Excess of rare noncoding variants in several type 2 diabetes candidate genes among Asian Indian families

The high burden of T2D in these families may stem from the enrichment of noncoding RVs in a small number of major known genes (including MODY genes) with oligogenic inheritance alongside RVs from genes associated with polygenic susceptibility. These findings highlight the need to conduct deeper evaluations of families from non-European ancestries to identify potential novel therapeutics and implement preventative strategies.

Authors

Institutions

Publication Details

Journal
Communications Medicine
Published
2025-02-22
DOI
https://doi.org/10.1038/s43856-025-00750-9
Citations
2
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
3.63

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Excess of rare noncoding variants in several type 2 diabetes candidate genes among Asian Indian families

John Blangero, Deepika Ramu, Dharambir K. Sanghera, Teena Koshy et al.
2 citations
Communications Medicine
Genetic Associations and Epidemiology
3.63
article

Excess of rare noncoding variants in several type 2 diabetes candidate genes among Asian Indian families

John Blangero, Deepika Ramu, Dharambir K. Sanghera, Teena Koshy, Juan Carlos López-Alvarenga, Umarani Ravichandran, Sadagopan Thanikachalam, Srinivas Mummidi, Marcio Almeida, R Parthasarathy, Juliet A. Ezeilo, Gurpreet Singh Wander, Piers R. Blackett, Christopher E. Aston, Mahaboob Vali Shaik, Ravindranath Duggirala, Roy G. Resendez, Krishna Mohan Medicherla, Thyagarajan Sadras Panchatcharam, Solomon F.D. Paul, Priyanka Venugopal, Sailesh Lodha, Dileep Kumar K, Madhusmita Rout, S. NOELTA, Rajeev Gupta, Natesan Chidambaram, Vettriselvi Venkatesan, Rector Arya, Krishna Kumar Sharma, Asish K. Ghosh, Surendra K. Sharma, N. K. Mehra, Sarju Ralhan, Jai Rup Singh, Amaresh Reddy ­Ponnala, Juan Paralta, Mendez Mariana
article en
2 citations

Abstract

The high burden of T2D in these families may stem from the enrichment of noncoding RVs in a small number of major known genes (including MODY genes) with oligogenic inheritance alongside RVs from genes associated with polygenic susceptibility. These findings highlight the need to conduct deeper evaluations of families from non-European ancestries to identify potential novel therapeutics and implement preventative strategies.

Communications MedicineVol. 5(1)
Texas A&M University – San Antonio (US), Guru Nanak Dev University (IN), Annamalai University (IN), Sri Ramachandra Institute of Higher Education and Research (IN), The University of Texas Rio Grande Valley (US), Rajasthan University of Health Sciences (IN), Dayanand Medical College & Hospital (IN), Krishna Institute of Medical Sciences (IN), Narayana Dental College and Hospital (IN), Birla Institute of Scientific Research (IN), Eternal Hospital (IN), University of Oklahoma Health Sciences Center (US), All India Institute of Medical Sciences (IN)
Foundation for the National Institutes of Health, Presbyterian Health Foundation, Indian Council of Medical Research, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 9%
Genetic Associations and Epidemiology
3.63
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.