Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: EDA2R[original query] |
---|
EDA2R is associated with androgenetic alopecia. The Journal of investigative dermatology 2008 Sep 128 (9): 2268-70. Prodi Dionigio Antonio, Pirastu Nicola, Maninchedda Giuseppe, Sassu Alessandro, Picciau Andrea, Palmas Maria Antonietta, Mossa Alessandra, Persico Ivana, Adamo Mauro, Angius Andrea, Pirastu Mar |
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.
The British journal of dermatology 2011 Dec 165 (6): 1293-302. Brockschmidt F F, Heilmann S, Ellis J A, Eigelshoven S, Hanneken S, Herold C, Moebus S, Alblas M A, Lippke B, Kluck N, Priebe L, Degenhardt F A, Jamra R A, Meesters C, Jöckel K-H, Erbel R, Harrap S, Schumacher J, Fröhlich H, Kruse R, Hillmer A M, Becker T, Nöthen M |
Genetic variants at 20p11 confer risk to androgenetic alopecia in the Chinese Han population. PloS one 2013 8 (8): e71771. Liang Bo, Yang Chunjun, Zuo Xianbo, Li Yang, Ding Yantao, Sheng Yujun, Zhou Fusheng, Cheng Hui, Zheng Xiaodong, Chen Gang, Zhu Zhengwei, Zhu Jun, Fu Xuhui, Wang Tao, Dong Ying, Duan Dawei, Tang Xianfa, Tang Huayang, Gao Jinping, Sun Liangdan, Yang Sen, Zhang Xuej |
Poor survival with wild-type TP53 ovarian cancer? Gynecologic oncology 2013 Sep 130 (3): 565-9. Wong Kwong-Kwok, Izaguirre Daisy I, Kwan Suet-Yan, King Erin R, Deavers Michael T, Sood Anil K, Mok Samuel C, Gershenson David |
Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss. Archives of dermatological research 2014 May 306 (4): 413-8. Nuwaihyd Rima, Redler Silke, Heilmann Stefanie, Drichel Dmitriy, Wolf Sabrina, Birch Pattie, Dobson Kathy, Lutz Gerhard, Giehl Kathrin A, Kruse Roland, Tazi-Ahnini Rachid, Hanneken Sandra, Böhm Markus, Miesel Anja, Fischer Tobias, Wolff Hans, Becker Tim, Garcia-Bartels Natalie, Blume-Peytavi Ulrike, Nöthen Markus M, Messenger Andrew G, Betz Regina |
Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements. Journal of human genetics 2016 Jun . Wohlfart Sigrun, Hammersen Johanna, Schneider Ho |
Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing. Journal of neurogenetics 2015 Dec 29 (4): 188-94. Jiang Yue, Wu Rong, Chen Chen, You Zhi-Fei, Luo Xingguang, Wang Xiao-Pi |
Genome-wide association study of loss of heterozygosity and metastasis-free survival in breast cancer patients. Experimental oncology 2018 2 39 (2): 145-150. Deryusheva I V, Tsyganov M, Garbukov E Y, Ibragimova M K, Kzhyshkovska Ju G, Slonimskaya E, Cherdyntseva N V, Litviakov N |
Identification of a Costimulatory Molecule-Related Signature for Predicting Prognostic Risk in Prostate Cancer. Frontiers in genetics 2021 9 12 666300. Ge Shengdong, Hua Xiaoliang, Chen Juan, Xiao Haibing, Zhang Li, Zhou Jun, Liang Chaozhao, Tai She |
Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss. Nature communications 2023 9 14 (1): 5492. Sabrina Katrin Henne, Rana Aldisi, Sugirthan Sivalingam, Lara Maleen Hochfeld, Oleg Borisov, Peter Michael Krawitz, Carlo Maj, Markus Maria Nöthen, Stefanie Heilmann-Heimba |
Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men. bioRxiv : the preprint server for biology 2024 1 . Rohini Janivara, Ujani Hazra, Aaron Pfennig, Maxine Harlemon, Michelle S Kim, Muthukrishnan Eaaswarkhanth, Wenlong C Chen, Adebola Ogunbiyi, Paidamoyo Kachambwa, Lindsay N Petersen, Mohamed Jalloh, James E Mensah, Andrew A Adjei, Ben Adusei, Maureen Joffe, Serigne M Gueye, Oseremen I Aisuodionoe-Shadrach, Pedro W Fernandez, Thomas E Rohan, Caroline Andrews, Timothy R Rebbeck, Akindele O Adebiyi, Ilir Agalliu, Joseph Lachan |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: