Jia-Nee Foo

Jia-Nee Foo

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Jia-Nee Foo

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Polycystic kidney disease: new knowledge and future promises.

Authors:
Jia Nee Foo Yun Xia

Curr Opin Genet Dev 2019 Aug 30;56:69-75. Epub 2019 Aug 30.

Lee Kong Chian School of Medicine, Nanyang Technological University Singapore, 11 Mandalay Road, 308232, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.gde.2019.06.007DOI Listing
August 2019

A recurrent missense mutation in the EDAR gene causes severe autosomal recessive hypohidrotic ectodermal dysplasia in two consanguineous Kashmiri families.

J Gene Med 2019 Jul 16:e3113. Epub 2019 Jul 16.

Department of Biotechnology, University of Azad Jammu and Kashmir, Muzaffarabad, Pakistan.

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http://dx.doi.org/10.1002/jgm.3113DOI Listing
July 2019

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta.

J Biomed Sci 2019 04 28;26(1):31. Epub 2019 Apr 28.

Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-AzamUniversity, University Road, Islamabad, 45320, Pakistan.

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http://dx.doi.org/10.1186/s12929-019-0525-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487057PMC
April 2019

Evaluation of novel Parkinson's disease candidate genes in the Chinese population.

Neurobiol Aging 2019 02 21;74:235.e1-235.e4. Epub 2018 Sep 21.

Department of Neurology, National Neuroscience Institute, Singapore, Singapore; Duke-National University of Singapore Medical School, Singapore, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2018.09.013DOI Listing
February 2019

ITPKB and ZNF184 are associated with Parkinson's disease risk in East Asians.

Neurobiol Aging 2019 Feb 2. Epub 2019 Feb 2.

Department of Neurology, National Neuroscience Institute, Singapore, Singapore; Duke-National University of Singapore Medical School, Singapore, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2019.01.026DOI Listing
February 2019

Parkinson's disease GWAS-linked Park16 carriers show greater motor progression.

J Med Genet 2019 Feb 27. Epub 2019 Feb 27.

Department of Neurology, National Neuroscience Institute, Singapore general hospital campus, Singapore, Singapore.

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http://dx.doi.org/10.1136/jmedgenet-2018-105661DOI Listing
February 2019

Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta.

J Biomed Sci 2018 Nov 17;25(1):82. Epub 2018 Nov 17.

Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, University Road, Islamabad, Post code 45320, Pakistan.

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https://jbiomedsci.biomedcentral.com/articles/10.1186/s12929
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http://dx.doi.org/10.1186/s12929-018-0481-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240425PMC
November 2018

Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement.

Neurobiol Aging 2018 08 16;68:160.e15-160.e19. Epub 2018 Apr 16.

Department of Neurology, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore; Duke-NUS Graduate Medical School, Singapore.

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https://linkinghub.elsevier.com/retrieve/pii/S01974580183012
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http://dx.doi.org/10.1016/j.neurobiolaging.2018.04.003DOI Listing
August 2018

Identifying genes in Parkinson disease: state of the art.

Med J Aust 2018 05;208(9):381-382

National Neuroscience Institute, Singapore.

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May 2018

ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis.

J Invest Dermatol 2018 02 28;138(2):291-300. Epub 2017 Sep 28.

Laboratory of Human Genetics and Embryology, Institute of Medical Biology, A*STAR, Singapore, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2017.08.045DOI Listing
February 2018

Genome-Wide Analysis of Protein-Coding Variants in Leprosy.

J Invest Dermatol 2017 12 24;137(12):2544-2551. Epub 2017 Aug 24.

Shandong Provincial Institute of Dermatology and Venereology, Shandong Academy of Medical Sciences, Jinan, China; Shandong Provincial Hospital for Skin Diseases, Shandong University, Jinan, China; Shandong Provincial Key Lab for Dermatovenereology, Jinan, China; Shandong Provincial Medical Center for Dermatovenereology, Jinan, China; School of Medicine, Shandong University, Jinan, China; School of Medicine and Life Science, University of Jinan-Shandong Academy of Medical Sciences, Jinan, Shandong, China; National Clinical Key Project of Dermatology and Venereology, Jinan, China. Electronic address:

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http://dx.doi.org/10.1016/j.jid.2017.08.004DOI Listing
December 2017

Screening for TMEM230 mutations in young-onset Parkinson's disease.

Neurobiol Aging 2017 10 24;58:239.e9-239.e10. Epub 2017 Jun 24.

