Results 101 to 110 of about 2,061 (188)

Inbreeding and deleterious variation in South Asian populations. [PDF]

Sci Rep
Wall JD, Rodrigues MF.
europepmc   +1 more source

Population-Specific Mutational Spectrum of Autosomal Recessive Nonsyndromic Hearing Loss in Croatian Roma: Implications for Clinical Genetics. [PDF]

Genes (Basel)
Kutija Fučkar I, Zajc Petranović M, Martinović Klarić I, Peričić Salihović M, Barać Lauc L.   +4 more
europepmc   +1 more source

Family-based community organization in Neolithic Northern China from 8,800 to 7,500 years ago. [PDF]

Innovation (Camb)
Liu T, Zhao Z, Guo M, Cao P, Zhuang L, Zhang W, Liu F, Shi H, Song M, Zhao M, Ju D, Miao B, Fu Q.   +12 more
europepmc   +1 more source

Uncovering a Medieval Pogrom: Genetic History of a Jewish Community in Catalonia (Spain). [PDF]

Genes (Basel)
Pallarés-Viña L, Cuesta-Aguirre DR, Campoy-Caballero MR, Armentano N, Colet A, Malgosa A, Santos C.   +6 more
europepmc   +1 more source

Human genetic diversity across South Asian populations: A systematic review and meta-analysis. [PDF]

Medicine (Baltimore)
Rehman SU, Abbas GH, Abbas GH.
europepmc   +1 more source

The genetic footprint of the European Roma diaspora: evidence from the Balkans to the Iberian Peninsula. [PDF]

Hum Genet
Ena GF, Giménez A, Carballo-Mesa A, Lišková P, Lišková P, Araújo Castro E Silva M, Comas D.   +6 more
europepmc   +1 more source

A rapid accurate approach to inferring pedigrees in endogamous populations. [PDF]

Genetics
Williams CM, Scelza BA, Slack SD, Font-Porterias N, Al-Hindi DR, Mathias RA, Watson H, Barnes KC, Lange E, Johnson RK, Gignoux CR, Ramachandran S, Henn BM.   +12 more
europepmc   +1 more source

Uncovering the Genetic Structure of the Sekler Population in Transylvania Through Genome-Wide Autosomal Data. [PDF]

Genes (Basel)
Szabó A, Bánfai Z, Sümegi K, Ádám V, Gallyas F, Kásler M, Melegh B.   +6 more
europepmc   +1 more source

Is he really my relative? Kinship cases in substructured populations: a study on the Lebanese population. [PDF]

Forensic Sci Res
El Andari A, Mansour I.
europepmc   +1 more source

A Novel Bi-Allelic Mutation in the Paired Box 7 Gene Causing Congenital Myopathy 19 in an Indian Family. [PDF]

Ann Indian Acad Neurol
Saluja A, Sahib A, Haque A, Yadav V.
europepmc   +1 more source