J
John H. Fingert
Researcher at University of Iowa
Publications - 171
Citations - 14975
John H. Fingert is an academic researcher from University of Iowa. The author has contributed to research in topics: Glaucoma & Myocilin. The author has an hindex of 47, co-authored 165 publications receiving 13442 citations. Previous affiliations of John H. Fingert include University of Arkansas for Medical Sciences & University of Iowa Hospitals and Clinics.
Papers
More filters
Journal ArticleDOI
LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States.
John H. Fingert,Wallace L.M. Alward,Young H. Kwon,Kai Wang,Luan M. Streb,Val C. Sheffield,Edwin M. Stone +6 more
Journal ArticleDOI
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci
Tin Aung,Tin Aung,Mineo Ozaki,Mei Chin Lee,Ursula Schlötzer-Schrehardt,Gudmar Thorleifsson,Takanori Mizoguchi,Robert P. Igo,Aravind Haripriya,Susan Williams,Yury S. Astakhov,Andrew C. Orr,Kathryn P. Burdon,Kathryn P. Burdon,Satoko Nakano,Kazuhiko Mori,Khaled K. Abu-Amero,Khaled K. Abu-Amero,Michael A. Hauser,Zheng Li,Gopalakrishnan Prakadeeswari,Jessica N. Cooke Bailey,Alina Popa Cherecheanu,Jae H. Kang,Sarah C. Nelson,Ken Hayashi,Shin-ichi Manabe,Shigeyasu Kazama,Tomasz Zarnowski,Kenji Inoue,Murat Irkec,Miguel Coca-Prados,Miguel Coca-Prados,Kazuhisa Sugiyama,Irma Järvelä,Patricio G. Schlottmann,S Fabian Lerner,Hasnaa Lamari,Yildirim Nilgün,Mukharram M. Bikbov,Ki Ho Park,Soon Cheol Cha,Kenji Yamashiro,Juan Carlos Zenteno,Jost B. Jonas,Jost B. Jonas,Rajesh Kumar,Shamira A. Perera,Anita S Y Chan,Anita S Y Chan,Nino Kobakhidze,Ronnie George,Lingam Vijaya,Tan Do,Deepak P. Edward,Lourdes de Juan Marcos,Mohammad Pakravan,Sasan Moghimi,Ryuichi Ideta,Daniella Bach-Holm,Per Kappelgaard,Barbara M Wirostko,Scott Thomas,Daniel Gaston,Karen Bedard,Wenda L. Greer,Zhenglin Yang,Xueyi Chen,Lulin Huang,Lulin Huang,Jinghong Sang,Hongyan Jia,Liyun Jia,Chunyan Qiao,Hui Zhang,Xuyang Liu,Bowen Zhao,Ya Xing Wang,Liang Xu,Stéphanie Leruez,Pascal Reynier,George Chichua,Sergo Tabagari,Steffen Uebe,Matthias Zenkel,Daniel Berner,Georg Mossböck,Nicole Weisschuh,Ursula Hoja,Ulrich-Christoph Welge-Luessen,Christian Y. Mardin,Panayiota Founti,Anthi Chatzikyriakidou,Theofanis Pappas,Eleftherios Anastasopoulos,Alexandros Lambropoulos,Arkasubhra Ghosh,Rohit Shetty,Natalia Porporato,Vijayan Saravanan,Rengaraj Venkatesh,Chandrashekaran Shivkumar,N Kalpana,Sripriya Sarangapani,Mozhgan Rezaei Kanavi,Afsaneh Naderi Beni,Shahin Yazdani,Alireza Lashay,Homa Naderifar,Nassim Khatibi,Antonio Maria Fea,Carlo Lavia,Laura Dallorto,Teresa Rolle,Paolo Frezzotti,Daniela Paoli,Erika Salvi,Paolo Manunta,Yosai Mori,Kazunori Miyata,Tomomi Higashide,Etsuo Chihara,Satoshi Ishiko,Akitoshi Yoshida,Masahide Yanagi,Yoshiaki Kiuchi,Tsutomu Ohashi,Toshiya Sakurai,Takako Sugimoto,Hideki Chuman,Makoto Aihara,Masaru Inatani,Masahiro Miyake,Norimoto Gotoh,Fumihiko Matsuda,Nagahisa Yoshimura,Yoko Ikeda,Morio Ueno,Chie Sotozono,Jin Wook Jeoung,Min Sagong,Kyu Hyung Park,Jeeyun Ahn,Marisa Cruz-Aguilar,Sidi M Ezzouhairi,Abderrahman Rafei,Yaan Fun Chong,Xiao Yu Ng,Shuang Ru Goh,Yueming Chen,Victor H. K. Yong,Muhammad Imran Khan,Olusola Olawoye,Olusola Olawoye,Adeyinka O. Ashaye,Adeyinka O. Ashaye,Idakwo Ugbede,Adeola O Onakoya,Adeola O Onakoya,Nkiru Kizor-Akaraiwe,Chaiwat Teekhasaenee,Yanin Suwan,Wasu Supakontanasan,Suhanya Okeke,Nkechi J Uche,Ifeoma N. Asimadu,Humaira Ayub,Farah Akhtar,Ewa Kosior-Jarecka,Urszula Lukasik,Ignacio Lischinsky,Vania Castro,Rodolfo Perez Grossmann,Gordana Sunaric Megevand,Sylvain Roy,Edward Dervan,Eoin Silke,Aparna Rao,Priti Sahay,Pablo Fornero,Osvaldo Cuello,Delia Sivori,Tamara Zompa,Richard A. Mills,Emmanuelle Souzeau,Paul Mitchell,Jie Jin Wang,Alex W. Hewitt,Alex W. Hewitt,Michael Coote,Jonathan G Crowston,Sergei Y. Astakhov,Eugeny L. Akopov,A. Emelyanov,A. Emelyanov,Vera Vysochinskaya,Gyulli M. Kazakbaeva,R.R. Fayzrakhmanov,Saleh