Neurology, Singapore General Hospital, Singapore; Neurology, National Neuroscience Institute of Singapore, Singapore; Duke NUS Graduate Medical School, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2017.06.011DOI Listing
October 2017

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Authors:
Tin Aung Mineo Ozaki Mei Chin Lee Ursula Schlötzer-Schrehardt Gudmar Thorleifsson Takanori Mizoguchi Robert P Igo Aravind Haripriya Susan E Williams Yury S Astakhov Andrew C Orr Kathryn P Burdon Satoko Nakano Kazuhiko Mori Khaled Abu-Amero Michael Hauser Zheng Li Gopalakrishnan Prakadeeswari Jessica N Cooke Bailey Alina Popa Cherecheanu Jae H Kang Sarah Nelson Ken Hayashi Shin-Ichi Manabe Shigeyasu Kazama Tomasz Zarnowski Kenji Inoue Murat Irkec Miguel Coca-Prados Kazuhisa Sugiyama Irma Järvelä Patricio Schlottmann S Fabian Lerner Hasnaa Lamari Yildirim Nilgün Mukharram Bikbov Ki Ho Park Soon Cheol Cha Kenji Yamashiro Juan C Zenteno Jost B Jonas Rajesh S Kumar Shamira A Perera 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 Wirostko Samuel Thomas Daniel Gaston Karen Bedard Wenda L Greer Zhenglin Yang Xueyi Chen 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 Mardin Panayiota Founti Anthi Chatzikyriakidou Theofanis Pappas Eleftherios Anastasopoulos Alexandros Lambropoulos Arkasubhra Ghosh Rohit Shetty Natalia Porporato Vijayan Saravanan Rengaraj Venkatesh Chandrashekaran Shivkumar Narendran Kalpana Sripriya Sarangapani Mozhgan R Kanavi Afsaneh Naderi Beni Shahin Yazdani Alireza Lashay Homa Naderifar Nassim Khatibi Antonio 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 O Olawoye Adeyinka O Ashaye Idakwo Ugbede Adeola Onakoya Nkiru Kizor-Akaraiwe Chaiwat Teekhasaenee Yanin Suwan Wasu Supakontanasan Suhanya Okeke Nkechi J Uche Ifeoma 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 Michael Coote Jonathan G Crowston Sergei Y Astakhov Eugeny L Akopov Anton Emelyanov Vera Vysochinskaya Gyulli Kazakbaeva Rinat Fayzrakhmanov Saleh A Al-Obeidan Ohoud Owaidhah Leyla Ali Aljasim Balram Chowbay Jia Nee Foo Raphael Q Soh Kar Seng Sim Zhicheng 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 Hip X Nguyn Giang T T Nguyn Trình V Nguyn Werner Zenz Alexander Binder Daniela S Klobassa Martin L Hibberd Sonia Davila Stefan Herms Markus M Nöthen Susanne Moebus Robyn M Rautenbach Ari Ziskind Trevor R Carmichael Michele Ramsay Lydia Álvarez Montserrat García Héctor González-Iglesias Pedro P Rodríguez-Calvo Luis Fernández-Vega Cueto Çilingir Oguz Nevbahar Tamcelik Eray Atalay Bilge Batu Dilek Aktas Burcu Kasım M Roy Wilson Anne L Coleman Yutao Liu Pratap Challa Leon Herndon Rachel W Kuchtey John Kuchtey Karen Curtin Craig J Chaya Alan Crandall Linda M Zangwill Tien Yin Wong Masakazu Nakano Shigeru Kinoshita Anneke I den Hollander Eija Vesti John H Fingert Richard K Lee Arthur J Sit Bradford J Shingleton Ningli Wang Daniele Cusi 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 Jonathan L Haines Unnur Thorsteinsdottir Fridbert Jonasson R Rand Allingham Dan Milea Robert Ritch Toshiaki Kubota Kei Tashiro Eranga N Vithana Shazia Micheal Fotis Topouzis Jamie E Craig Michael Dubina Periasamy Sundaresan Kari Stefansson Janey L Wiggs Francesca Pasutto Chiea Chuen Khor

Nat Genet 2017 07 29;49(7):993-1004. Epub 2017 May 29.

Singapore Eye Research Institute, Singapore.

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http://dx.doi.org/10.1038/ng.3875DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685441PMC
July 2017

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.

