Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: CCDC141[original query] |
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Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.
Schizophrenia bulletin 2017 May . Ortega-Alonso Alfredo, Ekelund Jesper, Sarin Antti-Pekka, Miettunen Jouko, Veijola Juha, Järvelin Marjo-Riitta, Hennah Willi |
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism. Clinical genetics 2019 Feb 95 (2): 320-324. Kotan Leman D, Isik Emregul, Turan Ihsan, Mengen Eda, Akkus Gamze, Tastan Mehmet, Gurbuz Fatih, Yuksel Bilgin, Topaloglu A Kem |
Combining CDKN1A gene expression and genome-wide SNPs in a twin cohort to gain insight into the heritability of individual radiosensitivity. Functional & integrative genomics 2019 2 19 (4): 575-585. Zyla Joanna, Kabacik Sylwia, O'Brien Grainne, Wakil Salma, Al-Harbi Najla, Kaprio Jaakko, Badie Christophe, Polanska Joanna, Alsbeih Gha |
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.
Molecular psychiatry 2019 Jan . Erzurumluoglu A Mesut, Liu Mengzhen, Jackson Victoria E, Barnes Daniel R, Datta Gargi, Melbourne Carl A, Young Robin, Batini Chiara, Surendran Praveen, Jiang Tao, Adnan Sheikh Daud, Afaq Saima, Agrawal Arpana, Altmaier Elisabeth, Antoniou Antonis C, Asselbergs Folkert W, Baumbach Clemens, Bierut Laura, Bertelsen Sarah, Boehnke Michael, Bots Michiel L, Brazel David M, Chambers John C, Chang-Claude Jenny, Chen Chu, Corley Janie, Chou Yi-Ling, David Sean P, de Boer Rudolf A, de Leeuw Christiaan A, Dennis Joe G, Dominiczak Anna F, Dunning Alison M, Easton Douglas F, Eaton Charles, Elliott Paul, Evangelou Evangelos, Faul Jessica D, Foroud Tatiana, Goate Alison, Gong Jian, Grabe Hans J, Haessler Jeff, Haiman Christopher, Hallmans Göran, Hammerschlag Anke R, Harris Sarah E, Hattersley Andrew, Heath Andrew, Hsu Chris, Iacono William G, Kanoni Stavroula, Kapoor Manav, Kaprio Jaakko, Kardia Sharon L, Karpe Fredrik, Kontto Jukka, Kooner Jaspal S, Kooperberg Charles, Kuulasmaa Kari, Laakso Markku, Lai Dongbing, Langenberg Claudia, Le Nhung, Lettre Guillaume, Loukola Anu, Luan Jian'an, Madden Pamela A F, Mangino Massimo, Marioni Riccardo E, Marouli Eirini, Marten Jonathan, Martin Nicholas G, McGue Matt, Michailidou Kyriaki, Mihailov Evelin, Moayyeri Alireza, Moitry Marie, Müller-Nurasyid Martina, Naheed Aliya, Nauck Matthias, Neville Matthew J, Nielsen Sune Fallgaard, North Kari, Perola Markus, Pharoah Paul D P, Pistis Giorgio, Polderman Tinca J, Posthuma Danielle, Poulter Neil, Qaiser Beenish, Rasheed Asif, Reiner Alex, Renström Frida, Rice John, Rohde Rebecca, Rolandsson Olov, Samani Nilesh J, Samuel Maria, Schlessinger David, Scholte Steven H, Scott Robert A, Sever Peter, Shao Yaming, Shrine Nick, Smith Jennifer A, Starr John M, Stirrups Kathleen, Stram Danielle, Stringham Heather M, Tachmazidou Ioanna, Tardif Jean-Claude, Thompson Deborah J, Tindle Hilary A, Tragante Vinicius, Trompet Stella, Turcot Valerie, Tyrrell Jessica, Vaartjes Ilonca, van der Leij Andries R, van der Meer Peter, Varga Tibor V, Verweij Niek, Völzke Henry, Wareham Nicholas J, Warren Helen R, Weir David R, Weiss Stefan, Wetherill Leah, Yaghootkar Hanieh, Yavas Ersin, Jiang Yu, Chen Fang, Zhan Xiaowei, Zhang Weihua, Zhao Wei, Zhao Wei, Zhou Kaixin, Amouyel Philippe, Blankenberg Stefan, Caulfield Mark J, Chowdhury Rajiv, Cucca Francesco, Deary Ian