Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: BMF[original query] |
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Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.
PLoS genetics 2011 Apr 7 (4): e1002025. Zhai Guangju, Teumer Alexander, Stolk Lisette, Perry John R B, Vandenput Liesbeth, Coviello Andrea D, Koster Annemarie, Bell Jordana T, Bhasin Shalender, Eriksson Joel, Eriksson Anna, Ernst Florian, Ferrucci Luigi, Frayling Timothy M, Glass Daniel, Grundberg Elin, Haring Robin, Hedman Asa K, Hofman Albert, Kiel Douglas P, Kroemer Heyo K, Liu Yongmei, Lunetta Kathryn L, Maggio Marcello, Lorentzon Mattias, Mangino Massimo, Melzer David, Miljkovic Iva, , Nica Alexandra, Penninx Brenda W J H, Vasan Ramachandran S, Rivadeneira Fernando, Small Kerrin S, Soranzo Nicole, Uitterlinden André G, Völzke Henry, Wilson Scott G, Xi Li, Zhuang Wei Vivian, Harris Tamara B, Murabito Joanne M, Ohlsson Claes, Murray Anna, de Jong Frank H, Spector Tim D, Wallaschofski Hen |
Impact of immunogenetic polymorphisms in bone marrow failure syndromes. Mini reviews in medicinal chemistry 2011 Jun 11 (6): 544-52. Serio B, Selleri C, Maciejewski J |
FANCA and FANCG are the major Fanconi anemia genes in the Korean population. Clinical genetics 2013 Sep 84 (3): 271-5. Park J, Chung N-G, Chae H, Kim M, Lee S, Kim Y, Lee J-W, Cho B, Jeong D C, Park I |
Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients. Blood 2013 Oct 122 (18): 3206-9. Hira Asuka, Yabe Hiromasa, Yoshida Kenichi, Okuno Yusuke, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Miyano Satoru, Nakamura Jun, Kojima Seiji, Ogawa Seishi, Matsuo Keitaro, Takata Minoru, Yabe Miha |
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Nature genetics 2013 Aug 45 (8): 868-76. Berndt Sonja I, Skibola Christine F, Joseph Vijai, Camp Nicola J, Nieters Alexandra, Wang Zhaoming, Cozen Wendy, Monnereau Alain, Wang Sophia S, Kelly Rachel S, Lan Qing, Teras Lauren R, Chatterjee Nilanjan, Chung Charles C, Yeager Meredith, Brooks-Wilson Angela R, Hartge Patricia, Purdue Mark P, Birmann Brenda M, Armstrong Bruce K, Cocco Pierluigi, Zhang Yawei, Severi Gianluca, Zeleniuch-Jacquotte Anne, Lawrence Charles, Burdette Laurie, Yuenger Jeffrey, Hutchinson Amy, Jacobs Kevin B, Call Timothy G, Shanafelt Tait D, Novak Anne J, Kay Neil E, Liebow Mark, Wang Alice H, Smedby Karin E, Adami Hans-Olov, Melbye Mads, Glimelius Bengt, Chang Ellen T, Glenn Martha, Curtin Karen, Cannon-Albright Lisa A, Jones Brandt, Diver W Ryan, Link Brian K, Weiner George J, Conde Lucia, Bracci Paige M, Riby Jacques, Holly Elizabeth A, Smith Martyn T, Jackson Rebecca D, Tinker Lesley F, Benavente Yolanda, Becker Nikolaus, Boffetta Paolo, Brennan Paul, Foretova Lenka, Maynadie Marc, McKay James, Staines Anthony, Rabe Kari G, Achenbach Sara J, Vachon Celine M, Goldin Lynn R, Strom Sara S, Lanasa Mark C, Spector Logan G, Leis Jose F, Cunningham Julie M, Weinberg J Brice, Morrison Vicki A, Caporaso Neil E, Norman Aaron D, Linet Martha S, De Roos Anneclaire J, Morton Lindsay M, Severson Richard K, Riboli Elio, Vineis Paolo, Kaaks Rudolph, Trichopoulos Dimitrios, Masala Giovanna, Weiderpass Elisabete, Chirlaque María-Dolores, Vermeulen Roel C H, Travis Ruth C, Giles Graham G, Albanes Demetrius, Virtamo Jarmo, Weinstein Stephanie, Clavel Jacqueline, Zheng Tongzhang, Holford Theodore R, Offit Kenneth, Zelenetz Andrew, Klein Robert J, Spinelli John J, Bertrand Kimberly A, Laden Francine, Giovannucci Edward, Kraft Peter, Kricker Anne, Turner Jenny, Vajdic Claire M, Ennas Maria Grazia, Ferri Giovanni M, Miligi Lucia, Liang Liming, Sampson Joshua, Crouch Simon, Park Ju-Hyun, North Kari E, Cox Angela, Snowden John A, Wright Josh, Carracedo Angel, Lopez-Otin Carlos, Bea Silvia, Salaverria Itziar, Martin-Garcia David, Campo Elias, Fraumeni Joseph F, de Sanjose Silvia, Hjalgrim Henrik, Cerhan James R, Chanock Stephen J, Rothman Nathaniel, Slager Susan |
Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan. International journal of hematology 2015 Sep . Yamaguchi Hiroki, Sakaguchi Hirotoshi, Yoshida Kenichi, Yabe Miharu, Yabe Hiromasa, Okuno Yusuke, Muramatsu Hideki, Takahashi Yoshiyuki, Yui Shunsuke, Shiraishi Yuichi, Chiba Kenichi, Tanaka Hiroko, Miyano Satoru, Inokuchi Koiti, Ito Etsuro, Ogawa Seishi, Kojima Sei |
Genetic Predisposition to Chronic Lymphocytic Leukemia Is Mediated by a BMF Super-Enhancer Polymorphism. Cell reports 2016 Aug . Kandaswamy Radhika, Sava Georgina P, Speedy Helen E, Beà Sílvia, Martín-Subero José I, Studd James B, Migliorini Gabriele, Law Philip J, Puente Xose S, Martín-García David, Salaverria Itziar, Gutiérrez-Abril Jesús, López-Otín Carlos, Catovsky Daniel, Allan James M, Campo Elías, Houlston Richard |
Five endometrial cancer risk loci identified through genome-wide association analysis.
Nature genetics 2016 May . Cheng Timothy H T, Thompson Deborah J, O'Mara Tracy A, Painter Jodie N, Glubb Dylan M, Flach Susanne, Lewis Annabelle, French Juliet D, Freeman-Mills Luke, Church David, Gorman Maggie, Martin Lynn, , Hodgson Shirley, Webb Penelope M, , Attia John, Holliday Elizabeth G, McEvoy Mark, Scott Rodney J, Henders Anjali K, Martin Nicholas G, Montgomery Grant W, Nyholt Dale R, Ahmed Shahana, Healey Catherine S, Shah Mitul, Dennis Joe, Fasching Peter A, Beckmann Matthias W, Hein Alexander, Ekici Arif B, Hall Per, Czene Kamila, Darabi Hatef, Li Jingmei, Dörk Thilo, Dürst Matthias, Hillemanns Peter, Runnebaum Ingo, Amant Frederic, Schrauwen Stefanie, Zhao Hui, Lambrechts Diether, Depreeuw Jeroen, Dowdy Sean C, Goode Ellen L, Fridley Brooke L, Winham Stacey J, Njølstad Tormund S, Salvesen Helga B, Trovik Jone, Werner Henrica M J, Ashton Katie, Otton Geoffrey, Proietto Tony, Liu Tao, Mints Miriam, Tham Emma, , , Li Mulin Jun, Yip Shun H, Wang Junwen, Bolla Manjeet K, Michailidou Kyriaki, Wang Qin, Tyrer Jonathan P, Dunlop Malcolm, Houlston Richard, Palles Claire, Hopper John L, , Peto Julian, Swerdlow Anthony J, Burwinkel Barbara, Brenner Hermann, Meindl Alfons, Brauch Hiltrud, Lindblom Annika, Chang-Claude Jenny, Couch Fergus J, Giles Graham G, Kristensen Vessela N, Cox Angela, Cunningham Julie M, Pharoah Paul D P, Dunning Alison M, Edwards Stacey L, Easton Douglas F, Tomlinson Ian, Spurdle Amanda |
Sex hormones are negatively associated with vertebral bone marrow fat. Bone 2017 12 108 20-24. Mistry Swaroop D, Woods Gina N, Sigurdsson Sigurdur, Ewing Susan K, Hue Trisha F, Eiriksdottir Gudny, Xu Kaipin, Hilton Joan F, Kado Deborah M, Gudnason Vilmundur, Harris Tamara B, Rosen Clifford J, Lang Thomas F, Li Xiaojuan, Schwartz Ann |
Fanconi Anemia germline variants as susceptibility factors in aplastic anemia, MDS and AML. Oncotarget 2018 Jan 9 (2): 2050-2057. Przychodzen Bartlomiej, Makishima Hideki, Sekeres Mikkael A, Balasubramanian Suresh Kumar, Thota Swapna, Patel Bhumika J, Clemente Michael, Hirsch Cassandra, Dienes Brittney, Maciejewski Jaroslaw |
Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia. Annals of hematology 2019 Feb 98 (2): 271-280. Yabe Miharu, Koike Takashi, Ohtsubo Keisuke, Imai Eri, Morimoto Tsuyoshi, Takakura Hiromitsu, Koh Katsuyoshi, Yoshida Kenichi, Ogawa Seishi, Ito Etsuro, Okuno Yusuke, Muramatsu Hideki, Kojima Seiji, Matsuo Keitaro, Mori Minako, Hira Asuka, Takata Minoru, Yabe Hiroma |
