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
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Journal ArticleDOI
Primary congenital and developmental glaucomas.
Carly J. Lewis,Carly J. Lewis,Adam Hedberg-Buenz,Adam Hedberg-Buenz,Adam P. DeLuca,Adam P. DeLuca,Edwin M. Stone,Edwin M. Stone,Wallace L.M. Alward,Wallace L.M. Alward,John H. Fingert,John H. Fingert +11 more
TL;DR: Congenital and childhood glaucomas have strong genetic bases and disease-causing mutations have been discovered in several genes, and mutations in three genes (CYP1B1, LTBP2, TEK) have been reported in PCG patients.
Journal ArticleDOI
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Tin Aung,Tin Aung,Tin Aung,Mineo Ozaki,Takanori Mizoguchi,R. Rand Allingham,Zheng Li,Aravind Haripriya,Satoko Nakano,Steffen Uebe,Jeffrey M. Harder,Anita S Y Chan,Mei Chin Lee,Kathryn P. Burdon,Kathryn P. Burdon,Yury S. Astakhov,Khaled K. Abu-Amero,Khaled K. Abu-Amero,Juan Carlos Zenteno,Yildirim Nilgün,Tomasz Zarnowski,Mohammad Pakravan,Leen Abu Safieh,Liyun Jia,Ya Xing Wang,Susan Williams,Daniela Paoli,Patricio G. Schlottmann,Lulin Huang,Lulin Huang,Kar Seng Sim,Jia Nee Foo,Masakazu Nakano,Yoko Ikeda,Rajesh Kumar,Morio Ueno,Shin Ichi Manabe,Ken Hayashi,Shigeyasu Kazama,Ryuichi Ideta,Yosai Mori,Kazunori Miyata,Kazuhisa Sugiyama,Tomomi Higashide,Etsuo Chihara,Kenji Inoue,Satoshi Ishiko,Akitoshi Yoshida,Masahide Yanagi,Yoshiaki Kiuchi,Makoto Aihara,Tsutomu Ohashi,Toshiya Sakurai,Takako Sugimoto,Hideki Chuman,Fumihiko Matsuda,Kenji Yamashiro,Norimoto Gotoh,Masahiro Miyake,Sergei Y. Astakhov,Essam A. Osman,Saleh A. Al-Obeidan,Ohoud Owaidhah,Leyla Al-Jasim,Sami Al Shahwan,Rhys A. Fogarty,Rhys A. Fogarty,Paul Leo,Yaz Yetkin,Çilingir Ouz,Mozhgan Rezaei Kanavi,Afsaneh Nederi Beni,Shahin Yazdani,Evgeny L. Akopov,Kai Yee Toh,Kai Yee Toh,Kai Yee Toh,Gareth R. Howell,Andrew C. Orr,Yufen Goh,Wee Yang Meah,Su Qin Peh,Ewa Kosior-Jarecka,Urszula Lukasik,Mandy Krumbiegel,Eranga N. Vithana,Tien Yin Wong,Yutao Liu,Allison E. Ashley Koch,Pratap Challa,Robyn M. Rautenbach,David A. Mackey,Alex W. Hewitt,Alex W. Hewitt,Paul Mitchell,Jie Jin Wang,Jie Jin Wang,Jie Jin Wang,Ari Ziskind,Trevor R. Carmichael,Trevor R. Carmichael,Rangappa Ramakrishnan,Kalpana Narendran,Rangaraj Venkatesh,Rangaraj Venkatesh,Saravanan Vijayan,Saravanan Vijayan,Peiquan Zhao,Xueyi Chen,Dalia Guadarrama-Vallejo,Ching-Yu Cheng,Shamira A. Perera,Shamira A. Perera,Rahat Husain,Su Ling Ho,Ulrich Christoph Welge-Luessen,Christian Y. Mardin,Christian Y. Mardin,Christian Y. Mardin,Ursula Schloetzer-Schrehardt,Axel M. Hillmer,Stefan Herms,Susanne Moebus,Markus M. Nöthen,Nicole Weisschuh,Rohit Shetty,Arkasubhra Ghosh,Yik Ying Teo,Matthew A. Brown,Ignacio Lischinsky,Jonathan G Crowston,Michael Coote,Bowen Zhao,Jinghong Sang,Nihong Zhang,Qisheng You,Vera Vysochinskaya,Panayiota Founti,Anthoula Chatzikyriakidou,Alexandros Lambropoulos,E. Anastasopoulos,E. Anastasopoulos,E. Anastasopoulos,Anne L. Coleman,M. Roy Wilson,Douglas J Rhee,Jae H. Kang,Inna May-Bolchakova,Steffen Heegaard,Kazuhiko Mori,Wallace L.M. Alward,Jost B. Jonas,Liang Xu,Jeffrey M. Liebmann,Balram Chowbay,Elke Schaeffeler,Matthias Schwab,Fabian Lerner,Ningli Wang,Zhenglin Yang,Paolo Frezzotti,Shigeru Kinoshita,John H. Fingert,Masaru Inatani,Kei Tashiro,André Reis,Deepak P. Edward,Louis R. Pasquale,Toshiaki Kubota,Janey L. Wiggs,Francesca Pasutto,Fotis Topouzis,Michael V. Dubina,Jamie E Craig,Nagahisa Yoshimura,Periasamy Sundaresan,Simon W. M. John,Robert Ritch,Michael A. Hauser,Chiea Chuen Khor,Chiea Chuen Khor,Chiea Chuen Khor +181 more
TL;DR: In this paper, the authors conducted a genome-wide association study (GWAS) of 1,484 cases and 1,188 controls from Japan and followed up the most significant findings in a further 6,901 cases and 20,727 controls from 17 countries across 6 continents.
Journal ArticleDOI
Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His
Michael A. Grassi,John H. Fingert,Todd E. Scheetz,Benjamin R. Roos,Robert Ritch,Robert Ritch,Sheila K. West,Kazuhide Kawase,Abdirashid M. Shire,Robert F. Mullins,Edwin M. Stone,Edwin M. Stone +11 more
TL;DR: It is suggested that there are other yet unidentified genetic factors important in the pathogenesis of AMD that may mitigate the effects of c.1204T>C, p.Tyr402His variant.
Journal ArticleDOI
Copy Number Variations of TBK1 in Australian Patients With Primary Open-Angle Glaucoma
Mona S Awadalla,John H. Fingert,Benjamin E. Roos,Benjamin E. Roos,Simon D.M. Chen,Richard Holmes,Stuart L. Graham,Mark Chehade,Anna Galanopolous,Bronwyn Ridge,Emmanuelle Souzeau,Tiger Zhou,Owen M. Siggs,Alex W. Hewitt,David A. Mackey,Kathryn P. Burdon,Jamie E Craig +16 more
TL;DR: The presence of TBK1 copy number variations is reported in a large, well-characterized Australian cohort of patients with glaucoma, including the first example of more than 1 extra copy of this gene in glau coma patients (gene triplication).
Journal ArticleDOI
TBK1 gene duplication and normal-tension glaucoma.
Robert Ritch,Ben Darbro,Ben Darbro,Geeta Menon,Cheryl L. Khanna,Frances Solivan-Timpe,Frances Solivan-Timpe,Ben R. Roos,Ben R. Roos,Mansoor Sarfarzi,Kazuhide Kawase,Tetsuya Yamamoto,Alan L. Robin,Andrew J. Lotery,John H. Fingert,John H. Fingert +15 more
TL;DR: The identification of another case of NTG attributed to TBK1 gene duplication strengthens the case that this mutation causes glaucoma.