J, Deloukas Panos, Di Angelantonio Emanuele, Ferrario Marco, Ferrières Jean, Franks Paul W, Frayling Tim M, Frossard Philippe, Hall Ian P, Hayward Caroline, Jansson Jan-Håkan, Jukema J Wouter, Kee Frank, Männistö Satu, Metspalu Andres, Munroe Patricia B, Nordestgaard Børge Grønne, Palmer Colin N A, Salomaa Veikko, Sattar Naveed, Spector Timothy, Strachan David Peter, , van der Harst Pim, Zeggini Eleftheria, Saleheen Danish, Butterworth Adam S, Wain Louise V, Abecasis Goncalo R, Danesh John, Tobin Martin D, Vrieze Scott, Liu Dajiang J, Howson Joanna M |
Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism. European journal of endocrinology 2020 6 183 (3): 245-254. Hou Qiao, Wu Jiayu, Zhao Yaguang, Wang Xinying, Jiang Fang, Chen Dan-Na, Zheng Ruizhi, Men Meichao, Li Jia- |
Whole exome sequencing and trio analysis to broaden the variant spectrum of genes in idiopathic hypogonadotropic hypogonadism. Asian journal of andrology 2020 11 23 (3): 288-293. Zhang Jian, Tang Shu-Yan, Zhu Xiao-Bin, Li Peng, Lu Jian-Qi, Cong Jiang-Shan, Wang Ling-Bo, Zhang Feng, Li Zhe |
Mutations of METTL3 predict response to neoadjuvant chemotherapy in muscle-invasive bladder cancer. Journal of clinical and translational research 2021 7 7 (3): 386-413. Yang Zhao, Shen Zongyi, Jin Di, Zhang Nan, Wang Yue, Lei Wanjun, Zhang Zhiming, Chen Haige, Naz Faiza, Xu Lida, Wang Lei, Wang Shihui, Su Xin, Yu Changyuan, Li Cho |
Genetic insight into sick sinus syndrome.
European heart journal 2021 Feb . Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty. NPJ genomic medicine 2021 12 6 (1): 107. Saengkaew Tansit, Ruiz-Babot Gerard, David Alessia, Mancini Alessandra, Mariniello Katia, Cabrera Claudia P, Barnes Michael R, Dunkel Leo, Guasti Leonardo, Howard Sasha |
Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs. The journal of headache and pain 2022 3 23 (1): 39. Jiang Yun-Jin, Fann Cathy Shen-Jang, Fuh Jong-Ling, Chung Ming-Yi, Huang Hui-Ying, Chu Kuo-Chang, Wang Yen-Feng, Hsu Chia-Lin, Kao Lung-Sen, Chen Shih-Pin, Wang Shuu-Ji |
Genetic insight into sick sinus syndrome.
European heart journal 2021 May 42 (20): 1959-1971. Thorolfsdottir Rosa B, Sveinbjornsson Gardar, Aegisdottir Hildur M, Benonisdottir Stefania, Stefansdottir Lilja, Ivarsdottir Erna V, Halldorsson Gisli H, Sigurdsson Jon K, Torp-Pedersen Christian, Weeke Peter E, Brunak Søren, Westergaard David, Pedersen Ole B, Sorensen Erik, Nielsen Kaspar R, Burgdorf Kristoffer S, Banasik Karina, Brumpton Ben, Zhou Wei, Oddsson Asmundur, Tragante Vinicius, Hjorleifsson Kristjan E, Davidsson Olafur B, Rajamani Sridharan, Jonsson Stefan, Torfason Bjarni, Valgardsson Atli S, Thorgeirsson Gudmundur, Frigge Michael L, Thorleifsson Gudmar, Norddahl Gudmundur L, Helgadottir Anna, Gretarsdottir Solveig, Sulem Patrick, Jonsdottir Ingileif, Willer Cristen J, Hveem Kristian, Bundgaard Henning, Ullum Henrik, Arnar David O, Thorsteinsdottir Unnur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Kari, |
Genetic Determinants of Atherogenic Indexes. Genes 2023 6 14 (6): . Tomas Texis, Susana Rivera-Mancía, Eloisa Colín-Ramírez, Raul Cartas-Rosado, David Koepsell, Kenneth Rubio-Carrasco, Mauricio Rodríguez-Dorantes, Vanessa Gonzalez-Covarrubi |
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- Page last updated:Apr 16, 2024
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