Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: MCM9[original query] |
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Pathogenic germline MCM9 variants are rare in Australian Lynch-like syndrome patients. Cancer genetics 2016 Nov 209 (11): 497-500. Liu Qing, Hesson Luke B, Nunez Andrea C, Packham Deborah, Hawkins Nicholas J, Ward Robyn L, Sloane Mathew |
MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism 2016 Nov jc20162565. Desai Swapna, Wood-Trageser Michelle, Matic Jelena, Chipkin Jaqueline, Jiang Huaiyang, Bachelot Anne, Dulon Jerome, Sala Cinzia, Barbieri Caterina, Cocca Massimiliano, Toniolo Daniela, Philippe Touraine, Witchel Selma, Rajkovic Aleksand |
Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency. Journal of assisted reproduction and genetics 2018 11 36 (1): 39-45. Yang Xiang, Touraine Philippe, Desai Swapna, Humphreys Gregory, Jiang Huaiyang, Yatsenko Alexander, Rajkovic Aleksand |
Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1- and MSH3-associated polyposes. Human mutation 2019 Jun . Terradas Mariona, Munoz-Torres Pau M, Belhadj Sami, Aiza Gemma, Navarro Matilde, Brunet Joan, Capellá Gabriel, Valle Lau |
Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention. Journal of ovarian research 2020 9 13 (1): 114. Liu Hongli, Wei Xiaoli, Sha Yanwei, Liu Wensheng, Gao Haijie, Lin Jin, Li Youzhu, Tang Yaling, Wang Yifeng, Wang Yanlong, Su Zhiyi |
Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes. Human molecular genetics 2020 May . Chen Shitao, Wang Guishuan, Zheng Xiaoguo, Ge Shunna, Dai Yubing, Ping Ping, Chen Xiangfeng, Liu Guihua, Zhang Jing, Yang Yang, Zhang Xinzong, Zhong An, Zhu Yongtong, Chu Qingjun, Huang Yonghan, Zhang Yong, Shen Changli, Yuan Yiming, Yuan Qilong, Pei Xiuying, Cheng C Yan, Sun F |
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human mutation 2020 May . Belhadj Sami, Terradas Mariona, Munoz-Torres Pau M, Aiza Gemma, Navarro Matilde, Capellá Gabriel, Valle Lau |
Novel pathogenic mutations in minichromosome maintenance complex component 9 (MCM9) responsible for premature ovarian insufficiency. Fertility and sterility 2020 3 113 (4): 845-852. Guo Ting, Zheng Ye, Li Guangyu, Zhao Shidou, Ma Jinlong, Qin Yingyi |
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency. PloS one 2020 10 15 (10): e0240795. França Monica M, Funari Mariana F A, Lerario Antonio M, Santos Mariza G, Nishi Mirian Y, Domenice Sorahia, Moraes Daniela R, Costalonga Everlayny F, Maciel Gustavo A R, Maciel-Guerra Andrea T, Guerra-Junior Gil, Mendonca Berenice |
Potential Prospective Biomarkers for Non-small Cell Lung Cancer: Mini-Chromosome Maintenance Proteins. Frontiers in genetics 2021 5 12 587017. Huang Chen, Lei Chuqi, Pan Boyu, Fang Senbiao, Chen Yubao, Cao Wenfeng, Liu Lir |
Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism. Journal of pediatric endocrinology & metabolism : JPEM 2021 4 34 (6): 771-780. Turkyilmaz Ayberk, Cayir Atilla, Yarali Oguzhan, Kurnaz Erdal, Kartal Baykan Emine, Arslan Ates Esra, Demirbilek Husey |
Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing. Journal of assisted reproduction and genetics 2021 Feb . Shen Jiandong, Qu Dianyun, Gao Yan, Sun Fangxi, Xie Jiazi, Sun Xueping, Wang Daowu, Ma Xiang, Cui Yugui, Liu Jiayin, Diao Feiya |
Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants. Molecular genetics & genomic medicine 2021 10 9 (12): e1831. Dell'Elice Anastasia, Cini Giulia, Fornasarig Mara, Armelao Franco, Barana Daniela, Bianchi Francesca, Casalis Cavalchini Guido Claudio, Maffè Antonella, Mammi Isabella, Pedroni Monica, Percesepe Antonio, Sorrentini Italo, Tibiletti Mariagrazia, Maestro Roberta, Quaia Michele, Viel Alessand |
ROS1 genomic rearrangements are rare actionable drivers in microsatellite stable colorectal cancer. International journal of cancer 2022 Aug . Akhoundova Dilara, Hussung Saskia, Sivakumar Smruthy, Töpfer Antonia, Rechsteiner Markus, Kahraman Abdullah, Arnold Fabian, Angst Florian, Britschgi Christian, Zoche Martin, Moch Holger, Weber Achim, Sokol Ethan, Fritsch Ralph |
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- Page last updated:Apr 22, 2024
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