelli, C., Wilson, J. F., Richards, M., Stumpf, M. P. H., Gratrix, F., Oppenheimer, S., Underhill, P., Pascali, V. L., Ko, T.-M., & Goldstein, D. B. (2001) · The American Journal of Human Genetics

Forensic and Genetic ResearchPacific and Southeast Asian Studies

Cited by 136

One gene, many neuropsychiatric disorders: lessons from Mendelian diseases

Zhu, X., Need, A. C., Petrovski, S., & Goldstein, D. B. (2014) · Nature Neuroscience

Genetic Associations and EpidemiologyGenetics and Neurodevelopmental Disorders

Cited by 131

Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures

Petrovski, S., Küry, S., Myers, C. T., Anyane-Yeboa, K., Cogné, B., Bialer, M., Xia, F., Hemati, P., Riviello, J., Mehaffey, M., et al. (2016) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 114

Common genetic variation and performance on standardized cognitive tests

Cirulli, E. T., Kasperavičiūtė, D., Attix, D. K., Need, A. C., Ge, D., Gibson, G., & Goldstein, D. B. (2010) · European Journal of Human Genetics

Genetic Associations and EpidemiologyCognitive Abilities and Testing

Cited by 98

A Genome-wide Comparison of the Functional Properties of Rare and Common Genetic Variants in Humans

Zhu, Q., Ge, D., Maia, J. M., Zhu, M., Petrovski, S., Dickson, S. P., Heinzen, E. L., Shianna, K. V., & Goldstein, D. B. (2011) · The American Journal of Human Genetics

Evolution and Genetic DynamicsGenetic Associations and Epidemiology

Cited by 96

TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability

Heimer, G., Oz-Levi, D., Eyal, E., Edvardson, S., Nissenkorn, A., Ruzzo, E. K., Szeinberg, A., Maayan, C., Mai-Zahav, M., Efrati, O., et al. (2016) · European Journal of Paediatric Neurology

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 49

Estimating the age of mutations using variation at linked markers

Reich, D. E., & Goldstein, D. B. (1999) · Microsatellites: Evolution and Applications

Genetic Associations and EpidemiologyForensic and Genetic Research

Cited by 29

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases

Mitchell, J., Camacho, N., Shea, P., Stopsack, K. H., Joseph, V., Burren, O. S., Dhindsa, R. S., Nag, A., Berchuck, J. E., O’Neill, A., et al. (2025) · Nature Communications

BRCA gene mutations in cancerProstate Cancer Treatment and Research

Cited by 19