Heterozygous RTEL1 variants in bone marrow failure and myeloid neoplasms. Blood advances 2018 Jan 2 (1): 36-48. Marsh Judith C W, Gutierrez-Rodrigues Fernanda, Cooper James, Jiang Jie, Gandhi Shreyans, Kajigaya Sachiko, Feng Xingmin, Ibanez Maria Del Pilar F, Donaires Flávia S, Lopes da Silva João P, Li Zejuan, Das Soma, Ibanez Maria, Smith Alexander E, Lea Nicholas, Best Steven, Ireland Robin, Kulasekararaj Austin G, McLornan Donal P, Pagliuca Anthony, Callebaut Isabelle, Young Neal S, Calado Rodrigo T, Townsley Danielle M, Mufti Ghulam |
Comparison of Outcomes of Myeloablative Allogeneic Stem Cell Transplantation for Pediatric Patients with Bone Marrow Failure, Myelodysplastic Syndrome and Acute Myeloid Leukemia with and without Germline GATA2 Mutations. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2020 2 26 (6): 1124-1130. Hofmann Inga, Avagyan Serine, Stetson Alyssa, Guo Dongjing, Al-Sayegh Hasan, London Wendy B, Lehmann Lesl |
Decoding Bone Marrow Fibrosis in Myelodysplastic Syndromes. Clinical lymphoma, myeloma & leukemia 2020 2 20 (5): 324-328. Melody Megan, Al Ali Najla, Zhang Ling, Ramadan Hanadi, Padron Eric, Sallman David, Sweet Kendra, Lancet Jeffrey, List Alan, Bennett John M, Komrokji Ra |
Pediatric bone marrow failure: Clinical, hematological and targeted next generation sequencing data. Blood cells, molecules & diseases 2020 11 87 102510. Chhabra Prashant, Bhatia Prateek, Singh Minu, Bansal Deepak, Jain Richa, Varma Neelam, Trehan Ami |
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2). The Journal of allergy and clinical immunology 2020 1 145 (6): 1664-1672.e10. Lee Pui Y, Kellner Erinn S, Huang Yuelong, Furutani Elissa, Huang Zhengping, Bainter Wayne, Alosaimi Mohammed F, Stafstrom Kelsey, Platt Craig D, Stauber Tali, Raz Somech, Tirosh Irit, Weiss Aaron, Jordan Michael B, Krupski Christa, Eleftheriou Despina, Brogan Paul, Sobh Ali, Baz Zeina, Lefranc Gerard, Irani Carla, Kilic Sara S, El-Owaidy Rasha, Lokeshwar M R, Pimpale Pallavi, Khubchandani Raju, Chambers Eugene P, Chou Janet, Geha Raif S, Nigrovic Peter A, Zhou Qi |
Pulmonary fibrosis in dyskeratosis congenita: a case report with a PRISMA-compliant systematic review. BMC pulmonary medicine 2021 9 21 (1): 279. Wang Ping, Xu Zuoj |
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
Graft-versus-host disease after liver transplantation is associated with bone marrow failure, hemophagocytosis, and DNMT3A mutations. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2021 5 21 (12): 3894-3906. Newell Laura F, Dunlap Jennifer, Gatter Ken, Bagby Grover C, Press Richard D, Cook Rachel J, Fletcher Luke, Leonard Jessica T, Leong Kelli M, Bubalo Joseph S, Olyaei Ali, Deloughery Thomas G, Maziarz Richard T, Maynard Erin, Orloff Susan L, Enestvedt C Kristi |
Disease progression and clinical outcomes in telomere biology disorders. Blood 2021 12 139 (12): 1807-1819. Niewisch Marena R, Giri Neelam, McReynolds Lisa J, Alsaggaf Rotana, Bhala Sonia, Alter Blanche P, Savage Sharon |
The similarity of class II HLA genotypes defines patterns of autoreactivity in idiopathic bone marrow failure disorders. Blood 2021 11 138 (26): 2781-2798. Pagliuca Simona, Gurnari Carmelo, Awada Hassan, Kishtagari Ashwin, Kongkiatkamon Sunisa, Terkawi Laila, Zawit Misam, Guan Yihong, LaFramboise Thomas, Jha Babal K, Patel Bhumika J, Hamilton Betty K, Majhail Navneet S, Lundgren Sofie, Mustjoki Satu, Saunthararajah Yogen, Visconte Valeria, Chan Timothy A, Yang Chao-Yie, Lenz Tobias L, Maciejewski Jaroslaw |
