HuGE Literature Finder
Records 1-30
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Association of Glaucoma Risk Genes with Retinal Nerve Fiber Layer in a Multi-ethnic Asian Population: The Singapore Epidemiology of Eye Diseases Study.
Investigative ophthalmology & visual science 2020 Aug 61 (10): 37. Chai Xiaoran, Low Kok Yao, Tham Yih Chung, Chee Miao Li, Thakur Sahil, Zhang Liang, Tan Nicholas Y, Khor Chiea Chuen, Aung Tin, Wong Tien Yin, Cheng Ching- |
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Exploring new genetic variants within COL5A1 intron 4-exon 5 region and TGF-ß family with risk of anterior cruciate ligament ruptures.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2020 Jan . Laguette Mary-Jessica N, Barrow Kelly, Firfirey Firzana, Dlamini Senanile, Saunders Colleen J, Dandara Collet, Gamieldien Junaid, Collins Malcolm, September Alison |
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Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.
The journal of sexual medicine 2019 Oct . Cintho Ozahata Mina, Page Grier P, Guo Yuelong, Ferreira João Eduardo, Dinardo Carla Luana, Carneiro-Proietti Anna Bárbara F, Loureiro Paula, Mota Rosimere Afonso, Rodrigues Daniela O W, Belisario André Rolim, Maximo Claudia, Flor-Park Miriam V, Custer Brian, Kelly Shannon, Sabino Ester Cerdeira, |
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Genes associated with testicular germ cell tumors and testicular dysgenesis in patients with testicular microlithiasis.
Asian journal of andrology 2018 Jul . Dantsev Ilya S, Ivkin Evgeniy V, Tryakin Aleksey A, Godlevski Dmitriy N, Latyshev Oleg Yu, Rudenko Victoriya V, Mikhaylenko Dmitry S, Chernykh Vyacheslav B, Volodko Elena A, Okulov Aleksey B, Loran Oleg B, Nemtsova Marina |
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Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype.
BioMed research international 2018 2018 8386123. Sticchi Elena, De Cario Rosina, Magi Alberto, Giglio Sabrina, Provenzano Aldesia, Nistri Stefano, Pepe Guglielmina, Giusti Bet |
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Lack of Association of rs1192415 in
Frontiers in genetics 2018 9 488. Chen Yuhong, Qiu Chen, Qian Shaohong, Chen Junyi, Chen Xueli, Wang Li, Sun Xinghu |
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Journal of medical genetics 2017 May 54 (5): 313-323. Noordam Raymond, Sitlani Colleen M, Avery Christy L, Stewart James D, Gogarten Stephanie M, Wiggins Kerri L, Trompet Stella, Warren Helen R, Sun Fangui, Evans Daniel S, Li Xiaohui, Li Jin, Smith Albert V, Bis Joshua C, Brody Jennifer A, Busch Evan L, Caulfield Mark J, Chen Yii-Der I, Cummings Steven R, Cupples L Adrienne, Duan Qing, Franco Oscar H, Méndez-Giráldez Rául, Harris Tamara B, Heckbert Susan R, van Heemst Diana, Hofman Albert, Floyd James S, Kors Jan A, Launer Lenore J, Li Yun, Li-Gao Ruifang, Lange Leslie A, Lin Henry J, de Mutsert Renée, Napier Melanie D, Newton-Cheh Christopher, Poulter Neil, Reiner Alexander P, Rice Kenneth M, Roach Jeffrey, Rodriguez Carlos J, Rosendaal Frits R, Sattar Naveed, Sever Peter, Seyerle Amanda A, Slagboom P Eline, Soliman Elsayed Z, Sotoodehnia Nona, Stott David J, Stürmer Til, Taylor Kent D, Thornton Timothy A, Uitterlinden André G, Wilhelmsen Kirk C, Wilson James G, Gudnason Vilmundur, Jukema J Wouter, Laurie Cathy C, Liu Yongmei, Mook-Kanamori Dennis O, Munroe Patricia B, Rotter Jerome I, Vasan Ramachandran S, Psaty Bruce M, Stricker Bruno H, Whitsel Eric |
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A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population.
