DNA Sequence Variation in a 3.7-kb Noncoding Sequence 5′ of the CYP1A2 Gene: Implications for Human Population History and Natural Selection

द्वारा Wooding, S. P., Watkins, W. S., Bamshad, M. J., Dunn, D. M., Weiss, R. B., Jorde, L. B.
प्रकाशित 2002

The Distribution of Human Genetic Diversity: A Comparison of Mitochondrial, Autosomal, and Y-Chromosome Data

द्वारा Jorde, L. B., Watkins, W. S., Bamshad, M. J., Dixon, M. E., Ricker, C. E., Seielstad, M. T., Batzer, M. A.
प्रकाशित 2000

Patterns of Ancestral Human Diversity: An Analysis of Alu-Insertion and Restriction-Site Polymorphisms

द्वारा Watkins, W. S., Ricker, C. E., Bamshad, M. J., Carroll, M. L., Nguyen, S. V., Batzer, M. A., Harpending, H. C., Rogers, A. R., Jorde, L. B.
प्रकाशित 2001

Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic data.

द्वारा Jorde, L B, Bamshad, M J, Watkins, W S, Zenger, R, Fraley, A E, Krakowiak, P A, Carpenter, K D, Soodyall, H, Jenkins, T, Rogers, A R
प्रकाशित 1995

A Homozygous Missense Mutation in SLC25A16 is Associated with Autosomal Recessive Isolated Fingernail Dysplasia in a Pakistani Family

द्वारा Khan, S., Ansar, M., Khan, A. Kamal, Shah, K., Muhammad, N., Shahzad, S., Nickerson, D.A., Bamshad, M.J., Santos-Cortez, R.L.P., Leal, S.M., Ahmad, W.
में प्रकाशित Br J Dermatol (2017)

A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families

द्वारा Ahmad, F., Ansar, M., Mehmood, S., Izoduwa, A., Lee, K., Nasir, A., Abrar, M., Mehmood, S., Ullah, A., Aziz, A., Smith, J.D., Shendure, J., Bamshad, M.J., Nicekrson, D.A., Santos-Cortez, R.L.P., Leal, S.M., Ahmad, W.
में प्रकाशित J Eur Acad Dermatol Venereol (2015)

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.

द्वारा Tavormina, P L, Bellus, G A, Webster, M K, Bamshad, M J, Fraley, A E, McIntosh, I, Szabo, J, Jiang, W, Jabs, E W, Wilcox, W R, Wasmuth, J J, Donoghue, D J, Thompson, L M, Francomano, C A
प्रकाशित 1999