J
Jinhui Ding
Researcher at National Institutes of Health
Publications - 99
Citations - 11102
Jinhui Ding is an academic researcher from National Institutes of Health. The author has contributed to research in topics: LRRK2 & Gene. The author has an hindex of 34, co-authored 90 publications receiving 9341 citations. Previous affiliations of Jinhui Ding include Arizona State University.
Papers
More filters
Journal ArticleDOI
The Parkinson's Disease DNA Variant Browser
Jonggeol J. Kim,Jonggeol J. Kim,Mary B. Makarious,Sara Bandres-Ciga,J. R. Gibbs,Jinhui Ding,Dena G. Hernandez,Janet Brooks,Francis P. Grenn,Hirotaka Iwaki,Andrew B. Singleton,Mike A. Nalls,Cornelis Blauwendraat +12 more
TL;DR: The Parkinson's Disease Sequencing Browser as mentioned in this paper is a web application that presents summary-level frequency data from multiple large-scale genotyping and sequencing projects, including 28,453 cases, 1650 proxy cases, and 72,024 controls.
Journal ArticleDOI
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies.
Cornelis Blauwendraat,Mike A. Nalls,Monica Federoff,Olga Pletnikova,Jinhui Ding,Christopher Letson,Joshua T. Geiger,J. Raphael Gibbs,Dena G. Hernandez,Dena G. Hernandez,Juan C. Troncoso,Javier Simón-Sánchez,Javier Simón-Sánchez,Sonja W. Scholz,Sonja W. Scholz +14 more
TL;DR: A homozygous missense mutation in the adenosine A1 receptor gene (ADORA1) in an autosomal-recessive, early-onset, L-doparesponsive, consanguineous Iranian family with parkinsonism and cognitive decline is identified.
Journal ArticleDOI
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease.
Alexey A. Shadrin,Sören Mucha,David Ellinghaus,Mary B. Makarious,Cornelis Blauwendraat,Ashwin Ashok Kumar Sreelatha,Antonio Heras-Garvin,Jinhui Ding,Monia B. Hammer,Alexandra Foubert-Samier,Wassilios G. Meissner,Olivier Rascol,Anne Pavy-Le Traon,Oleksandr Frei,Kevin S. O’Connell,Shahram Bahrami,Stefan Schreiber,Wolfgang Lieb,Martina Müller-Nurasyid,Ulf Schminke,Georg Homuth,Carsten Oliver Schmidt,Markus M. Nöthen,Per Hoffmann,Christian Gieger,Gregor K. Wenning,J. Raphael Gibbs,Andre Franke,John Hardy,Nadia Stefanova,Thomas Gasser,Thomas Gasser,Andrew B. Singleton,Henry Houlden,Sonja W. Scholz,Sonja W. Scholz,Ole A. Andreassen,Manu Sharma +37 more
TL;DR: This work aimed to investigate genetic overlap between MSA and 7 autoimmune diseases and to identify shared genetic loci and to investigate shared Genetic loci of MSA patients with known autoimmune diseases.
