Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: MAGEL2[original query] |
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Lack of association between MAGEL2 and schizophrenia and mood disorders in the Japanese population. Neuromolecular medicine 2010 Sep 12 (3): 285-91. Fukuo Yasuhisa, Kishi Taro, Okochi Tomo, Kitajima Tsuyoshi, Tsunoka Tomoko, Okumukura Takenori, Kinoshita Yoko, Kawashima Kunihiro, Yamanouchi Yoshio, Umene-Nakano Wakako, Naitoh Hiroshi, Inada Toshiya, Yoshimura Reiji, Nakamura Jun, Ozaki Norio, Iwata Nak |
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
Nature 2014 Oct 514 (7520): 92-7. Perry John R B, Day Felix, Elks Cathy E, Sulem Patrick, Thompson Deborah J, Ferreira Teresa, He Chunyan, Chasman Daniel I, Esko Tõnu, Thorleifsson Gudmar, Albrecht Eva, Ang Wei Q, Corre Tanguy, Cousminer Diana L, Feenstra Bjarke, Franceschini Nora, Ganna Andrea, Johnson Andrew D, Kjellqvist Sanela, Lunetta Kathryn L, McMahon George, Nolte Ilja M, Paternoster Lavinia, Porcu Eleonora, Smith Albert V, Stolk Lisette, Teumer Alexander, Tšernikova Natalia, Tikkanen Emmi, Ulivi Sheila, Wagner Erin K, Amin Najaf, Bierut Laura J, Byrne Enda M, Hottenga Jouke-Jan, Koller Daniel L, Mangino Massimo, Pers Tune H, Yerges-Armstrong Laura M, Hua Zhao Jing, Andrulis Irene L, Anton-Culver Hoda, Atsma Femke, Bandinelli Stefania, Beckmann Matthias W, Benitez Javier, Blomqvist Carl, Bojesen Stig E, Bolla Manjeet K, Bonanni Bernardo, Brauch Hiltrud, Brenner Hermann, Buring Julie E, Chang-Claude Jenny, Chanock Stephen, Chen Jinhui, Chenevix-Trench Georgia, Collée J Margriet, Couch Fergus J, Couper David, Coviello Andrea D, Cox Angela, Czene Kamila, D'adamo Adamo Pio, Davey Smith George, De Vivo Immaculata, Demerath Ellen W, Dennis Joe, Devilee Peter, Dieffenbach Aida K, Dunning Alison M, Eiriksdottir Gudny, Eriksson Johan G, Fasching Peter A, Ferrucci Luigi, Flesch-Janys Dieter, Flyger Henrik, Foroud Tatiana, Franke Lude, Garcia Melissa E, García-Closas Montserrat, Geller Frank, de Geus Eco E J, Giles Graham G, Gudbjartsson Daniel F, Gudnason Vilmundur, Guénel Pascal, Guo Suiqun, Hall Per, Hamann Ute, Haring Robin, Hartman Catharina A, Heath Andrew C, Hofman Albert, Hooning Maartje J, Hopper John L, Hu Frank B, Hunter David J, Karasik David, Kiel Douglas P, Knight Julia A, Kosma Veli-Matti, Kutalik Zoltan, Lai Sandra, Lambrechts Diether, Lindblom Annika, Mägi Reedik, Magnusson Patrik K, Mannermaa Arto, Martin Nicholas G, Masson Gisli, McArdle Patrick F, McArdle Wendy L, Melbye Mads, Michailidou Kyriaki, Mihailov Evelin, Milani Lili, Milne Roger L, Nevanlinna Heli, Neven Patrick, Nohr Ellen A, Oldehinkel Albertine J, Oostra Ben A, Palotie Aarno, Peacock Munro, Pedersen Nancy L, Peterlongo Paolo, Peto Julian, Pharoah Paul D P, Postma Dirkje S, Pouta Anneli, Pylkäs Katri, Radice Paolo, Ring Susan, Rivadeneira Fernando, Robino Antonietta, Rose Lynda M, Rudolph Anja, Salomaa Veikko, Sanna Serena, Schlessinger David, Schmidt Marjanka K, Southey Mellissa C, Sovio Ulla, Stampfer Meir J, Stöckl Doris, Storniolo Anna M, Timpson Nicholas J, Tyrer Jonathan, Visser Jenny A, Vollenweider Peter, Völzke Henry, Waeber Gerard, Waldenberger Melanie, Wallaschofski Henri, Wang Qin, Willemsen Gonneke, Winqvist Robert, Wolffenbuttel Bruce H R, Wright Margaret J, , , , , , , Boomsma Dorret I, Econs Michael J, Khaw Kay-Tee, Loos Ruth J F, McCarthy Mark I, Montgomery Grant W, Rice John P, Streeten Elizabeth A, Thorsteinsdottir Unnur, van Duijn Cornelia M, Alizadeh Behrooz Z, Bergmann Sven, Boerwinkle Eric, Boyd Heather A, Crisponi Laura, Gasparini Paolo, Gieger Christian, Harris Tamara B, Ingelsson Erik, Järvelin Marjo-Riitta, Kraft Peter, Lawlor Debbie, Metspalu Andres, Pennell Craig E, Ridker Paul M, Snieder Harold, Sørensen Thorkild I A, Spector Tim D, Strachan David P, Uitterlinden André G, Wareham Nicholas J, Widen Elisabeth, Zygmunt Marek, Murray Anna, Easton Douglas F, Stefansson Kari, Murabito Joanne M, Ong Ken |
MAGEL2-related disorders: A study and case series. Clinical genetics 2019 8 96 (6): 493-505. Patak Jameson, Gilfert James, Byler Melissa, Neerukonda Vamsee, Thiffault Isabelle, Cross Laura, Amudhavalli Shivarajan, Pacio-Miguez Marta, Palomares-Bralo Maria, Garcia-Minaur Sixto, Santos-Simarro Fernando, Powis Zoe, Alcaraz Wendy, Tang Sha, Jurgens Julie, Barry Brenda, England Eleina, Engle Elizabeth, Hess Jonathon, Lebel Robert |
Polysomnographic characteristics and sleep-disordered breathing in Schaaf-Yang syndrome. Pediatric pulmonology 2020 9 55 (11): 3162-3167. Powell Weston T, Schaaf Christian P, Rech Megan E, Wrede Joan |
Phenotypic spectrum and genetic analysis in the fatal cases of Schaaf-Yang syndrome: Two case reports and literature review. Medicine 2020 7 99 (29): e20574. Chen Xuefei, Ma Xiaolu, Zou Chaoch |
Heterozygous Deletions in MKRN3 Cause Central Precocious Puberty Without Prader-Willi Syndrome. The Journal of clinical endocrinology and metabolism 2020 6 105 (8): 2732-9. Meader Brooke N, Albano Alessandro, Sekizkardes Hilal, Delaney Ange |
Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty. Frontiers in endocrinology 2021 10 12 745048. Neocleous Vassos, Fanis Pavlos, Toumba Meropi, Gorka Barbara, Kousiappa Ioanna, Tanteles George A, Iasonides Michalis, Nicolaides Nicolas C, Christou Yiolanda P, Michailidou Kyriaki, Nicolaou Stella, Papacostas Savvas S, Christoforidis Athanasios, Kyriakou Andreas, Vlachakis Dimitrios, Skordis Nicos, Phylactou Leonidas |
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