Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: PRDM9[original query] |
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Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. Journal of assisted reproduction and genetics 0 25 (11-12): 553-7. Miyamoto Toshinobu, Koh Eitetsu, Sakugawa Naoko, Sato Hisashi, Hayashi Hiroaki, Namiki Mikio, Sengoku Kaz |
Single-nucleotide polymorphisms of the PRDM9 (MEISETZ) gene in patients with nonobstructive azoospermia. Journal of andrology 0 30 (4): 426-31. Irie Shinji, Tsujimura Akira, Miyagawa Yasushi, Ueda Tomohiro, Matsuoka Yasuhiro, Matsui Yasuhisa, Okuyama Akihiko, Nishimune Yoshitake, Tanaka Hiromit |
Fine-scale recombination rate differences between sexes, populations and individuals.
Nature 2010 Oct 467 (7319): 1099-103. Kong Augustine, Thorleifsson Gudmar, Gudbjartsson Daniel F, Masson Gisli, Sigurdsson Asgeir, Jonasdottir Aslaug, Walters G Bragi, Jonasdottir Adalbjorg, Gylfason Arnaldur, Kristinsson Kari Th, Gudjonsson Sigurjon A, Frigge Michael L, Helgason Agnar, Thorsteinsdottir Unnur, Stefansson Ka |
The landscape of recombination in African Americans.
Nature 2011 Jul 476 (7359): 170-5. Hinch Anjali G, Tandon Arti, Patterson Nick, Song Yunli, Rohland Nadin, Palmer Cameron D, Chen Gary K, Wang Kai, Buxbaum Sarah G, Akylbekova Ermeg L, Aldrich Melinda C, Ambrosone Christine B, Amos Christopher, Bandera Elisa V, Berndt Sonja I, Bernstein Leslie, Blot William J, Bock Cathryn H, Boerwinkle Eric, Cai Qiuyin, Caporaso Neil, Casey Graham, Cupples L Adrienne, Deming Sandra L, Diver W Ryan, Divers Jasmin, Fornage Myriam, Gillanders Elizabeth M, Glessner Joseph, Harris Curtis C, Hu Jennifer J, Ingles Sue A, Isaacs William, John Esther M, Kao W H Linda, Keating Brendan, Kittles Rick A, Kolonel Laurence N, Larkin Emma, Le Marchand Loic, McNeill Lorna H, Millikan Robert C, Murphy Adam, Musani Solomon, Neslund-Dudas Christine, Nyante Sarah, Papanicolaou George J, Press Michael F, Psaty Bruce M, Reiner Alex P, Rich Stephen S, Rodriguez-Gil Jorge L, Rotter Jerome I, Rybicki Benjamin A, Schwartz Ann G, Signorello Lisa B, Spitz Margaret, Strom Sara S, Thun Michael J, Tucker Margaret A, Wang Zhaoming, Wiencke John K, Witte John S, Wrensch Margaret, Wu Xifeng, Yamamura Yuko, Zanetti Krista A, Zheng Wei, Ziegler Regina G, Zhu Xiaofeng, Redline Susan, Hirschhorn Joel N, Henderson Brian E, Taylor Herman A, Price Alkes L, Hakonarson Hakon, Chanock Stephen J, Haiman Christopher A, Wilson James G, Reich David, Myers Simon |
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction. Human genetics 2012 Sep 131 (9): 1519-24. Borel Christelle, Cheung Fanny, Stewart Helen, Koolen David A, Phillips Christopher, Thomas N Simon, Jacobs Patricia A, Eliez Stephan, Sharp Andrew |
Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome research 2013 Mar 23 (3): 419-30. Hussin Julie, Sinnett Daniel, Casals Ferran, Idaghdour Youssef, Bruat Vanessa, Saillour Virginie, Healy Jasmine, Grenier Jean-Christophe, de Malliard Thibault, Busche Stephan, Spinella Jean-François, Larivière Mathieu, Gibson Greg, Andersson Anna, Holmfeldt Linda, Ma Jing, Wei Lei, Zhang Jinghui, Andelfinger Gregor, Downing James R, Mullighan Charles G, Awadalla Phil |
PRDM9 gene polymorphism may not be associated with defective spermatogenesis in the Chinese Han population. Systems biology in reproductive medicine 2013 Feb 59 (1): 38-41. He Xiao-Jin, Ruan Jian, Du Wei-Dong, Cao Yun-Xia, Chen Gang, Zuo Xian-Bo, Peng Yu-Wan, Wu Huan, Song Bing, Zhang Xue-J |
Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal. PloS one 2015 10 (7): e0133422. Abrantes Patrícia, Santos Maria M, Sousa Inês, Xavier Joana M, Francisco Vânia, Krug Tiago, Sobral João, Matos Mafalda, Martins Madalena, Jacinto António, Coiteiro Domingos, Oliveira Sofia |
The non-coding landscape of head and neck squamous cell carcinoma. Oncotarget 2016 08 7 (32): 51211-51222. Zou Angela E, Zheng Hao, Saad Maarouf A, Rahimy Mehran, Ku Jonjei, Kuo Selena Z, Honda Thomas K, Wang-Rodriguez Jessica, Xuan Yinan, Korrapati Avinaash, Yu Vicky, Singh Pranav, Grandis Jennifer R, King Charles C, Lippman Scott M, Wang Xiao Qi, Hinton Andrew, Ongkeko Weg |
Health and population effects of rare gene knockouts in adult humans with related parents. Science (New York, N.Y.) 2016 Mar . Narasimhan Vagheesh M, Hunt Karen A, Mason Dan, Baker Christopher L, Karczewski Konrad J, Barnes Michael R, Barnett Anthony H, Bates Chris, Bellary Srikanth, Bockett Nicholas A, Giorda Kristina, Griffiths Christopher J, Hemingway Harry, Jia Zhilong, Kelly M Ann, Khawaja Hajrah A, Lek Monkol, McCarthy Shane, McEachan Rosie, O'Donnell-Luria Anne, Paigen Kenneth, Parisinos Constantinos A, Sheridan Eamonn, Southgate Laura, Tee Louise, Thomas Mark, Xue Yali, Schnall-Levin Michael, Petkov Petko M, Tyler-Smith Chris, Maher Eamonn R, Trembath Richard C, MacArthur Daniel G, Wright John, Durbin Richard, van Heel David |
Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin. Journal of Down Syndrome & chromosome abnormalities 2016 Dec 2 (2): . Oliver Tiffany Renee, Middlebrooks Candace, Harden Ariel, Scott Nyeisha, Johnson Blair, Jones Jillian, Walker Christin, Wilkerson Corinthia, Saffold Sha-Hanna, Akinseye Abisola, Smith Tunde, Feingold Eleanor, Sherman Stephanie |
An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome. Scientific reports 2017 Jan 7 40031. Vergés Laia, Vidal Francesca, Geán Esther, Alemany-Schmidt Alexandra, Oliver-Bonet Maria, Blanco Jo |
Genetic Risk Factors for Intracranial Aneurysm in the Kazakh Population. Journal of molecular neuroscience : MN 2018 Aug . Zholdybayeva Elena V, Medetov Yerkin Z, Aitkulova Akbota M, Makhambetov Yerbol T, Akshulakov Serik K, Kaliyev Assylbek B, Talzhanov Yerkebulan A, Kulmambetova Gulmira N, Iskakova Aisha N, Ramankulov Yerlan |
Bos taurus-indicus hybridization correlates with intralocus sexual-conflict effects of PRDM9 on male and female fertility in Holstein cattle. BMC genetics 2019 Aug 20 (1): 71. Seroussi Eyal, Shirak Andrey, Gershoni Moran, Ezra Ephraim, de Abreu Santos Daniel Jordan, Ma Li, Liu George |
Variant Identification in BARD1, PRDM9, RCC1, and RECQL in Patients with Ovarian Cancer by Targeted Next-generation Sequencing of DNA Pools. Cancer prevention research (Philadelphia, Pa.) 2021 12 15 (3): 151-160. Suszynska Malwina, Ratajska Magdalena, Galka-Marciniak Paulina, Ryszkowska Aleksandra, Wydra Dariusz, Debniak Jaroslaw, Jasiak Anna, Wasag Bartosz, Cybulski Cezary, Kozlowski Pio |
Association of Single Nucleotide Polymorphisms in the PYGO2 and PRDM9 Genes with Idiopathic Azoospermia in Iranian Infertile Male Patients. Iranian journal of medical sciences 2023 1 48 (1): 77-84. Soleymani Moud Sanaz, Kamal Seraji Katayun, Ramezani Mina, Piravar Zeyn |
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- Page last updated:Apr 22, 2024
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