Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and PROC[original query] |
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| Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium. Proceedings of the National Academy of Sciences of the United States of America 2002 1 99 (2): 827-31. Thompson Deborah, Szabo Csilla I, Mangion Jon, Oldenburg Rogier A, Odefrey Fabrice, Seal Sheila, Barfoot Rita, Kroeze-Jansema Karin, Teare Dawn, Rahman Nazneen, Renard Hélène, Mann Graham, Hopper John L, Buys Saundra S, Andrulis Irene L, Senie Ruby, Daly Mary B, West Dee, Ostrander Elaine A, Offit Ken, Peretz Tamar, Osorio Ana, Benitez J, Nathanson Katherine L, Sinilnikova Olga M, Olàh Edith, Bignon Yves-Jean, Ruiz Pablo, Badzioch Michael D, Vasen Hans F A, Futreal Andrew P, Phelan Catherine M, Narod Steven A, Lynch Henry T, Ponder Bruce A J, Eeles Ros A, Meijers-Heijboer Hanne, Stoppa-Lyonnet Dominique, Couch Fergus J, Eccles Diana M, Evans D Gareth, Chang-Claude Jenny, Lenoir Gilbert, Weber Barbara L, Devilee Peter, Easton Douglas F, Goldgar David E, Stratton Michael R, |
| Combined effects of thrombosis pathway gene variants predict cardiovascular events. PLoS genetics 2007 Jul 3 (7): e120. Auro Kirsi, Alanne Mervi, Kristiansson Kati, Silander Kaisa, Kuulasmaa Kari, Salomaa Veikko, Peltonen Leena, Perola Mark |
| PROC, PROCR and PROS1 polymorphisms, plasma anticoagulant phenotypes, and risk of cardiovascular disease and mortality in older adults: the Cardiovascular Health Study. Journal of thrombosis and haemostasis : JTH 2008 Oct 6 (10): 1625-32. Reiner A P, Carty C L, Jenny N S, Nievergelt C, Cushman M, Stearns-Kurosawa D J, Kurosawa S, Kuller L H, Lange L |
| DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America 2008 Aug 105 (33): 11869-74. Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart |
| Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease. Neurogenetics 2008 May 9 (2): 127-38. Lee Joseph H, Cheng Rong, Rogaeva Ekaterina, Meng Yan, Stern Yaakov, Santana Vincent, Lantigua Rafael, Medrano Martin, Jimenez-Velazquez Ivonne Z, Farrer Lindsay A, St George-Hyslop Peter, Mayeux Richa |
| Evidence that variation in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene is associated with psychosis in Alzheimer's disease. Neuroscience letters 2009 Sep 461 (1): 54-9. Sims R, Hollingworth P, Moskvina V, Dowzell K, O'Donovan M C, Powell J, Lovestone S, Brayne C, Rubinsztein D, Owen M J, Williams J, Abraham |
| [Polymorphic markers G(-455)A of gene FGB and C(-1654)T of gene PROC and genetic predisposition to unfavorable outcomes patients undergoing acute coronary syndrome]. Molekuliarnaia biologiia 0 44 (4): 613-9. Agapkina Iu V, Nikitin A G, Brovkin A N, Pushkov A A, Evdokimova M A, Kudriashova O Iu, Osmolovskaia V S, Minushkina L O, Kochkina M S, Selezneva N D, Dankovtseva E N, Chumakova O S, Baklanova T N, Talyzin P A, Reznichenko N E, Donetskaia O P, Tereshchenko S N, Krasil'nikova E S, Dzhaiani N A, Akatova E V, Glezer M G, Galiavich A S, Zakirova V B, Kaziolova N A, Timofeeva I V, Iagoda A V, Boeva O I, Katel'nitskaia L I, Khorolets E V, Shlyk S V, Volkova É G, Margarian M P, Guz' I O, Konstantinov V O, Timofeeva A N, Sidorenko B A, Zate?shchikiov D A, Nosikov V |
| Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study. Alzheimer's & dementia : the journal of the Alzheimer's Association 2014 May 10 (3): 366-71. Peterson David, Munger Caitlin, Crowley Jared, Corcoran Chris, Cruchaga Carlos, Goate Alison M, Norton Maria C, Green Robert C, Munger Ronald G, Breitner John C S, Welsh-Bohmer Kathleen A, Lyketsos Constantine, Tschanz Joann, Kauwe John S K, |
| [The preliminary research in paroxysmal nocturnal hemoglobinuria with thrombosis]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2016 Apr 37 (4): 318-23. Du Y L, Long Z B, Xie H Y, Zhuang J L, Han |
| Plasma levels of the anti-coagulation protein C and the risk of ischaemic heart disease. A Mendelian randomisation study. Thrombosis and haemostasis 2017 01 117 (2): 262-268. Schooling C Mary, Zhong |
| Polymorphisms of F2, PROC, PROZ, and F13A1 Genes are Associated With Recurrent Spontaneous Abortion in Chinese Han Women. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Jan 1076029617750487. Xu Zuying, Zhang Ying, Liu Wei, Liu Yunyun, Su Yezhou, Xing Qiong, He Xiaojin, Wei Zhaolian, Cao Yunxia, Xiang Huif |