Authors:
Philip C Haycock Stephen Burgess Aayah Nounu Jie Zheng George N Okoli Jack Bowden Kaitlin Hazel Wade Nicholas J Timpson David M Evans Peter Willeit Abraham Aviv Tom R Gaunt Gibran Hemani Massimo Mangino Hayley Patricia Ellis Kathreena M Kurian Karen A Pooley Rosalind A Eeles Jeffrey E Lee Shenying Fang Wei V Chen Matthew H Law Lisa M Bowdler Mark M Iles Qiong Yang Bradford B Worrall Hugh Stephen Markus Rayjean J Hung Chris I Amos Amanda B Spurdle Deborah J Thompson Tracy A O'Mara Brian Wolpin Laufey Amundadottir Rachael Stolzenberg-Solomon Antonia Trichopoulou N Charlotte Onland-Moret Eiliv Lund Eric J Duell Federico Canzian Gianluca Severi Kim Overvad Marc J Gunter Rosario Tumino Ulrika Svenson Andre van Rij Annette F Baas Matthew J Bown Nilesh J Samani Femke N G van t'Hof Gerard Tromp Gregory T Jones Helena Kuivaniemi James R Elmore Mattias Johansson James Mckay Ghislaine Scelo Robert Carreras-Torres Valerie Gaborieau Paul Brennan Paige M Bracci Rachel E Neale Sara H Olson Steven Gallinger Donghui Li Gloria M Petersen Harvey A Risch Alison P Klein Jiali Han Christian C Abnet Neal D Freedman Philip R Taylor John M Maris Katja K Aben Lambertus A Kiemeney Sita H Vermeulen John K Wiencke Kyle M Walsh Margaret Wrensch Terri Rice Clare Turnbull Kevin Litchfield Lavinia Paternoster Marie Standl Gonçalo R Abecasis John Paul SanGiovanni Yong Li Vladan Mijatovic Yadav Sapkota Siew-Kee Low Krina T Zondervan Grant W Montgomery Dale R Nyholt David A van Heel Karen Hunt Dan E Arking Foram N Ashar Nona Sotoodehnia Daniel Woo Jonathan Rosand Mary E Comeau W Mark Brown Edwin K Silverman John E Hokanson Michael H Cho Jennie Hui Manuel A Ferreira Philip J Thompson Alanna C Morrison Janine F Felix Nicholas L Smith Angela M Christiano Lynn Petukhova Regina C Betz Xing Fan Xuejun Zhang Caihong Zhu Carl D Langefeld Susan D Thompson Feijie Wang Xu Lin David A Schwartz Tasha Fingerlin Jerome I Rotter Mary Frances Cotch Richard A Jensen Matthias Munz Henrik Dommisch Arne S Schaefer Fang Han Hanna M Ollila Ryan P Hillary Omar Albagha Stuart H Ralston Chenjie Zeng Wei Zheng Xiao-Ou Shu Andre Reis Steffen Uebe Ulrike Hüffmeier Yoshiya Kawamura Takeshi Otowa Tsukasa Sasaki Martin Lloyd Hibberd Sonia Davila Gang Xie Katherine Siminovitch Jin-Xin Bei Yi-Xin Zeng Asta Försti Bowang Chen Stefano Landi Andre Franke Annegret Fischer David Ellinghaus Carlos Flores Imre Noth Shwu-Fan Ma Jia Nee Foo Jianjun Liu Jong-Won Kim David G Cox Olivier Delattre Olivier Mirabeau Christine F Skibola Clara S Tang Merce Garcia-Barcelo Kai-Ping Chang Wen-Hui Su Yu-Sun Chang Nicholas G Martin Scott Gordon Tracey D Wade Chaeyoung Lee Michiaki Kubo Pei-Chieng Cha Yusuke Nakamura Daniel Levy Masayuki Kimura Shih-Jen Hwang Steven Hunt Tim Spector Nicole Soranzo Ani W Manichaikul R Graham Barr Bratati Kahali Elizabeth Speliotes Laura M Yerges-Armstrong Ching-Yu Cheng Jost B Jonas Tien Yin Wong Isabella Fogh Kuang Lin John F Powell Kenneth Rice Caroline L Relton Richard M Martin George Davey Smith

JAMA Oncol 2017 May;3(5):636-651

MRC Integrative Epidemiology Unit, University of Bristol, Bristol, England2School of Social and Community Medicine, University of Bristol, Bristol, England.

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http://dx.doi.org/10.1001/jamaoncol.2016.5945DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638008PMC
May 2017

Possible Interaction Between Cigarette Smoking and HLA-DRB1 Variation in the Risk of Follicular Lymphoma.

Am J Epidemiol 2017 04;185(8):681-687

Department of Medicine Solna, Clinical Epidemiology Unit, Karolinska Institutet, Stockholm, Sweden.

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http://dx.doi.org/10.1093/aje/kww118DOI Listing
April 2017

Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia.

Mov Disord 2016 12 27;31(12):1924-1925. Epub 2016 Oct 27.

Duke-NUS Graduate Medical School, Singapore.

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http://dx.doi.org/10.1002/mds.26822DOI Listing
December 2016

A Synonymous Variant in IL10RA Affects RNA Splicing in Paediatric Patients with Refractory Inflammatory Bowel Disease.

J Crohns Colitis 2016 Nov 13;10(11):1366-1371. Epub 2016 May 13.

Department of Biochemistry and Molecular Biology, University of Ulsan College of Medicine, Seoul, Korea

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http://dx.doi.org/10.1093/ecco-jcc/jjw102DOI Listing
November 2016

An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma.

Hum Mol Genet 2016 08 19;25(16):3626-3634. Epub 2016 Jul 19.

Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine

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http://dx.doi.org/10.1093/hmg/ddw200DOI Listing
August 2016

Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction.