Investigative ophthalmology & visual science 2017 Jan 58 (1): 87-95. Nannini Drew R, Torres Mina, Chen Yii-Der I, Taylor Kent D, Rotter Jerome I, Varma Rohit, Gao Xiao |
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Genetic Variants in CD44 and MAT1A Confer Susceptibility to Acute Skin Reaction in Breast Cancer Patients Undergoing Radiation Therapy.
International journal of radiation oncology, biology, physics 2016 Sep . Mumbrekar Kamalesh Dattaram, Bola Sadashiva Satish Rao, Kabekkodu Shama Prasada, Fernandes Donald Jerard, Vadhiraja Bejadi Manjunath, Suga Tomo, Shoji Yoshimi, Nakayama Fumiaki, Imai Takashi, Satyamoorthy Kapaet |
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Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.
Annals of hematology 2016 Aug . Belisário André Rolim, Sales Rahyssa Rodrigues, Toledo Nayara Evelin, Muniz Maristela Braga de Sousa Rodrigues, Velloso-Rodrigues Cibele, Silva Célia Maria, Viana Marcos Bora |
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A genome-wide approach to screen for genetic variants in broilers (Gallus gallus) with divergent feed conversion ratio.
Molecular genetics and genomics : MGG 2016 May . Shah Tejas M, Patel Namrata V, Patel Anand B, Upadhyay Maulik R, Mohapatra Amitbikram, Singh Krishna M, Deshpande Sunil D, Joshi Chaitanya |
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A Genetic Variant in TGFBR3-CDC7 Is Associated with Visual Field Progression in Primary Open-Angle Glaucoma Patients from Singapore.
Ophthalmology 2015 Sep . Trikha Sameer, Saffari Ehsan, Nongpiur Monisha, Baskaran Mani, Ho Henrietta, Li Zheng, Tan Peng-Yi, Allen John, Khor Chiea-Chuen, Perera Shamira A, Cheng Ching-Yu, Aung Tin, Vithana Eran |
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Surrogate molecular markers for IGHV mutational status in chronic lymphocytic leukemia for predicting time to first treatment.
Leukemia research 2015 Aug 39 (8): 840-5. Morabito Fortunato, Cutrona Giovanna, Mosca Laura, D'Anca Marianna, Matis Serena, Gentile Massimo, Vigna Ernesto, Colombo Monica, Recchia Anna Grazia, Bossio Sabrina, De Stefano Laura, Maura Francesco, Manzoni Martina, Ilariucci Fiorella, Consoli Ugo, Vincelli Iolanda, Musolino Caterina, Cortelezzi Agostino, Molica Stefano, Ferrarini Manlio, Neri Antoni |
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A common variant near TGFBR3 is associated with primary open angle glaucoma.
Human molecular genetics 2015 Jul 24 (13): 3880-92. Li Zheng, Allingham R Rand, Nakano Masakazu, Jia Liyun, Chen Yuhong, Ikeda Yoko, Mani Baskaran, Chen Li-Jia, Kee Changwon, Garway-Heath David F, Sripriya Sarangapani, Fuse Nobuo, Abu-Amero Khaled K, Huang Chukai, Namburi Prasanthi, Burdon Kathryn, Perera Shamira A, Gharahkhani Puya, Lin Ying, Ueno Morio, Ozaki Mineo, Mizoguchi Takanori, Krishnadas Subbiah Ramasamy, Osman Essam A, Lee Mei Chin, Chan Anita S Y, Tajudin Liza-Sharmini A, Do Tan, Goncalves Aurelien, Reynier Pascal, Zhang Hong, Bourne Rupert, Goh David, Broadway David, Husain Rahat, Negi Anil K, Su Daniel H, Ho Ching-Lin, Blanco Augusto Azuara, Leung Christopher K S, Wong Tina T, Yakub Azhany, Liu Yutao, Nongpiur Monisha E, Han Jong Chul, Hon Do Nhu, Shantha Balekudaru, Zhao Bowen, Sang Jinghong, Zhang NiHong, Sato Ryuichi, Yoshii Kengo, Panda-Jonas Songhomita, Ashley Koch Allison E, Herndon Leon W, Moroi Sayoko E, Challa Pratap, Foo Jia Nee, Bei Jin-Xin, Zeng