Posted ContentDOI
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture
Ruth Chia,Marya S. Sabir,Sara Bandres-Ciga,Sara Saez-Atienzar,Regina H. Reynolds,Regina H. Reynolds,Regina H. Reynolds,Emil K. Gustavsson,Emil K. Gustavsson,Ronald L. Walton,Samreen Ahmed,Coralie Viollet,Jinhui Ding,Mary B. Makarious,Monica Diez-Fairen,Makayla K. Portley,Zalak Shah,Yevgeniya Abramzon,Dena G. Hernandez,Cornelis Blauwendraat,David J. Stone,John D. Eicher,Laura Parkkinen,Olaf Ansorge,Lorraine N. Clark,Lawrence S. Honig,Karen Marder,Afina W. Lemstra,Peter St George-Hyslop,Peter St George-Hyslop,Elisabet Londos,Kevin Morgan,Tammaryn Lashley,Thomas T. Warner,Zane Jaunmuktane,Douglas Galasko,Douglas Galasko,Isabel Santana,Pentti J. Tienari,Liisa Myllykangas,Minna Oinas,Nigel J. Cairns,John C. Morris,Glenda M. Halliday,Glenda M. Halliday,Glenda M. Halliday,Vivianna M. Van Deerlin,John Q. Trojanowski,Maurizio Grassano,Maurizio Grassano,Andrea Calvo,Gabriele Mora,Antonio Canosa,Gianluca Floris,Ryan C. Bohannan,Francesca Brett,Ziv Gan-Or,Joshua T. Geiger,Anni Moore,Patrick May,Rejko Krüger,Rejko Krüger,David Goldstein,Grisel Lopez,Nahid Tayebi,Ellen Sidransky,Lucy Norcliffe-Kaufmann,Jose-Alberto Palma,Horacio Kaufmann,Vikram Shakkottai,Matthew H. Perkins,Kathy L. Newell,Thomas Gasser,Claudia Schulte,Francesco Landi,Erika Salvi,Daniele Cusi,Eliezer Masliah,Ronald C. Kim,Chad A. Caraway,Ed Monuki,Maura Brunetti,Ted M. Dawson,Liana S. Rosenthal,Marilyn S. Albert,Olga Pletnikova,Juan C. Troncoso,Margaret E. Flanagan,Qinwen Mao,Eileen H. Bigio,Eloy Rodríguez-Rodríguez,Jon Infante,Carmen Lage,Isabel González-Aramburu,Pascual Sanchez-Juan,Bernardino Ghetti,Julia Keith,Sandra E. Black,Mario Masellis,Ekaterina Rogaeva,Charles Duyckaerts,Alexis Brice,Suzanne Lesage,G. Xiromerisiou,Matthew J. Barrett,Bension S. Tilley,Steve M. Gentleman,Giancarlo Logroscino,Geidy E. Serrano,Thomas G. Beach,Ian G. McKeith,Alan J. Thomas,Johannes Attems,Christopher M. Morris,Laura Palmer,Seth Love,Claire Troakes,Safa Al-Sarraj,Angela K. Hodges,Dag Aarsland,Gregory Klein,Scott M. Kaiser,Randy Woltjer,Pau Pastor,Lynn M. Bekris,James B. Leverenz,Lilah M. Besser,Amanda B. Kuzma,Alan E. Renton,Alison Goate,David A. Bennett,Clemens R. Scherzer,Huw R. Morris,Raffaele Ferrari,Diego Albani,Stuart Pickering Brown,Kelley Faber,Kelley Faber,Walter A. Kukull,Estrella Morenas-Rodríguez,Alberto Lleó,Juan Fortea,Daniel Alcolea,Jordi Clarimón,Mike A. Nalls,Luigi Ferrucci,Susan M. Resnick,Toshiko Tanaka,Tatiana Foroud,Neill R. Graff-Radford,Zbigniew K. Wszolek,Tanis J. Ferman,Bradley F. Boeve,John Hardy,Eric Topol,Ali Torkamani,Ali Torkamani,Andrew B. Singleton,M. Ryten,Dennis W. Dickson,Adriano Chiò,Owen A. Ross,J. Raphael Gibbs,J. Raphael Gibbs,Clifton L. Dalgard,Bryan J. Traynor,Sonja W. Scholz +166 more
TL;DR: Genetic risk scores demonstrate that LBD shares risk profiles and pathways with Alzheimer's and Parkinson’s disease, providing a deeper molecular understanding of the complex genetic architecture of this age-related neurodegenerative condition.
Posted ContentDOI
The Parkinson’s Disease DNA Variant Browser
Jonggeol J. Kim,Mary B. Makarious,Sara Bandres-Ciga,J. Raphael Gibbs,Jinhui Ding,Dena G. Hernandez,Janet Brooks,Francis P. Grenn,Hirotaka Iwaki,Andrew B. Singleton,Mike A. Nalls,Cornelis Blauwendraat +11 more
TL;DR: The Parkinson's Disease Sequencing Browser is a Shiny-based web application that presents comprehensive summary-level frequency data from multiple large-scale genotyping and sequencing projects to assist researchers on their search for PD-risk genes and variant candidates.