| Targeted resequencing identifies genes with recurrent variation in cerebral palsy. NPJ genomic medicine 2019 4 27. van Eyk C L, Corbett M A, Frank M S B, Webber D L, Newman M, Berry J G, Harper K, Haines B P, McMichael G, Woenig J A, MacLennan A H, Gecz |
| Genetic Polymorphisms in Sepsis and Cardiovascular Disease: Do Similar Risk Genes Suggest Similar Drug Targets? Chest 2019 Jan . Nakada Taka-Aki, Takahashi Waka, Nakada Emiri, Shimada Tadanaga, Russell James A, Walley Keith |
| Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood 2020 May . Desch Karl C, Ozel Ayse B, Halvorsen Matt, Jacobi Paula M, Golden Krista, Underwood Mary, Germain Marine, Tregouet David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards J Brent, Williams Frances, Li Jun Z, Goldstein David, Ginsburg Dav |
| Olaparib in combination with pegylated liposomal doxorubicin for platinum-resistant ovarian cancer regardless of BRCA status: a GEICO phase II trial (ROLANDO study). ESMO open 2021 7 6 (4): 100212. Perez-Fidalgo J A, Cortés A, Guerra E, García Y, Iglesias M, Bohn Sarmiento U, Calvo García E, Manso Sánchez L, Santaballa A, Oaknin A, Redondo A, Rubio M J, González-Martín |
| Genetic Associations With Stable Warfarin Dose Requirements in Han Chinese Patients. Journal of cardiovascular pharmacology 2021 5 78 (1): e105-e111. Xu Qingqing, Zhang Suli, Wu Chaoneng, Xiong Yuyu, Niu Jiamin, Li Fengzhen, Zhu Jinhang, Shen Lu, Zhu Bin, Xing Qinghe, He Lin, Chen Luan, Li Mo, Li Hua, Ge Junbo, Qin Shengyi |
| [Genetic and Clinical Characteristics of A Family with Combined PROC and PROS1 Genetic Variants]. Zhongguo shi yan xue ye xue za zhi 2021 4 29 (2): 591-595. Wang Xing, Sheng Guang-Ying, Zhang Wei, Zhao Yun-Xiao, Xia Li-Jun, Jiang Mi |
| PARP Inhibitor in Platinum-Resistant Ovarian Cancer: Single-Center Real-World Experience. JCO global oncology 2021 4 7 506-511. Agarwal Amit, Baghmar Saphalta, Dodagoudar Chandragouda, Qureshi Suhail, Khurana Aseem, Vaibhav Vikas, Kumar Gure |
| Pamiparib Monotherapy for Patients with Germline BRCA1/2-Mutated Ovarian Cancer Previously Treated with at Least Two Lines of Chemotherapy: A Multicenter, Open-Label, Phase II Study. Clinical cancer research : an official journal of the American Association for Cancer Research 2021 11 28 (4): 653-661. Wu Xiaohua, Zhu Jianqing, Wang Jing, Lin Zhongqiu, Yin Rutie, Sun Wei, Zhou Qi, Zhang Songling, Wang Danbo, Shi Hong, Gao Yunong, Huang Yi, Li Guiling, Wang Xiuli, Cheng Ying, Lou Ge, Gao Qinglei, Wang Li, Du Xiuping, Pan Mei, Mu Xiyan, Li Li, Li Miao, Mu Song, Kong Beih |
| MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity. Journal of personalized medicine 2021 Nov 11 (11): . Cappadona Claudio, Paraboschi Elvezia Maria, Ziliotto Nicole, Bottaro Sandro, Rimoldi Valeria, Gerussi Alessio, Azimonti Andrea, Brenna Daniele, Brunati Andrea, Cameroni Charlotte, Campanaro Giovanni, Carloni Francesca, Cavadini Giacomo, Ciravegna Martina, Composto Antonio, Converso Giuseppe, Corbella Pierluigi, D'Eugenio Davide, Dal Rì Giovanna, Di Giorgio Sofia Maria, Grondelli Maria Chiara, Guerrera Lorenza, Laffoucriere Georges, Lando Beatrice, Lopedote Leandro, Maizza Benedetta, Marconi Elettra, Mariola Carlotta, Matronola Guia Margherita, Menga Luca Maria, Montorsi Giulia, Papatolo Antonio, Patti Riccardo, Profeta Lorenzo, Rebasti Vera, Smidili Alice, Tarchi Sofia Maria, Tartaglia Francesco Carlo, Tettamanzi Gaia, Tinelli Elena, Stuani Riccardo, Bolchini Cristiana, Pattini Linda, Invernizzi Pietro, Degenhardt Frauke, Franke Andre, Duga Stefano, Asselta Rosan |
| Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults: A Population-Based Cohort Study. Journal of the American Heart Association 2022 2 11 (4): e023018. Manderstedt Eric, Lind-Halldén Christina, Halldén Christer, Elf Johan, Svensson Peter J, Dahlbäck Björn, Engström Gunnar, Melander Olle, Baras Aris, Lotta Luca A, Zöller Bengt, |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
| The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood 2023 8 . Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria J Martin, James David Stephenson, Kalpana Paneerselvam, Slavé Petrovski, Pablo Porras, Peter N Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael Laffan, Willem H Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth Bruford, Dragana Vuckov |
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