Yi-Xin, Simmons Cameron P, Bich Chau Tran Nguyen, Sharmila Philomenadin Ferdinamarie, Chew Merwyn, Lim Blanche, Tam Pansy O S, Chua Elaine, Ng Xiao Yu, Yong Victor H K, Chong Yaan Fun, Meah Wee Yang, Vijayan Saravanan, Seongsoo Sohn, Xu Wang, Teo Yik Ying, Cooke Bailey Jessica N, Kang Jae H, Haines Jonathan L, Cheng Ching Yu, Saw Seang-Mei, Tai E-Shyong, , , Richards Julia E, Ritch Robert, Gaasterland Douglas E, Pasquale Louis R, Liu Jianjun, Jonas Jost B, Milea Dan, George Ronnie, Al-Obeidan Saleh A, Mori Kazuhiko, Macgregor Stuart, Hewitt Alex W, Girkin Christopher A, Zhang Mingzhi, Sundaresan Periasamy, Vijaya Lingam, Mackey David A, Wong Tien Yin, Craig Jamie E, Sun Xinghuai, Kinoshita Shigeru, Wiggs Janey L, Khor Chiea-Chuen, Yang Zhenglin, Pang Chi Pui, Wang Ningli, Hauser Michael A, Tashiro Kei, Aung Tin, Vithana Eranga |
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Association analysis of TGFBR3 gene with Behçet's disease and idiopathic intermediate uveitis in a Caucasian population.
The British journal of ophthalmology 2015 May 99 (5): 696-9. Barry Robert J, Alsalem Jawaher A, Faassen Juliet, Murray Philip I, Curnow S John, Wallace Graham |
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Large-scale evaluation of common variation in regulatory T cell-related genes and ovarian cancer outcome.
Cancer immunology research 2014 Apr 2 (4): 332-40. Charbonneau Bridget, Moysich Kirsten B, Kalli Kimberly R, Oberg Ann L, Vierkant Robert A, Fogarty Zachary C, Block Matthew S, Maurer Matthew J, Goergen Krista M, Fridley Brooke L, Cunningham Julie M, Rider David N, Preston Claudia, Hartmann Lynn C, Lawrenson Kate, Wang Chen, Tyrer Jonathan, Song Honglin, deFazio Anna, Johnatty Sharon E, Doherty Jennifer A, Phelan Catherine M, Sellers Thomas A, Ramirez Starr M, Vitonis Allison F, Terry Kathryn L, Van Den Berg David, Pike Malcolm C, Wu Anna H, Berchuck Andrew, Gentry-Maharaj Aleksandra, Ramus Susan J, Diergaarde Brenda, Shen Howard, Jensen Allan, Menkiszak Janusz, Cybulski Cezary, Lubi?ski Jan, Ziogas Argyrios, Rothstein Joseph H, McGuire Valerie, Sieh Weiva, Lester Jenny, Walsh Christine, Vergote Ignace, Lambrechts Sandrina, Despierre Evelyn, Garcia-Closas Montserrat, Yang Hannah, Brinton Louise A, Spiewankiewicz Beata, Rzepecka Iwona K, Dansonka-Mieszkowska Agnieszka, Seibold Petra, Rudolph Anja, Paddock Lisa E, Orlow Irene, Lundvall Lene, Olson Sara H, Hogdall Claus K, Schwaab Ira, du Bois Andreas, Harter Philipp, Flanagan James M, Brown Robert, Paul James, Ekici Arif B, Beckmann Matthias W, Hein Alexander, Eccles Diana, Lurie Galina, Hays Laura E, Bean Yukie T, Pejovic Tanja, Goodman Marc T, Campbell Ian, Fasching Peter A, Konecny Gottfried, Kaye Stanley B, Heitz Florian, Hogdall Estrid, Bandera Elisa V, Chang-Claude Jenny, Kupryjanczyk Jolanta, Wentzensen Nicolas, Lambrechts Diether, Karlan Beth Y, Whittemore Alice S, Culver Hoda Anton, Gronwald Jacek, Levine Douglas A, Kjaer Susanne K, Menon Usha, Schildkraut Joellen M, Pearce Celeste Leigh, Cramer Daniel W, Rossing Mary Anne, Chenevix-Trench Georgia, , , Pharoah Paul D P, Gayther Simon A, Ness Roberta B, Odunsi Kunle, Sucheston Lara E, Knutson Keith L, Goode Ellen |
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The influence of genetic ancestry and ethnicity on breast cancer survival associated with genetic variation in the TGF-?-signaling pathway: The Breast Cancer Health Disparities Study.