Predictive Value of miR-146a rs2431697 Polymorphism to Myelofibrosis Progression in Patients with Myeloproliferative Neoplasm. Asian Pacific journal of cancer prevention : APJCP 2021 Nov 22 (11): 3585-3589. Aref Salah, Atia Doaa, Al Tantawy Ahmed, Al Boghdady Mohamed, Gouda En |
Breast Cancer Prognosis Prediction and Immune Pathway Molecular Analysis Based on Mitochondria-Related Genes. Genetics research 2022 2022 2249909. Luo Weixu, Han Yuanshan, Li Xin, Liu Zhuo, Meng Pan, Wang Yuho |
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort. Haematologica 2022 4 108 (1): 69-82. Altintas Burak, Giri Neelam, McReynolds Lisa J, Best Ana, Alter Blanche |
Tumor stromal nicotinamide N-methyltransferase overexpression as a prognostic biomarker for poor clinical outcome in early-stage colorectal cancer. Scientific reports 2022 02 12 (1): 2767. Ogawa Makiko, Tanaka Atsushi, Namba Kei, Shia Jinru, Wang Julia Y, Roehrl Michael H |
Significance of hereditary gene alterations for the pathogenesis of adult bone marrow failure versus myeloid neoplasia. Leukemia 2022 Oct . Kubota Yasuo, Zawit Misam, Durrani Jibran, Shen Wenyi, Bahaj Waled, Kewan Tariq, Ponvilawan Ben, Mori Minako, Meggendorfer Manja, Gurnari Carmelo, LaFramboise Thomas, Feurstein Simone, Sekeres Mikkael A, Visconte Valeria, Godley Lucy A, Haferlach Torsten, Maciejewski Jaroslaw |
The Clinical Picture of the ERCC6L2 Disease - from Bone Marrow Failure to Acute Leukemia. Blood 2023 3 . Hakkarainen Marja, Kaaja Ilse, Douglas Suvi P M, Vulliamy Thomas J, Dokal Inderjeet, Soulier Jean, Larcher Lise, Peffault de Latour Régis, Leblanc Thierry M, Sicre de Fontbrune Flore, Siitonen Timo, Lohi Olli, Hellström-Lindberg Eva, Barbany Gisela, Tesi Bianca, Shimamura Akiko, Beier Fabian, Jackson Sharon Rosalie, Kuperman Amir, Falik Zaccai Tzipora C, Tamary Hannah, Mecucci Cristina, Capolsini Ilaria, Jahnukainen Kirsi, Salmenniemi Urpu, Niinimäki Riitta, Varilo Teppo, Kilpivaara Outi, Wartiovaara-Kautto Ul |
A Cohort Study on Deficiency of ADA2 from China. Journal of clinical immunology 2023 2 . Li Guo-Min, Han Xu, Wu Ye, Wang Wei, Tang Hong-Xia, Lu Mei-Ping, Tang Xue-Mei, Lin Yi, Deng Fan, Yang Jun, Wang Xin-Ning, Liu Cong-Cong, Zheng Wen-Jie, Wu Bing-Bing, Zhou Fang, Luo Hong, Zhang Liang, Liu Hai-Mei, Guan Wan-Zhen, Wang Shi-Hao, Tao Pan-Feng, Jin Tai-Jie, Fang Ran, Wu Yuan, Zhang Jie, Zhang Yao, Zhang Tian-Nan, Yin Wei, Guo Li, Tang Wen-Jing, Chang Hong, Zhang Qiu-Ye, Li Xiao-Zhong, Li Jian-Guo, Zhou Zhi-Xuan, Yang Si-Rui, Yang Kang-Kang, Xu Hong, Song Hong-Mei, Deuitch Natalie T, Lee Pui Y, Zhou Qing, Sun |
Incorporating mutations and bone marrow fibrosis into the revised international prognostic scoring system in myelodysplastic syndromes. Leukemia & lymphoma 2023 10 1-9. Youshan Zhao, Juan Guo, Sida Zhao, Roujia Wang, Dong Wu, Chunkang Cha |
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Nature genetics 2023 3 55 (3): 423-436. Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak B?a?ej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel C, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode Kathyrn M, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, S?omka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szy??o Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, , , , , , Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Tim, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez-Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina |
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