Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research
Over the past two decades, our understanding of Parkinson's disease (PD) has been gleaned from the discoveries made in familial and/or sporadic forms of PD in the Caucasian population. The transferability and the clinical utility of genetic discoveries to other ethnically diverse populations ar...
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2020-06-01
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Online Access: | https://www.frontiersin.org/article/10.3389/fneur.2020.00524/full |
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author |
Roopa Rajan K. P. Divya Rukmini Mridula Kandadai Ravi Yadav Venkata P. Satagopam Venkata P. Satagopam U. K. Madhusoodanan Pankaj Agarwal Niraj Kumar Teresa Ferreira Hrishikesh Kumar A. V. Sreeram Prasad Kuldeep Shetty Sahil Mehta Soaham Desai Suresh Kumar L. K. Prashanth Mohit Bhatt Pettarusp Wadia Sudha Ramalingam G. M. Wali Sanjay Pandey Felix Bartusch Maximilian Hannussek Jens Krüger Ashwin Kumar-Sreelatha Sandeep Grover Peter Lichtner Marc Sturm Jochen Roeper Volker Busskamp Giriraj R. Chandak Jens Schwamborn Pankaj Seth Thomas Gasser Olaf Riess Vinay Goyal Vinay Goyal Pramod Kumar Pal Rupam Borgohain Rejko Krüger Rejko Krüger Asha Kishore Manu Sharma The Lux-GIANT Consortium |
spellingShingle |
Roopa Rajan K. P. Divya Rukmini Mridula Kandadai Ravi Yadav Venkata P. Satagopam Venkata P. Satagopam U. K. Madhusoodanan Pankaj Agarwal Niraj Kumar Teresa Ferreira Hrishikesh Kumar A. V. Sreeram Prasad Kuldeep Shetty Sahil Mehta Soaham Desai Suresh Kumar L. K. Prashanth Mohit Bhatt Pettarusp Wadia Sudha Ramalingam G. M. Wali Sanjay Pandey Felix Bartusch Maximilian Hannussek Jens Krüger Ashwin Kumar-Sreelatha Sandeep Grover Peter Lichtner Marc Sturm Jochen Roeper Volker Busskamp Giriraj R. Chandak Jens Schwamborn Pankaj Seth Thomas Gasser Olaf Riess Vinay Goyal Vinay Goyal Pramod Kumar Pal Rupam Borgohain Rejko Krüger Rejko Krüger Asha Kishore Manu Sharma The Lux-GIANT Consortium Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research Frontiers in Neurology Parkinson's disease genetic diversity genome-wide association study common genetic variation biobank |
author_facet |
Roopa Rajan K. P. Divya Rukmini Mridula Kandadai Ravi Yadav Venkata P. Satagopam Venkata P. Satagopam U. K. Madhusoodanan Pankaj Agarwal Niraj Kumar Teresa Ferreira Hrishikesh Kumar A. V. Sreeram Prasad Kuldeep Shetty Sahil Mehta Soaham Desai Suresh Kumar L. K. Prashanth Mohit Bhatt Pettarusp Wadia Sudha Ramalingam G. M. Wali Sanjay Pandey Felix Bartusch Maximilian Hannussek Jens Krüger Ashwin Kumar-Sreelatha Sandeep Grover Peter Lichtner Marc Sturm Jochen Roeper Volker Busskamp Giriraj R. Chandak Jens Schwamborn Pankaj Seth Thomas Gasser Olaf Riess Vinay Goyal Vinay Goyal Pramod Kumar Pal Rupam Borgohain Rejko Krüger Rejko Krüger Asha Kishore Manu Sharma The Lux-GIANT Consortium |
author_sort |
Roopa Rajan |
title |
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research |
title_short |
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research |
title_full |
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research |
title_fullStr |
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research |
title_full_unstemmed |
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research |
title_sort |
genetic architecture of parkinson's disease in the indian population: harnessing genetic diversity to address critical gaps in parkinson's disease research |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neurology |
issn |
1664-2295 |
publishDate |
2020-06-01 |
description |
