TY - JOUR
T1 - The promise of discovering population-specific disease-associated genes in South Asia
AU - Nakatsuka, Nathan
AU - Moorjani, Priya
AU - Rai, Niraj
AU - Sarkar, Biswanath
AU - Tandon, Arti
AU - Patterson, Nick
AU - Bhavani, Gandham Srilakshmi
AU - Girisha, Katta Mohan
AU - Mustak, Mohammed S.
AU - Srinivasan, Sudha
AU - Kaushik, Amit
AU - Vahab, Saadi Abdul
AU - Jagadeesh, Sujatha M.
AU - Satyamoorthy, Kapaettu
AU - Singh, Lalji
AU - Reich, David
AU - Thangaraj, Kumarasamy
PY - 2017/9/1
Y1 - 2017/9/1
N2 - The more than 1.5 billion people who live in South Asia are correctly viewed not as a single large population but as many small endogamous groups. We assembled genome-wide data from over 2,800 individuals from over 260 distinct South Asian groups. We identified 81 unique groups, 14 of which had estimated census sizes of more than 1 million, that descend from founder events more extreme than those in Ashkenazi Jews and Finns, both of which have high rates of recessive disease due to founder events. We identified multiple examples of recessive diseases in South Asia that are the result of such founder events. This study highlights an underappreciated opportunity for decreasing disease burden among South Asians through discovery of and testing for recessive disease-associated genes.
AB - The more than 1.5 billion people who live in South Asia are correctly viewed not as a single large population but as many small endogamous groups. We assembled genome-wide data from over 2,800 individuals from over 260 distinct South Asian groups. We identified 81 unique groups, 14 of which had estimated census sizes of more than 1 million, that descend from founder events more extreme than those in Ashkenazi Jews and Finns, both of which have high rates of recessive disease due to founder events. We identified multiple examples of recessive diseases in South Asia that are the result of such founder events. This study highlights an underappreciated opportunity for decreasing disease burden among South Asians through discovery of and testing for recessive disease-associated genes.
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U2 - 10.1038/ng.3917
DO - 10.1038/ng.3917
M3 - Article
C2 - 28714977
AN - SCOPUS:85028717405
SN - 1061-4036
VL - 49
SP - 1403
EP - 1407
JO - Nature Genetics
JF - Nature Genetics
IS - 9
ER -