Sci Transl Med 2016 06;8(345):345ra88

Department of Nephrology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510080, China. Key Laboratory of Nephrology, Ministry of Health and Guangdong Province, Guangzhou, Guangdong 510080, China.

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http://stm.sciencemag.org/content/scitransmed/8/345/345ra88.
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http://dx.doi.org/10.1126/scitranslmed.aaf2106DOI Listing
June 2016

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.

Authors:
Chiea Chuen Khor Tan Do Hongyan Jia Masakazu Nakano Ronnie George Khaled Abu-Amero Roopam Duvesh Li Jia Chen Zheng Li Monisha E Nongpiur Shamira A Perera Chunyan Qiao Hon-Tym Wong Hiroshi Sakai Mônica Barbosa de Melo Mei-Chin Lee Anita S Chan Yaakub Azhany Thi Lam Huong Dao Yoko Ikeda Rodolfo A Perez-Grossmann Tomasz Zarnowski Alexander C Day Jost B Jonas Pancy O S Tam Tuan Anh Tran Humaira Ayub Farah Akhtar Shazia Micheal Paul T K Chew Leyla A Aljasim Tanuj Dada Tam Thi Luu Mona S Awadalla Naris Kitnarong Boonsong Wanichwecharungruang Yee Yee Aung Jelinar Mohamed-Noor Saravanan Vijayan Sripriya Sarangapani Rahat Husain Aliza Jap Mani Baskaran David Goh Daniel H Su Huaizhou Wang Vernon K Yong Leonard W Yip Tuyet Bach Trinh Manchima Makornwattana Thanh Thu Nguyen Edgar U Leuenberger Ki-Ho Park Widya Artini Wiyogo Rajesh S Kumar Celso Tello Yasuo Kurimoto Suman S Thapa Kessara Pathanapitoon John F Salmon Yong Ho Sohn Antonio Fea Mineo Ozaki Jimmy S M Lai Visanee Tantisevi Chaw Chaw Khaing Takanori Mizoguchi Satoko Nakano Chan-Yun Kim Guangxian Tang Sujie Fan Renyi Wu Hailin Meng Thi Thuy Giang Nguyen Tien Dat Tran Morio Ueno Jose Maria Martinez Norlina Ramli Yin Mon Aung Rigo Daniel Reyes Stephen A Vernon Seng Kheong Fang Zhicheng Xie Xiao Yin Chen Jia Nee Foo Kar Seng Sim Tina T Wong Desmond T Quek Rengaraj Venkatesh Srinivasan Kavitha Subbiah R Krishnadas Nagaswamy Soumittra Balekudaru Shantha Boon-Ang Lim Jeanne Ogle José P C de Vasconcellos Vital P Costa Ricardo Y Abe Bruno B de Souza Chelvin C Sng Maria C Aquino Ewa Kosior-Jarecka Guillermo Barreto Fong Vania Castro Tamanaja Ricardo Fujita Yuzhen Jiang Naushin Waseem Sancy Low Huan Nguyen Pham Sami Al-Shahwan E Randy Craven Muhammad Imran Khan Rrima Dada Kuldeep Mohanty Muneeb A Faiq Alex W Hewitt Kathryn P Burdon Eng Hui Gan Anuwat Prutthipongsit Thipnapa Patthanathamrongkasem Mary Ann T Catacutan Irene R Felarca Chona S Liao Emma Rusmayani Vira Wardhana Istiantoro Giulia Consolandi Giulia Pignata Carlo Lavia Prin Rojanapongpun Lerprat Mangkornkanokpong Sunee Chansangpetch Jonathan C H Chan Bonnie N K Choy Jennifer W H Shum Hlaing May Than Khin Thida Oo Aye Thi Han Victor H Yong Xiao-Yu Ng Shuang Ru Goh Yaan Fun Chong Martin L Hibberd Mark Seielstad Eileen Png Sarah J Dunstan Nguyen Van Vinh Chau Jinxin Bei Yi Xin Zeng Abhilasha Karkey Buddha Basnyat Francesca Pasutto Daniela Paoli Paolo Frezzotti Jie Jin Wang Paul Mitchell John H Fingert R Rand Allingham Michael A Hauser Soon Thye Lim Soo Hong Chew Richard P Ebstein Anavaj Sakuntabhai Kyu Hyung Park Jeeyun Ahn Greet Boland Harm Snippe Richard Stead Raquel Quino Su Nyunt Zaw Urszula Lukasik Rohit Shetty Mimiwati Zahari Hyoung Won Bae Nay Lin Oo Toshiaki Kubota Anita Manassakorn Wing Lau Ho Laura Dallorto Young Hoon Hwang Christine A Kiire Masako Kuroda Zeiras Eka Djamal Jovell Ian M Peregrino Arkasubhra Ghosh Jin Wook Jeoung Tung S Hoan Nuttamon Srisamran Thayanithi Sandragasu Saw Htoo Set Vi Huyen Doan Shomi S Bhattacharya Ching-Lin Ho Donald T Tan Ramanjit Sihota Seng-Chee Loon Kazuhiko Mori Shigeru Kinoshita Anneke I den Hollander Raheel Qamar Ya-Xing Wang Yik Y Teo E-Shyong Tai Curt Hartleben-Matkin David Lozano-Giral Seang Mei Saw Ching-Yu Cheng Juan C Zenteno Chi Pui Pang Huong T T Bui Owen Hee Jamie E Craig Deepak P Edward Michiko Yonahara Jamil Miguel Neto Maria L Guevara-Fujita Liang Xu Robert Ritch Ahmad Tajudin Liza-Sharmini Tien Y Wong Saleh Al-Obeidan Nhu Hon Do Periasamy Sundaresan Clement C Tham Paul J Foster Lingam Vijaya Kei Tashiro Eranga N Vithana Ningli Wang Tin Aung