Over the past two decades, our understanding of Parkinson's disease (PD) has been gleaned from the discoveries made in familial and/or sporadic forms of PD in the Caucasian population. The transferability and the clinical utility of genetic discoveries to other ethnically diverse populations are unknown. The Indian population has been under-represented in PD research. The Genetic Architecture of PD in India (GAP-India) project aims to develop one of the largest clinical/genomic bio-bank for PD in India. Specifically, GAP-India project aims to: (1) develop a pan-Indian deeply phenotyped clinical repository of Indian PD patients; (2) perform whole-genome sequencing in 500 PD samples to catalog Indian genetic variability and to develop an Indian PD map for the scientific community; (3) perform a genome-wide association study to identify novel loci for PD and (4) develop a user-friendly web-portal to disseminate results for the scientific community. Our “hub-spoke” model follows an integrative approach to develop a pan-Indian outreach to develop a comprehensive cohort for PD research in India. The alignment of standard operating procedures for recruiting patients and collecting biospecimens with international standards ensures harmonization of data/bio-specimen collection at the beginning and also ensures stringent quality control parameters for sample processing. Data sharing and protection policies follow the guidelines established by local and national authorities.We are currently in the recruitment phase targeting recruitment of 10,200 PD patients and 10,200 healthy volunteers by the end of 2020. GAP-India project after its completion will fill a critical gap that exists in PD research and will contribute a comprehensive genetic catalog of the Indian PD population to identify novel targets for PD. |
topic |
Parkinson's disease genetic diversity genome-wide association study common genetic variation biobank |
url |
https://www.frontiersin.org/article/10.3389/fneur.2020.00524/full |
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doaj-3268a466280148719c06966c967d74362020-11-25T03:18:50ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-06-011110.3389/fneur.2020.00524531997Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease ResearchRoopa Rajan0K. P. Divya1Rukmini Mridula Kandadai2Ravi Yadav3Venkata P. Satagopam4Venkata P. Satagopam5U. K. Madhusoodanan6Pankaj Agarwal7Niraj Kumar8Teresa Ferreira9Hrishikesh Kumar10A. V. Sreeram Prasad11Kuldeep Shetty12Sahil Mehta13Soaham Desai14Suresh Kumar15L. K. Prashanth16Mohit Bhatt17Pettarusp Wadia18Sudha Ramalingam19G. M. Wali20Sanjay Pandey21Felix Bartusch22Maximilian Hannussek23Jens Krüger24Ashwin Kumar-Sreelatha25Sandeep Grover26Peter Lichtner27Marc Sturm28Jochen Roeper29Volker Busskamp30Giriraj R. Chandak31Jens Schwamborn32Pankaj Seth33Thomas Gasser34Olaf Riess35Vinay Goyal36Vinay Goyal37Pramod Kumar Pal38Rupam Borgohain39Rejko Krüger40Rejko Krüger41Asha Kishore42Manu Sharma43The Lux-GIANT ConsortiumDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, IndiaSree Chitra Tirunal Institute for Medical Sciences, Trivandrum, IndiaDepartment of Neurology, Nizam's Institute of Medical Sciences, Hyderabad, IndiaNational Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, IndiaLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg, LuxembourgELIXIR-Luxembourg Node, Belvaux, LuxembourgSree Chitra Tirunal Institute for Medical Sciences, Trivandrum, IndiaMovement Disorders Clinic, Global Hospitals, Mumbai, IndiaAll India Institute of Medical Sciences, Rishikesh, IndiaGoa Medical College, Panaji, India0Institute of Neurosciences, Kolkata, India1Lourdes Hospital, Kochi, India2Narayana Hrudayalaya Multispeciality Hospital, Bangalore, India3Department of Neurology, PGIMER, Chandigarh, India4Shree Krishna Hospital and Pramukhswami Medical College, Karamsad, India5Department of Neurology, Vijaya Health Centre, Chennai, India6Center for Parkinson's Disease and Movement Disorders, Vikram Hospital, Bangalore, India7Kokilaben Dhirubhai Ambani Hospital, Mumbai, India8Jaslok Hospital, Mumbai, India9Department of Community Medicine, PSG