Results 151 to 160 of about 12,390 (239)

The OurHealth Study: A digital genomic cohort for cardiometabolic risk mechanisms in US South Asians. [PDF]

NPJ Digit Med
Ganesh S, Bhattacharya R, Bhatnagar A, Madnani R, Russo C, Haidermota S, Oruganty B, Bhavsar H, Shah P, Pitafi S, Uppal N, Sengupta N, Rice K, Conomos MP, Dave R, Khandelwal A, Patel AP, Paruchuri K, Levitsky Y, Parulkar SS, Khera R, Gulati M, Khera AV, Hornsby WE, Palaniappan L, Natarajan P.   +25 more
europepmc   +1 more source

The rate of identical-by-descent segment sharing between close and distant relatives. [PDF]

HGG Adv
Williams AL.
europepmc   +1 more source

Expansion of genotypic and phenotypic findings in ADAMTS18-related ocular pathology. [PDF]

Am J Ophthalmol Case Rep
August AH, Procopio RA, Rapuano CJ, Pulido JS.   +3 more
europepmc   +1 more source

Implications of endogamy in the southwest Eurasian highlands: another look at Jack Goody’s theory of production, property and kinship

, 2020
Heady, P., Yalçın-Heckmann, L.
core   +1 more source

Distinct positions of genetic and oral histories: Perspectives from India. [PDF]

HGG Adv
Biddanda A, Bandyopadhyay E, de la Fuente Castro C, Witonsky D, Urban Aragon JA, Pasupuleti N, Moots HM, Fonseca R, Freilich S, Stanisavic J, Willis T, Menon A, Mustak MS, Kodira CD, Naren AP, Sikdar M, Rai N, Raghavan M.   +17 more
europepmc   +1 more source

A founder heterozygous mutation in methyl-CpG binding domain protein 4 (MBD4) prevalent among Israeli Christian Arabs predisposes to increased mutagenesis. [PDF]

Haematologica
Dadi G, Rosen S, Naor H, Hellou E, Chapal-Ilani N, Bacharach T, Kaushansky N, Shlush LL.   +7 more
europepmc   +1 more source

The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community. [PDF]

Clin Genet
Jain V, Radha V, Mohan V, Wakeling MN, Bennett JJ, Flanagan SE.   +5 more
europepmc   +1 more source

The association of hypertension among married Indian couples: a nationally representative cross-sectional study. [PDF]

Sci Rep
Varghese JS, Ghosh A, Stein AD, Narayan KMV, Patel SA.   +4 more
europepmc   +1 more source

Genetic counseling development and milestone in Oman. [PDF]

Genet Med Open
Al-Kharusi K, Van Wyk C, Al Hinai M, Al-Fori A, Bruwer Z.   +4 more
europepmc   +1 more source

Chudley-McCullough syndrome: A report of a rare syndromic sensorineural hearing loss. [PDF]

Radiol Case Rep
Ouqlani C, Bahlouli N, Riache H, Fikri M, Kettani NE, Jiddane M, Touarsa F.   +6 more
europepmc   +1 more source