Nat Genet 2016 May 4;48(5):556-62. Epub 2016 Apr 4.

Singapore Eye Research Institute, Singapore National Eye Centre and Eye ACP, Duke-National University of Singapore, Singapore.

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http://www.nature.com/articles/ng.3540
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http://dx.doi.org/10.1038/ng.3540DOI Listing
May 2016

Targeted next-generation sequencing to diagnose disorders of HDL cholesterol.

J Lipid Res 2015 Oct 8;56(10):1993-2001. Epub 2015 Aug 8.

Translational Laboratory in Genetic Medicine, Agency for Science Technology and Research (ASTAR) and National University of Singapore, Singapore Healthy Heart Program Prevention Clinic, St. Paul's Hospital, Vancouver, Canada Centre for Heart Lung Innovation, University of British Columbia, Vancouver, Canada Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore Departments of Medicine University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1194/jlr.P058891DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4583092PMC
October 2015

Mitochondrial serine protease HTRA2 gene mutation in Asians with coexistent essential tremor and Parkinson disease.

Neurogenetics 2015 Jul 20;16(3):241-2. Epub 2015 Mar 20.

Department of Neurology, National Neuroscience Institute, Level 6, Academia, 20 College Road, Singapore, 169856, Singapore.

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http://dx.doi.org/10.1007/s10048-015-0443-3DOI Listing
July 2015

A common variant near TGFBR3 is associated with primary open angle glaucoma.

Authors:
Zheng Li R Rand Allingham Masakazu Nakano Liyun Jia Yuhong Chen Yoko Ikeda Baskaran Mani Li-Jia Chen Changwon Kee David F Garway-Heath Sarangapani Sripriya Nobuo Fuse Khaled K Abu-Amero Chukai Huang Prasanthi Namburi Kathryn Burdon Shamira A Perera Puya Gharahkhani Ying Lin Morio Ueno Mineo Ozaki Takanori Mizoguchi Subbiah Ramasamy Krishnadas Essam A Osman Mei Chin Lee Anita S Y Chan Liza-Sharmini A Tajudin Tan Do Aurelien Goncalves Pascal Reynier Hong Zhang Rupert Bourne David Goh David Broadway Rahat Husain Anil K Negi Daniel H Su Ching-Lin Ho Augusto Azuara Blanco Christopher K S Leung Tina T Wong Azhany Yakub Yutao Liu Monisha E Nongpiur Jong Chul Han Do Nhu Hon Balekudaru Shantha Bowen Zhao Jinghong Sang NiHong Zhang Ryuichi Sato Kengo Yoshii Songhomita Panda-Jonas Allison E Ashley Koch Leon W Herndon Sayoko E Moroi Pratap Challa Jia Nee Foo Jin-Xin Bei Yi-Xin Zeng Cameron P Simmons Tran Nguyen Bich Chau Philomenadin Ferdinamarie Sharmila Merwyn Chew Blanche Lim Pansy O S Tam Elaine Chua Xiao Yu Ng Victor H K Yong Yaan Fun Chong Wee Yang Meah Saravanan Vijayan Sohn Seongsoo Wang Xu Yik Ying Teo Jessica N Cooke Bailey Jae H Kang Jonathan L Haines Ching Yu Cheng Seang-Mei Saw E-Shyong Tai Julia E Richards Robert Ritch Douglas E Gaasterland Louis R Pasquale Jianjun Liu Jost B Jonas Dan Milea Ronnie George Saleh A Al-Obeidan Kazuhiko Mori Stuart Macgregor Alex W Hewitt Christopher A Girkin Mingzhi Zhang Periasamy Sundaresan Lingam Vijaya David A Mackey Tien Yin Wong Jamie E Craig Xinghuai Sun Shigeru Kinoshita Janey L Wiggs Chiea-Chuen Khor Zhenglin Yang Chi Pui Pang Ningli Wang Michael A Hauser Kei Tashiro Tin Aung Eranga N Vithana

Hum Mol Genet 2015 Jul 10;24(13):3880-92. Epub 2015 Apr 10.