Institute of Medical Sciences and Research, Coimbatore, India0Neurospecialities Centre, Belgaum, India1Department of Neurology, G. B. Pant Institute of Medical Education and Research, New Delhi, India2Zentrum für Datenverarbeitung (ZDV), University of Tubingen, Tübingen, Germany2Zentrum für Datenverarbeitung (ZDV), University of Tubingen, Tübingen, Germany2Zentrum für Datenverarbeitung (ZDV), University of Tubingen, Tübingen, Germany3Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tubingen, Tübingen, Germany3Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tubingen, Tübingen, Germany4Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Human Genetics, Neuherberg, Germany5Institute for Medical Genetics and Applied Genomics, University of Tubingen, Tübingen, Germany6Institute of Neurophysiology, Goethe University Frankfurt, Frankfurt, Germany7Department of Ophthalmology, Universitäts-Augenklinik Bonn, University of Bonn, Bonn, Germany8Centre for Cellular and Molecular Biology, Hyderabad, IndiaLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg, Luxembourg9National Brain Research Centre, Gurugram, India0Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany5Institute for Medical Genetics and Applied Genomics, University of Tubingen, Tübingen, GermanyDepartment of Neurology, All India Institute of Medical Sciences, New Delhi, India1Medanta the Medicity, Gurgaon, IndiaNational Institute of Mental Health and Neurosciences (NIMHANS), Bengaluru, IndiaDepartment of Neurology, Nizam's Institute of Medical Sciences, Hyderabad, IndiaLuxembourg Centre for Systems Biomedicine, University of Luxembourg, Luxembourg, Luxembourg2Transversal Translational Medicine, Luxembourg Institute of Health (LIH), Strassen, LuxembourgSree Chitra Tirunal Institute for Medical Sciences, Trivandrum, India3Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tubingen, Tübingen, GermanyOver the past two decades, our understanding of Parkinson's disease (PD) has been gleaned from the discoveries made in familial and/or sporadic forms of PD in the Caucasian population. The transferability and the clinical utility of genetic discoveries to other ethnically diverse populations are unknown. The Indian population has been under-represented in PD research. The Genetic Architecture of PD in India (GAP-India) project aims to develop one of the largest clinical/genomic bio-bank for PD in India. Specifically, GAP-India project aims to: (1) develop a pan-Indian deeply phenotyped clinical repository of Indian PD patients; (2) perform whole-genome sequencing in 500 PD samples to catalog Indian genetic variability and to develop an Indian PD map for the scientific community; (3) perform a genome-wide association study to identify novel loci for PD and (4) develop a user-friendly web-portal to disseminate results for the scientific community. Our “hub-spoke” model follows an integrative approach to develop a pan-Indian outreach to develop a comprehensive cohort for PD research in India. The alignment of standard operating procedures for recruiting patients and collecting biospecimens with international standards ensures harmonization of data/bio-specimen collection at the beginning and also ensures stringent quality control parameters for sample processing. Data sharing and protection policies follow the guidelines established by local and national authorities.We are currently in the recruitment phase targeting recruitment of 10,200 PD patients and 10,200 healthy volunteers by the end of 2020. GAP-India project after its completion will fill a critical gap that exists in PD research and will contribute a comprehensive genetic catalog of the Indian PD population to identify novel targets for PD.https://www.frontiersin.org/article/10.3389/fneur.2020.00524/fullParkinson's diseasegenetic diversitygenome-wide association studycommon genetic variationbiobank |