Cancer causes & control : CCC 2014 Mar 25 (3): 293-307. Slattery Martha L, Lundgreen Abbie, Stern Marianna C, Hines Lisa, Wolff Roger K, Giuliano Anna R, Baumgartner Kathy B, John Esther |
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Associations between genetic variants in the TGF-? signaling pathway and breast cancer risk among Hispanic and non-Hispanic white women.
Breast cancer research and treatment 2013 Sep 141 (2): 287-97. Boone Stephanie D, Baumgartner Kathy B, Baumgartner Richard N, Connor Avonne E, Pinkston Christina M, John Esther M, Hines Lisa M, Stern Mariana C, Giuliano Anna R, Torres-Mejia Gabriela, Brock Guy N, Groves Frank D, Kerber Richard A, Wolff Roger K, Slattery Martha |
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The genetics of Behçet's disease in a Chinese population.
Frontiers of medicine 2012 Nov . Hou S, Kijlstra A, Yang P |
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Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.
Current eye research 2012 Apr 37 (4): 312-7. Chen Yuanyuan, Yang Peizeng, Li Fuzhen, Hou Shengping, Jiang Zhengxuan, Shu Qinmeng, Kijlstra Ai |
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A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation.
Journal of medical genetics 2012 Jan 49 (1): 58-65. Dalgaard Marlene D, Weinhold Nils, Edsgärd Daniel, Silver Jeremy D, Pers Tune H, Nielsen John E, Jørgensen Niels, Juul Anders, Gerds Thomas A, Giwercman Aleksander, Giwercman Yvonne L, Cohn-Cedermark Gabriella, Virtanen Helena E, Toppari Jorma, Daugaard Gedske, Jensen Thomas S, Brunak Søren, Rajpert-De Meyts Ewa, Skakkebæk Niels E, Leffers Henrik, Gupta Ramne |
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Haplotype and mutation analysis of the TGFBR3 gene in Chinese women with idiopathic premature ovarian failure.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2012 Jan 28 (1): 63-7. Qin Chun-rong, Chen Shi-ling, Yao Ji-long, Li Tao, Wu Wei-qi |
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Independent validation of genes and polymorphisms reported to be associated with radiation toxicity: a prospective analysis study.
The Lancet. Oncology 2012 Jan 13 (1): 65-77. Barnett Gillian C, Coles Charlotte E, Elliott Rebecca M, Baynes Caroline, Luccarini Craig, Conroy Don, Wilkinson Jennifer S, Tyrer Jonathan, Misra Vivek, Platte Radka, Gulliford Sarah L, Sydes Matthew R, Hall Emma, Bentzen Søren M, Dearnaley David P, Burnet Neil G, Pharoah Paul D P, Dunning Alison M, West Catharine M |
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Polymorphisms in the potential functional regions of the TGF-? 1 and TGF-? receptor genes and disease susceptibility in HBV-related hepatocellular carcinoma patients.
Molecular carcinogenesis 2012 Jan . Xin Z, Zhang W, Xu A, Zhang L, Yan T, Li Z, Wu X, Zhu X, Ma J, Li K, Li H, Liu Y |
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CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies.
PloS one 2012 7 (6): e39278. Cao Dan, Jiao Xiaodong, Liu Xing, Hennis Anselm, Leske M Cristina, Nemesure Barbara, Hejtmancik J Fieldi |
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TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome.
Journal of negative results in biomedicine 2012 11 (1): 9. Singh Krishna K, Schmidtke Joerg, Keyser Britta, Arslan-Kirchner Mi |
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Identification of novel missense mutations of the TGFBR3 gene in Chinese women with premature ovarian failure.
Reproductive biomedicine online 2011 Dec 23 (6): 697-703. Qin Chun-rong, Chen Shi-ling, Yao Ji-long, Wu Wei-qing, Xie Jian-she |
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Development of a multicomponent prediction model for acute esophagitis in lung cancer patients receiving chemoradiotherapy.