Singapore Eye Research Institute, Department of Ophthalmology, Yong Loo Lin School of Medicine, Duke-NUS Graduate Medical School, Singapore, Singapore,

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http://dx.doi.org/10.1093/hmg/ddv128DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459396PMC
July 2015

Nonsynonymous variants in MC1R are rare in Chinese Parkinson disease cases.

Ann Neurol 2015 Jul 25;78(1):152-3. Epub 2015 May 25.

Department of Neurology, Singapore General Hospital, National Neuroscience Institute, Singapore.

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http://dx.doi.org/10.1002/ana.24419DOI Listing
July 2015

CHCHD2 and Parkinson's disease.

Lancet Neurol 2015 Jul;14(7):681-2

Department of Neurology, Singapore General Hospital, National Neuroscience Institute, Singapore 169108, Singapore; Duke-National University of Singapore Graduate Medical School, Singapore. Electronic address:

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http://dx.doi.org/10.1016/S1474-4422(15)00098-8DOI Listing
July 2015

Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Authors:
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 Yury S Astakhov Khaled K Abu-Amero Juan C Zenteno Yildirim Nilgün Tomasz Zarnowski Mohammad Pakravan Leen Abu Safieh Liyun Jia Ya Xing Wang Susan Williams Daniela Paoli Patricio G Schlottmann Lulin Huang Kar Seng Sim Jia Nee Foo Masakazu Nakano Yoko Ikeda Rajesh S 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 Paul Leo Yaz Yetkin Çilingir Oğuz Mozhgan Rezaei Kanavi Afsaneh Naderi Beni Shahin Yazdani Evgeny L Akopov 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 Paul Mitchell Jie Jin Wang Ari Ziskind Trevor Carmichael Rangappa Ramakrishnan Kalpana Narendran Rangaraj Venkatesh Saravanan Vijayan Peiquan Zhao Xueyi Chen Dalia Guadarrama-Vallejo Ching Yu Cheng Shamira A Perera Rahat Husain Su-Ling Ho Ulrich-Christoph Welge-Luessen Christian 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 Michae Coote Bowen Zhao Jinghong Sang Nihong Zhang Qisheng You Vera Vysochinskaya Panayiota Founti Anthoula Chatzikyriakidou Alexandros Lambropoulos Eleftherios Anastasopoulos Anne L Coleman M Roy Wilson Douglas J Rhee Jae Hee 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 Dubina Jamie E Craig Nagahisa Yoshimura Periasamy Sundaresan Simon W M John Robert Ritch Michael A Hauser Chiea-Chuen Khor

Nat Genet 2015 Jun;47(6):689

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http://dx.doi.org/10.1038/ng0615-689cDOI Listing
June 2015

GWAS reveal novel IgA nephropathy risk loci.

Oncotarget 2015 Jun;6(18):15738-9

Department of Nephrology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599228PMC
http://dx.doi.org/10.18632/oncotarget.4632DOI Listing
June 2015

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.

Authors:
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 Yury S Astakhov Khaled K Abu-Amero Juan C Zenteno Yildirim Nilgün Tomasz Zarnowski Mohammad Pakravan Leen Abu Safieh Liyun Jia Ya Xing Wang Susan Williams Daniela Paoli Patricio G Schlottmann Lulin Huang Kar Seng Sim Jia Nee Foo Masakazu Nakano Yoko Ikeda Rajesh S 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 Paul Leo Yaz Yetkin Çilingir Oğuz Mozhgan Rezaei Kanavi Afsaneh Nederi Beni Shahin Yazdani Evgeny L Akopov 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 Paul Mitchell Jie Jin Wang Ari Ziskind Trevor Carmichael Rangappa Ramakrishnan Kalpana Narendran Rangaraj Venkatesh Saravanan Vijayan Peiquan Zhao Xueyi Chen Dalia Guadarrama-Vallejo Ching Yu Cheng Shamira A Perera Rahat Husain Su-Ling Ho Ulrich-Christoph Welge-Luessen Christian 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 Eleftherios Anastasopoulos Anne L Coleman M Roy Wilson Douglas J Rhee Jae Hee 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 Dubina Jamie E Craig Nagahisa Yoshimura Periasamy Sundaresan Simon W M John Robert Ritch Michael A Hauser Chiea-Chuen Khor

Nat Genet 2015 Apr 23;47(4):387-92. Epub 2015 Feb 23.

1] Singapore Eye Research Institute, Singapore. [2] Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore. [3] Division of Human Genetics, Genome Institute of Singapore, Singapore.

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http://dx.doi.org/10.1038/ng.3226DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605818PMC
April 2015

Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.

