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Page 1
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
Wall JD, Sathirapongsasuti JF, Gupta R, Rasheed A, Venkatesan R, Belsare S, Menon R, Phalke S, Mittal A, Fang J, Tanneeru D, Deshmukh M, Bassi A, Robinson J, Chaudhary R, Murugan S, Ul-Asar Z, Saleem I, Ishtiaq U, Fatima A, Sheikh SS, Hameed S, Ishaq M, Rasheed SZ, Memon FU, Jalal A, Abbas S, Frossard P, Fuchsberger C, Forer L, Schoenherr S, Bei Q, Bhangale T, Tom J, Gadde SGK, B V P, Naik NK, Wang M, Kwok PY, Khera AV, Lakshmi BR, Butterworth AS, Chowdhury R, Danesh J, di Angelantonio E, Naheed A, Goyal V, Kandadai RM, Kumar H, Borgohain R, Mukherjee A, Wadia PM, Yadav R, Desai S, Kumar N, Biswas A, Pal PK, Muthane UB, Das SK, Ramprasad VL, Kukkle PL, Seshagiri S, Kathiresan S, Ghosh A, Mohan V, Saleheen D, Stawiski EW, Peterson AS. Wall JD, et al. Among authors: muthane ub. Nat Commun. 2023 Jun 8;14(1):3377. doi: 10.1038/s41467-023-38766-1. Nat Commun. 2023. PMID: 37291107 Free PMC article.
Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.
Kukkle PL, Geetha TS, Chaudhary R, Sathirapongsasuti JF, Goyal V, Kandadai RM, Kumar H, Borgohain R, Mukherjee A, Oliver M, Sunil M, Mootor MFE, Kapil S, Mandloi N, Wadia PM, Yadav R, Desai S, Kumar N, Biswas A, Pal PK, Muthane UB, Das SK, Sakthivel Murugan SM, Peterson AS, Stawiski EW, Seshagiri S, Gupta R, Ramprasad VL, Prai PRAOI. Kukkle PL, et al. Among authors: muthane ub. Adv Biol (Weinh). 2022 Nov;6(11):e2101326. doi: 10.1002/adbi.202101326. Epub 2022 Jul 10. Adv Biol (Weinh). 2022. PMID: 35810474
Early Onset Parkinson's disease due to DJ1 mutations: An Indian study.
Abbas MM, Govindappa ST, Sudhaman S, Thelma BK, Juyal RC, Behari M, Muthane UB. Abbas MM, et al. Among authors: muthane ub. Parkinsonism Relat Disord. 2016 Nov;32:20-24. doi: 10.1016/j.parkreldis.2016.04.024. Epub 2016 Apr 24. Parkinsonism Relat Disord. 2016. PMID: 27592010
Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation.
Abbas MM, Govindappa ST, Sheerin UM, Bhatia KP, Muthane UB. Abbas MM, et al. Among authors: muthane ub. Mov Disord Clin Pract. 2016 Apr 26;4(1):132-135. doi: 10.1002/mdc3.12353. eCollection 2017 Jan-Feb. Mov Disord Clin Pract. 2016. PMID: 30713959 Free PMC article. No abstract available.
Secondary parkinsonism with Mumps infection.
Abbas MM, Basu P, Reginald V, Kumar RH, Muthane UB. Abbas MM, et al. Among authors: muthane ub. Parkinsonism Relat Disord. 2015 Oct;21(10):1288-9. doi: 10.1016/j.parkreldis.2015.08.028. Epub 2015 Aug 28. Parkinsonism Relat Disord. 2015. PMID: 26324210 No abstract available.
Parkinsonism Hyperpyrexia Syndrome following Deep Brain Stimulation.
Govindappa ST, Abbas MM, Hosurkar G, Varma RG, Muthane UB. Govindappa ST, et al. Among authors: muthane ub. Parkinsonism Relat Disord. 2015 Oct;21(10):1284-5. doi: 10.1016/j.parkreldis.2015.08.004. Epub 2015 Aug 11. Parkinsonism Relat Disord. 2015. PMID: 26298388 No abstract available.
45 results