International journal of radiation oncology, biology, physics 2011 Oct 81 (2): 537-44. De Ruyck Kim, Sabbe Nick, Oberije Cary, Vandecasteele Katrien, Thas Olivier, De Ruysscher Dirk, Lambin Phillipe, Van Meerbeeck Jan, De Neve Wilfried, Thierens Hube |
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Common genetic variants associated with open-angle glaucoma.
Human molecular genetics 2011 Jun 20 (12): 2464-71. Ramdas Wishal D, van Koolwijk Leonieke M E, Lemij Hans G, Pasutto Francesca, Cree Angela J, Thorleifsson Gudmar, Janssen Sarah F, Jacoline Ten Brink, Amin Najaf, Rivadeneira Fernando, Wolfs Roger C W, Walters G Bragi, Jonasson Fridbert, Weisschuh Nicole, Mardin Christian Y, Gibson Jane, Zegers Richard H C, Hofman Albert, de Jong Paulus T V M, Uitterlinden André G, Oostra Ben A, Thorsteinsdottir Unnur, Gramer Eugen, Welgen-Lüssen Ulrich C, Kirwan James F, Bergen Arthur A B, Reis André, Stefansson Kari, Lotery Andrew J, Vingerling Johannes R, Jansonius Nomdo M, Klaver Caroline C W, van Duijn Cornelia |
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Genetic predictors for stroke in children with sickle cell anemia.
Blood 2011 Jun 117 (24): 6681-4. Flanagan Jonathan M, Frohlich Denise M, Howard Thad A, Schultz William H, Driscoll Catherine, Nagasubramanian Ramamoorthy, Mortier Nicole A, Kimble Amy C, Aygun Banu, Adams Robert J, Helms Ronald W, Ware Russell |
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Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area.
Human molecular genetics 2011 May 20 (9): 1864-72. Khor Chiea Chuen, Ramdas Wishal D, Vithana Eranga N, Cornes Belinda K, Sim Xueling, Tay Wan-Ting, Saw Seang-Mei, Zheng Yingfeng, Lavanya Raghavan, Wu Renyi, Wang Jie Jin, Mitchell Paul, Uitterlinden André G, Rivadeneira Fernando, Teo Yik-Ying, Chia Kee-Seng, Seielstad Mark, Hibberd Martin, Vingerling Johannes R, Klaver Caroline C W, Jansonius Nomdo M, Tai E-Shyong, Wong Tien-Yin, van Duijn Cornelia M, Aung T |
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Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2011 Apr 22 (4): 1079-90. Zmuda J M, Yerges-Armstrong L M, Moffett S P, Klei L, Kammerer C M, Roeder K, Cauley J A, Kuipers A, Ensrud K E, Nestlerode C S, Hoffman A R, Lewis C E, Lang T F, Barrett-Connor E, Ferrell R E, Orwoll E S, |
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A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study.
BMC medical genetics 2011 12 (1): 19. Roshandel Delnaz, Thomson Wendy, Pye Stephen R, Boonen Steven, Borghs Herman, Vanderschueren Dirk, Huhtaniemi Ilpo T, Adams Judith E, Ward Kate A, Bartfai Gyorgy, Casanueva Felipe, Finn Joseph D, Forti Gianni, Giwercman Aleksander, Han Thang S, Kula Krzysztof, Lean Michael E, Pendleton Neil, Punab Margus, Silman Alan J, Wu Frederick C, Holliday Kate L, O'Neill Terence W, |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.
Genome medicine 2011 3 (1): 3. Wang Joanne H, Pappas Derek, De Jager Philip L, Pelletier Daniel, de Bakker Paul Iw, Kappos Ludwig, Polman Chris H, , Chibnik Lori B, Hafler David A, Matthews Paul M, Hauser Stephen L, Baranzini Sergio E, Oksenberg Jorge |
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TGFBR3 polymorphisms and its haplotypes associated with chronic hepatitis B virus infection and age of hepatocellular carcinoma occurrence.