Nat Commun 2015 Apr 23;6:6916. Epub 2015 Apr 23.

1] State Key Laboratory Incubation Base of Dermatology, Ministry of National Science and Technology, Anhui Medical University, Hefei, Anhui 230032, China [2] Key Lab of Dermatology (Anhui Medical University), Ministry of Education, Hefei, Anhui 230032, China [3] Collaborative Innovation Center for Complex and Severe Skin Diseases, Anhui Medical University, Hefei, Anhui 230032, China [4] Department of Human Genetics, Genome Institute of Singapore, A*STAR, Singapore 138672, Singapore [5] Saw Swee Hock School of Public Health, National University of Singapore, National University Health System, Singapore, 138672, Singapore [6] School of Life Sciences, Anhui Medical University, Hefei, Anhui 230032, China.

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http://dx.doi.org/10.1038/ncomms7916DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423213PMC
April 2015

Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nat Commun 2015 Mar 30;6:6817. Epub 2015 Mar 30.

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http://dx.doi.org/10.1038/ncomms7817DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400603PMC
March 2015

New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nat Commun 2015 Jan 28;6:6063. Epub 2015 Jan 28.

1] Singapore Eye Research Institute, Singapore 169856, Singapore [2] Division of Human Genetics, Genome Institute of Singapore, Singapore 138672, Singapore [3] Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore 117549, Singapore.

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http://dx.doi.org/10.1038/ncomms7063DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317498PMC
January 2015

Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.

PLoS One 2014 3;9(2):e87250. Epub 2014 Feb 3.

Shandong Provincial Institute of Dermatology and Venereology, Provincial Academy of Medical Science, Jinan, Shandong, China ; Shandong Provincial Hospital for Skin Diseases, Shandong University, Jinan, Shandong, China ; Shandong Provincial Key Lab for Dermatovenereology, Jinan, Shandong, China ; Shandong Provincial Medical Center for Dermatovenereology, Jinan, Shandong, China ; Shandong Clinical College, Anhui Medical University, Jinan, Shandong, China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0087250PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911924PMC
December 2014

Variation at HLA-DRB1 is associated with resistance to enteric fever.

Nat Genet 2014 Dec 10;46(12):1333-6. Epub 2014 Nov 10.

1] Genome Institute of Singapore, Singapore. [2] Singapore Eye Research Institute, Singapore. [3] Saw Swee Hock School of Public Health, National University of Singapore, Singapore. [4] Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore. [5] Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

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http://dx.doi.org/10.1038/ng.3143DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099079PMC
December 2014

Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data.

BMC Proc 2014 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S29. Epub 2014 Jun 17.

Human Genetics, Genome Institute of Singapore, #02-01, Genome, 60 Biopolis Street, 138672, Republic of Singapore.

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http://dx.doi.org/10.1186/1753-6561-8-S1-S29DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143774PMC
December 2014

Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region.

Authors:
Christine F Skibola Sonja I Berndt Joseph Vijai Lucia Conde Zhaoming Wang Meredith Yeager Paul I W de Bakker Brenda M Birmann Claire M Vajdic Jia-Nee Foo Paige M Bracci Roel C H Vermeulen Susan L Slager Silvia de Sanjose Sophia S Wang Martha S Linet Gilles Salles Qing Lan Gianluca Severi Henrik Hjalgrim Tracy Lightfoot Mads Melbye Jian Gu Hervé Ghesquières Brian K Link Lindsay M Morton Elizabeth A Holly Alex Smith Lesley F Tinker Lauren R Teras Anne Kricker Nikolaus Becker Mark P Purdue John J Spinelli Yawei Zhang Graham G Giles Paolo Vineis Alain Monnereau Kimberly A Bertrand Demetrius Albanes Anne Zeleniuch-Jacquotte Attilio Gabbas Charles C Chung Laurie Burdett Amy Hutchinson Charles Lawrence Rebecca Montalvan Liming Liang Jinyan Huang Baoshan Ma Jianjun Liu Hans-Olov Adami Bengt Glimelius Yuanqing Ye Grzegorz S Nowakowski Ahmet Dogan Carrie A Thompson Thomas M Habermann Anne J Novak Mark Liebow Thomas E Witzig George J Weiner Maryjean Schenk Patricia Hartge Anneclaire J De Roos Wendy Cozen Degui Zhi Nicholas K Akers Jacques Riby Martyn T Smith Mortimer Lacher Danylo J Villano Ann Maria Eve Roman Eleanor Kane Rebecca D Jackson Kari E North W Ryan Diver Jenny Turner Bruce K Armstrong Yolanda Benavente Paolo Boffetta Paul Brennan Lenka Foretova Marc Maynadie Anthony Staines James McKay Angela R Brooks-Wilson Tongzhang Zheng Theodore R Holford Saioa Chamosa Rudolph Kaaks Rachel S Kelly Bodil Ohlsson Ruth C Travis Elisabete Weiderpass Jacqueline Clavel Edward Giovannucci Peter Kraft Jarmo Virtamo Patrizio Mazza Pierluigi Cocco Maria Grazia Ennas Brian C H Chiu Joseph F Fraumeni Alexandra Nieters Kenneth Offit Xifeng Wu James R Cerhan Karin E Smedby Stephen J Chanock Nathaniel Rothman

Am J Hum Genet 2014 Oct;95(4):462-71

Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.ajhg.2014.09.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4185120PMC
October 2014

Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.

