Hammer, Michael F.

A high-coverage genome sequence from an archaic denisovan individual

Meyer, M., Kircher, M., Gansauge, M.-T., Li, H., Racimo, F., Mallick, S., Schraiber, J. G., Jay, F., Prüfer, K., de Filippo, C., et al. (2012) · Science

Pleistocene-Era Hominins and ArchaeologyForensic and Genetic Research

Cited by 1,967

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

Ancient human genomes suggest three ancestral populations for present-day Europeans

Lazaridis, I., Patterson, N., Mittnik, A., Renaud, G., Mallick, S., Kirsanow, K., Sudmant, P. H., Schraiber, J. G., Castellano, S., Lipson, M., et al. (2014) · Nature

Forensic and Genetic ResearchGenetic diversity and population structure

Cited by 1,357

Genome-wide patterns of population structure and admixture among Hispanic/Latino populations

Bryc, K., Velez, C., Karafet, T., Moreno-Estrada, A., Reynolds, A., Auton, A., Hammer, M., Bustamante, C. D., & Ostrer, H. (2010) · Proceedings of the National Academy of Sciences

Forensic and Genetic ResearchGenetic diversity and population structure

Cited by 442

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP

Veeramah, K. R., O'Brien, J. E., Meisler, M. H., Cheng, X., Dib-Hajj, S. D., Waxman, S. G., Talwar, D., Girirajan, S., Eichler, E. E., Restifo, L. L., et al. (2012) · The American Journal of Human Genetics

Epilepsy research and treatmentIon channel regulation and function

Cited by 438

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

Higher Levels of Neanderthal Ancestry in East Asians than in Europeans

Wall, J. D., Yang, M. A., Jay, F., Kim, S. K., Durand, E. Y., Stevison, L. S., Gignoux, C., Woerner, A., Hammer, M. F., & Slatkin, M. (2013) · Genetics

Pleistocene-Era Hominins and ArchaeologyForensic and Genetic Research

Cited by 249

Complex Patterns of Admixture across the Indonesian Archipelago

Hudjashov, G., Karafet, T. M., Lawson, D. J., Downey, S., Savina, O., Sudoyo, H., Lansing, J. S., Hammer, M. F., & Cox, M. P. (2017) · Molecular Biology and Evolution

Forensic and Genetic ResearchGenetic diversity and population structure

Cited by 191

A haplotype at STAT2 introgressed from neanderthals and serves as a candidate of positive selection in Papua New Guinea

Mendez, F. L., Watkins, J. C., & Hammer, M. F. (2012) · The American Journal of Human Genetics

Pleistocene-Era Hominins and ArchaeologyForensic and Genetic Research

Cited by 156

Model-based analyses of whole-genome data reveal a complex evolutionary history involving archaic introgression in Central African Pygmies

Hsieh, P., Woerner, A. E., Wall, J. D., Lachance, J., Tishkoff, S. A., Gutenkunst, R. N., & Hammer, M. F. (2016) · Genome Research

Pleistocene-Era Hominins and ArchaeologyForensic and Genetic Research

Cited by 105

Global genetic variation at OAS1 provides evidence of archaic admixture in Melanesian populations

Mendez, F. L., Watkins, J. C., & Hammer, M. F. (2012) · Molecular Biology and Evolution

Forensic and Genetic ResearchPleistocene-Era Hominins and Archaeology

Cited by 79

Increased Resolution of Y Chromosome Haplogroup T Defines Relationships among Populations of the Near East, Europe, and Africa

Mendez, F. L., Karafet, T. M., Krahn, T., Ostrer, H., Soodyall, H., & Hammer, M. F. (2011) · Human Biology

Forensic and Genetic ResearchGenetic diversity and population structure

Cited by 60

Eye movement defects in KO zebrafish reveals SRPK3 as a causative gene for an X‐linked intellectual disability

Kim, C.-H., Lee, Y.-R., Thomas, M., Roychaudhury, A., Skinner, C., Maconachie, G., Crosier, M., Horak, H., Constantinescu, C., Choi, T.-I., et al. (2023) · Research Square

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 3