Digestive diseases (Basel, Switzerland) 2011 29 (3): 278-83. Kim Jeong-Hyun, Yu Su Jong, Park Byung-Lae, Cheong Hyun Sub, Pasaje Charisse Flerida A, Bae Joon Seol, Lee Hyo-Suk, Shin Hyoung Doo, Kim Yoon J |
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SNPs in genes coding for ROS metabolism and signalling in association with docetaxel clearance.
The pharmacogenomics journal 2010 Dec 10 (6): 513-23. Edvardsen H, Brunsvig P F, Solvang H, Tsalenko A, Andersen A, Syvanen A-C, Yakhini Z, Børresen-Dale A-L, Olsen H, Aamdal S, Kristensen V |
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A large-scale candidate gene association study of age at menarche and age at natural menopause.
Human genetics 2010 Nov 128 (5): 515-27. He Chunyan, Kraft Peter, Chasman Daniel I, Buring Julie E, Chen Constance, Hankinson Susan E, Paré Guillaume, Chanock Stephen, Ridker Paul M, Hunter David |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Interferon gamma receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection.
Gut 2010 Aug 59 (8): 1120-6. Nalpas Bertrand, Lavialle-Meziani Roubila, Plancoulaine Sabine, Jouanguy Emmanuelle, Nalpas Antoine, Munteanu Mona, Charlotte Frederic, Ranque Brigitte, Patin Etienne, Heath Simon, Fontaine Hélène, Vallet-Pichard Anaïs, Pontoire Dominique, Bourlière Marc, Casanova Jean-Laurent, Lathrop Mark, Bréchot Christian, Poynard Thierry, Matsuda Fumihiko, Pol Stanislas, Abel Laure |
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Association between genetic variations of the transforming growth factor ß receptor type III and asthma in a Korean population.
Experimental & molecular medicine 2010 Jun 42 (6): 420-7. Kim Hee-Kyoo, Jang Tae-Won, Jung Mann-Hong, Park Heung-Woo, Lee Jong-Eun, Shin Eun-Soon, Cho Sang-Heon, Min Kyung-Up, Kim You-You |
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L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms.
Nephron. Clinical practice 2010 115 (4): c237-43. Yokoyama Keitaro, Urashima Mitsuyoshi, Ohkido Ichiro, Kono Takashi, Yoshida Toyohiko, Muramatsu Masaaki, Niu Tianhua, Hosoya Tats |
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
PloS one 2010 5 (7): e11493. Jugessur Astanand, Shi Min, Gjessing Håkon Kristian, Lie Rolv Terje, Wilcox Allen James, Weinberg Clarice Ring, Christensen Kaare, Boyles Abee Lowman, Daack-Hirsch Sandra, Nguyen Truc Trung, Christiansen Lene, Lidral Andrew Carl, Murray Jeffrey Cla |
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Genetic determinants of immune-response to a polysaccharide vaccine for typhoid.
The HUGO journal 2009 Dec 3 (1-4): 1-4. Majumder PP, Staats HF, Sarkar-Roy N, Varma B, Ghosh T, Maiti S, Narayanasamy K, Whisnant CC, Stephenson JL, Wagener DK |
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High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 Dec 24 (12): 2039-49. Yerges Laura M, Klei Lambertus, Cauley Jane A, Roeder Kathryn, Kammerer Candace M, Moffett Susan P, Ensrud Kristine E, Nestlerode Cara S, Marshall Lynn M, Hoffman Andrew R, Lewis Cora, Lang Thomas F, Barrett-Connor Elizabeth, Ferrell Robert E, Orwoll Eric S, Zmuda Joseph M, |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Transforming growth factor-beta receptor-3 is associated with pulmonary emphysema.
American journal of respiratory cell and molecular biology 2009 Sep 41 (3): 324-31. Hersh Craig P, Hansel Nadia N, Barnes Kathleen C, Lomas David A, Pillai Sreekumar G, Coxson Harvey O, Mathias Rasika A, Rafaels Nicholas M, Wise Robert A, Connett John E, Klanderman Barbara J, Jacobson Francine L, Gill Ritu, Litonjua Augusto A, Sparrow David, Reilly John J, Silverman Edwin K, |
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Sequencing of TGF-beta pathway genes in familial cases of intracranial aneurysm.