A. Al-Obeidan,Ohoud Owaidhah,Leyla Al-Jasim,Balram Chowbay,Balram Chowbay,Jia Nee Foo,Jia Nee Foo,Raphael Q Soh,Kar Seng Sim,Z. Xie,Augustine W O Cheong,Shi Qi Mok,Hui Meng Soo,Xiao Yin Chen,Su Qin Peh,Khai Koon Heng,Rahat Husain,Su-Ling Ho,Axel M. Hillmer,Ching-Yu Cheng,Francisco A. Escudero-Domínguez,Rogelio González-Sarmiento,Frederico Martinon-Torres,Antonio Salas,Kessara Pathanapitoon,Linda Hansapinyo,Boonsong Wanichwecharugruang,Naris Kitnarong,Anavaj Sakuntabhai,Anavaj Sakuntabhai,Hip X Nguyn,Giang T T Nguyn,Trình V Nguyn,Werner Zenz,A. Binder,DS Klobassa,Martin L. Hibberd,Martin L. Hibberd,Sonia Davila,Stefan Herms,Stefan Herms,Stefan Herms,Markus M. Nöthen,Susanne Moebus,Robyn M. Rautenbach,Ari Ziskind,Trevor R. Carmichael,Michèle Ramsay,Lydia Álvarez,Montserrat García,Héctor González-Iglesias,Pedro Pablo Rodríguez-Calvo,Luis Fernández-Vega Cueto,Çilingir Oguz,Nevbahar Tamçelik,Eray Atalay,Bilge Batu,Dilek Aktas,Burcu Kasım,M. Roy Wilson,Anne L. Coleman,Yutao Liu,Pratap Challa,Leon W. Herndon,Rachel W. Kuchtey,John Kuchtey,Karen Curtin,Craig J. Chaya,Alan S. Crandall,Linda M. Zangwill,Tien Yin Wong,Tien Yin Wong,Masakazu Nakano,Shigeru Kinoshita,Anneke I. den Hollander,Eija Vesti,John H. Fingert,John H. Fingert,Richard K. Lee,Arthur J. Sit,Bradford J. Shingleton,Ningli Wang,Daniele Cusi,Raheel Qamar,Raheel Qamar,Peter Kraft,Margaret A. Pericak-Vance,Soumya Raychaudhuri,Steffen Heegaard,Tero Kivelä,André Reis,Friedrich E. Kruse,Robert N. Weinreb,Louis R. Pasquale,Louis R. Pasquale,Jonathan L. Haines,Unnur Thorsteinsdottir,Unnur Thorsteinsdottir,Fridbert Jonasson,R. Rand Allingham,Dan Milea,Dan Milea,Robert Ritch,Toshiaki Kubota,Kei Tashiro,Eranga N. Vithana,Shazia Micheal,Fotis Topouzis,Jamie E Craig,Michael V. Dubina,Michael V. Dubina,Periasamy Sundaresan,Kari Stefansson,Kari Stefansson,Janey L. Wiggs,Francesca Pasutto,Chiea Chuen Khor,Chiea Chuen Khor +315 more
TL;DR: A rare protective allele at LOXL1 is identified through deep resequencing of XFS cases and controls and a potential role for naturally occurring rare LO XL1 variants in disease biology is highlighted.
Journal ArticleDOI
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.
Suma P. Shankar,John H. Fingert,Valerio Carelli,Maria Lucia Valentino,Terri M. King,Stephen P. Daiger,Solange Rios Salomão,Adriana Berezovsky,Rubens Belfort,Terri A. Braun,Val C. Sheffield,Val C. Sheffield,Alfredo A. Sadun,Edwin M. Stone,Edwin M. Stone +14 more
TL;DR: X-chromosomal linkage analysis in a large Brazilian family harboring a homoplasmic G11778A mtDNA mutation on a haplogroup J background suggests genetic heterogeneity for X-linked modifiers of LHON.
Journal ArticleDOI
Evidence for Genetic Heterogeneity within Eight Glaucoma Families, with the GLC1A Gln368STOP Mutation Being an Important Phenotypic Modifier
Jamie E Craig,Jamie E Craig,Paul N. Baird,Paul N. Baird,Danielle L. Healey,Andrew I McNaught,Andrew I McNaught,Paul J. McCartney,Julian L Rait,Joanne L. Dickinson,Lynne Roe,John H. Fingert,Edwin M. Stone,David A. Mackey,David A. Mackey +14 more
TL;DR: In this paper, the authors investigated the phenotype and age-related penetrance of primary open-angle glaucoma (POAG) in Australian families with the most common Myocilin mutation (Gln368STOP).
Journal ArticleDOI
North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13
Kent W. Small,Adam P. DeLuca,S. Scott Whitmore,Thomas Rosenberg,Rosemary Silva-Garcia,Nitin Udar,Bernard Puech,Charles A. Garcia,Thomas A. Rice,Gerald A. Fishman,Elise Héon,James C. Folk,Luan M. Streb,Christine M. Haas,Luke A Wiley,Todd E. Scheetz,John H. Fingert,Robert F. Mullins,Budd A. Tucker,Edwin M. Stone +19 more
TL;DR: Four of these strongly implicate the involvement of PRDM13 in macular development, whereas the pathophysiologic mechanism of the fifth remains unknown but may involve the developmental dysregulation of IRX1.