Hum Mol Genet 2014 Jul 23;23(14):3891-7. Epub 2014 Feb 23.

Human Genetics, Genome Institute of Singapore, A*STAR, Singapore Saw Swee Hock School of Public Health, National University of Singapore, National University Health System, Singapore

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http://dx.doi.org/10.1093/hmg/ddu086DOI Listing
July 2014

Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing.

PLoS Genet 2014 May 15;10(5):e1004377. Epub 2014 May 15.

Saw Swee Hock School of Public Health, National University of Singapore, Singapore; NUS Graduate School for Integrative Science and Engineering, National University of Singapore, Singapore; Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore; Life Sciences Institute, National University of Singapore, Singapore; Department of Statistics and Applied Probability, National University of Singapore, Singapore.

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http://dx.doi.org/10.1371/journal.pgen.1004377DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022468PMC
May 2014

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls.

Neurobiol Aging 2014 Apr 12;35(4):935.e1-2. Epub 2013 Oct 12.

Departments of Neurology, Singapore General Hospital, National Neuroscience Institute, 169108, Singapore; Duke-NUS Graduate Medical School, Singapore. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.09.018DOI Listing
April 2014

Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease.

Neurobiol Aging 2013 Dec 18;34(12):2890.e13-5. Epub 2013 Jul 18.

Human Genetics, Genome Institute of Singapore, A*STAR, Singapore.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.06.010DOI Listing
December 2013

Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseases.

Neurobiol Aging 2013 Oct 4;34(10):2441.e7-8. Epub 2013 May 4.

Department of Neurology, Singapore General Hospital, Singapore; National Neuroscience Institute, Singapore, Singapore.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.04.012DOI Listing
October 2013

Identification of a novel risk variant in the FUS gene in essential tremor.

Neurology 2013 Aug 3;81(6):541-4. Epub 2013 Jul 3.

Human Genetics, Genome Institute of Singapore, A*STAR, Singapore.

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http://dx.doi.org/10.1212/WNL.0b013e31829e700cDOI Listing
August 2013

Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspective.

Hum Genet 2013 Jul 23;132(7):721-34. Epub 2013 Mar 23.

Human Genetics, Genome Institute of Singapore, A STAR, 60 Biopolis Street, Genome #02-01, Singapore 138672, Singapore.

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http://link.springer.com/10.1007/s00439-013-1287-2
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http://dx.doi.org/10.1007/s00439-013-1287-2DOI Listing
July 2013

Analysis of EIF4G1 in Parkinson's disease among Asians.

Neurobiol Aging 2013 Apr 23;34(4):1311.e5-6. Epub 2012 Oct 23.

Departments of Neurology and Clinical Research, Singapore General Hospital, National Neuroscience Institute, Singapore.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.09.003DOI Listing
April 2013

SLC1A2 variant associated with essential tremor but not Parkinson disease in Chinese subjects.

Neurology 2013 Apr 17;80(17):1618-9. Epub 2013 Apr 17.

Department of Neurology, Singapore General Hospital, Singapore.

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http://dx.doi.org/10.1212/WNL.0b013e31828f1903DOI Listing
April 2013

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.

Nat Genet 2013 Feb 6;45(2):155-63. Epub 2013 Jan 6.

Queensland Institute of Medical Research, Statistical Genetics, Herston, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1038/ng.2506DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720123PMC
February 2013

A meta-analysis of genome-wide association studies of follicular lymphoma.

BMC Genomics 2012 Oct 1;13:516. Epub 2012 Oct 1.

School of Public Health, Division of Environmental Health Sciences, University of California, Berkeley, 94720, USA.

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http://dx.doi.org/10.1186/1471-2164-13-516DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3534234PMC
October 2012

Whole-genome and whole-exome sequencing in neurological diseases.

Nat Rev Neurol 2012 Sep 31;8(9):508-17. Epub 2012 Jul 31.

Human Genetics, Genome Institute of Singapore, A*STAR, 60 Biopolis Street, Genome #02-01, Singapore 138672.

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http://dx.doi.org/10.1038/nrneurol.2012.148DOI Listing
September 2012

Apolipoprotein C3 gene variants in nonalcoholic fatty liver disease.

N Engl J Med 2010 Mar;362(12):1082-9

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.

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http://dx.doi.org/10.1056/NEJMoa0907295DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976042PMC
March 2010