Stroke; a journal of cerebral circulation 2009 May 40 (5): 1604-11. Santiago-Sim Teresa, Mathew-Joseph Sumy, Pannu Hariyadarshi, Milewicz Dianna M, Seidman Christine E, Seidman J G, Kim Dong |
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Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups.
American journal of human genetics 2009 Mar 84 (3): 388-98. Xiong Dong-Hai, Liu Xiao-Gang, Guo Yan-Fang, Tan Li-Jun, Wang Liang, Sha Bao-Yong, Tang Zi-Hui, Pan Feng, Yang Tie-Lin, Chen Xiang-Ding, Lei Shu-Feng, Yerges Laura M, Zhu Xue-Zen, Wheeler Victor W, Patrick Alan L, Bunker ClareAnn H, Guo Yan, Yan Han, Pei Yu-Fang, Zhang Yin-Pin, Levy Shawn, Papasian Christopher J, Xiao Peng, Lundberg Y Wang, Recker Robert R, Liu Yao-Zhong, Liu Yong-Jun, Zmuda Joseph M, Deng Hong-W |
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Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.
Genetics in medicine : official journal of the American College of Medical Genetics 2008 Sep 10 (9): 668-74. Vieira Alexandre R, McHenry Toby G, Daack-Hirsch Sandra, Murray Jeffrey C, Marazita Mary |
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Distinct association of genetic variations of vascular endothelial growth factor, transforming growth factor-beta, and fibroblast growth factor receptors with atopy and airway hyperresponsiveness.
Allergy 2008 Apr 63 (4): 447-53. Park H-K, Park H W, Jeon S G, Shin E-S, Gho Y S, Cho S-H, Kim Y-Y, Kim Y |
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Association of polymorphisms in complement component C3 gene with susceptibility to systemic lupus erythematosus.
Rheumatology (Oxford, England) 2008 Feb 47 (2): 158-64. Miyagawa H, Yamai M, Sakaguchi D, Kiyohara C, Tsukamoto H, Kimoto Y, Nakamura T, Lee J-H, Tsai C-Y, Chiang B-L, Shimoda T, Harada M, Tahira T, Hayashi K, Horiuchi |
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Genetic polymorphisms associated with priapism in sickle cell disease.
British journal of haematology 2007 May 137 (3): 262-7. Elliott Laine, Ashley-Koch Allison E, De Castro Laura, Jonassaint Jude, Price Jennifer, Ataga Kenneth I, Levesque Marc C, Brice Weinberg J, Eckman James R, Orringer Eugene P, Vance Jeffery M, Telen Marilyn |
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Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2006 Sep 43 (5): 593-8. Adewoye Adeboye H, Nolan Vikki G, Ma Qianli, Baldwin Clinton, Wyszynski Diego F, Farrell John J, Farrer Lindsay A, Steinberg Martin |
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Mutational analysis of the betaglycan gene-coding region in susceptibility for ovarian failure.
Human reproduction (Oxford, England) 2006 Aug 21 (8): 2041-6. Dixit H, Rao K L, Padmalatha V V, Kanakavalli M, Deenadayal M, Gupta N, Chakrabarty B N, Singh |
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Genetic susceptibility to keloid disease: transforming growth factor beta receptor gene polymorphisms are not associated with keloid disease.
Experimental dermatology 2004 Feb 13 (2): 120-4. Bayat A, Bock O, Mrowietz U, Ollier WE, Ferguson MW |
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Genetic susceptibility to Dupuytren's disease: transforming growth factor beta receptor (TGFbetaR) gene polymorphisms and Dupuytren's disease.
British journal of plastic surgery 2003 Jun 56 (4): 328-33. Bayat A, Stanley J K, Watson J S, Ferguson M W J, Ollier W E |
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Novel single nucleotide polymorphisms in the 3'-UTR of the TGFbetaRI and TGFbetaRIII genes.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 2002 Oct 29 (5): 445-6. Bayat A, Watson J S, Stanley J K, Ferguson M W J, Ollier W E |
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Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Molecular medicine (Cambridge, Mass.) 0 16 (7-8): 247-53. Rose Jed E, Behm Frédérique M, Drgon Tomas, Johnson Catherine, Uhl George |
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