Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: DLK1[original query] |
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Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans. European journal of human genetics : EJHG 2008 Sep 16 (9): 1126-34. Wermter Anne-Kathrin, Scherag André, Meyre David, Reichwald Kathrin, Durand Emmanuelle, Nguyen Thuy Trang, Koberwitz Kerstin, Lichtner Peter, Meitinger Thomas, Schäfer Helmut, Hinney Anke, Froguel Philippe, Hebebrand Johannes, Brönner Günt |
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.
Nature genetics 2010 Jan 42 (1): 68-71. Wallace Chris, Smyth Deborah J, Maisuria-Armer Meeta, Walker Neil M, Todd John A, Clayton David |
An upstream insulator regulates DLK1 imprinting in AML. Blood 2010 1 115 (11): 2260-3. Khoury Haytham, Suarez-Saiz Fernando, Wu Samantha, Minden Mark |
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 |
High-dose folic acid supplementation alters the human sperm methylome and is influenced by the MTHFR C677T polymorphism. Human molecular genetics 2015 Aug . Aarabi Mahmoud, San Gabriel Maria C, Chan Donovan, Behan Nathalie A, Caron Maxime, Pastinen Tomi, Bourque Guillaume, MacFarlane Amanda J, Zini Armand, Trasler Jacquet |
Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus. Leukemia 2015 May . Chase A, Leung W, Tapper W, Jones A V, Knoops L, Rasi C, Forsberg L A, Guglielmelli P, Zoi K, Hall V, Chiecchio L, Eder-Azanza L, Bryant C, Lannfelt L, Docherty L, White H E, Score J, Mackay D J G, Vannucchi A M, Dumanski J P, Cross N C |
Genetic link of type 1 diabetes susceptibility loci with rheumatoid arthritis in Pakistani patients. Immunogenetics 2015 Jun 67 (5-6): 277-82. Kiani Aysha Karim, Jahangir Sidrah, Jahngir Sidrah, John Peter, Bhatti Attya, Zia Asima, Wang Xingbin, Demirci F Yesim, Kamboh M Ily |
Polygenic associations of neurodevelopmental genes in suicide attempt. Molecular psychiatry 2015 Dec . Sokolowski M, Wasserman J, Wasserman |
Associations Between Fetal Imprinted Genes and Maternal Blood Pressure in Pregnancy. Hypertension (Dallas, Tex. : 1979) 2016 Oct . Petry Clive J, Sanz Marcos Nuria, Pimentel Gracielle, Hayes M Geoffrey, Nodzenski Michael, Scholtens Denise M, Hughes Ieuan A, Acerini Carlo L, Ong Ken K, Lowe William L, Dunger David |
Molecular Screening of MKRN3, DLK1, and KCNK9 Genes in Girls with Idiopathic Central Precocious Puberty. Hormone research in paediatrics 2017 Jul . Grandone Anna, Capristo Carlo, Cirillo Grazia, Sasso Marcella, Umano Giuseppina Rosaria, Mariani Michela, Miraglia Del Giudice Emanuele, Perrone Lau |
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature genetics 2017 Jun 49 (6): 834-841. Day Felix R, Thompson Deborah J, Helgason Hannes, Chasman Daniel I, Finucane Hilary, Sulem Patrick, Ruth Katherine S, Whalen Sean, Sarkar Abhishek K, Albrecht Eva, Altmaier Elisabeth, Amini Marzyeh, Barbieri Caterina M, Boutin Thibaud, Campbell Archie, Demerath Ellen, Giri Ayush, He Chunyan, Hottenga Jouke J, Karlsson Robert, Kolcic Ivana, Loh Po-Ru, Lunetta Kathryn L, Mangino Massimo, Marco Brumat, McMahon George, Medland Sarah E, Nolte Ilja M, Noordam Raymond, Nutile Teresa, Paternoster Lavinia, Perjakova Natalia, Porcu Eleonora, Rose Lynda M, Schraut Katharina E, Segrè Ayellet V, Smith Albert V, Stolk Lisette, Teumer Alexander, Andrulis Irene L, Bandinelli Stefania, Beckmann Matthias W, Benitez Javier, Bergmann Sven, Bochud Murielle, Boerwinkle Eric, Bojesen Stig E, Bolla Manjeet K, Brand Judith S, Brauch Hiltrud, Brenner Hermann, Broer Linda, Brüning Thomas, Buring Julie E, Campbell Harry, Catamo Eulalia, Chanock Stephen, Chenevix-Trench Georgia, Corre Tanguy, Couch Fergus J, Cousminer Diana L, Cox Angela, Crisponi Laura, Czene Kamila, Davey Smith George, de Geus Eco J C N, de Mutsert Renée, De Vivo Immaculata, Dennis Joe, Devilee Peter, Dos-Santos-Silva Isabel, Dunning Alison M, Eriksson Johan G, Fasching Peter A, Fernández-Rhodes Lindsay, Ferrucci Luigi, Flesch-Janys Dieter, Franke Lude, Gabrielson Marike, Gandin Ilaria, Giles Graham G, Grallert Harald, Gudbjartsson Daniel F, Guénel Pascal, Hall Per, Hallberg Emily, Hamann Ute, Harris Tamara B, Hartman Catharina A, Heiss Gerardo, Hooning Maartje J, Hopper John L, Hu Frank, Hunter David J, Ikram M Arfan, Im Hae Kyung, Järvelin Marjo-Riitta, Joshi Peter K, Karasik David, Kellis Manolis, Kutalik Zoltan, LaChance Genevieve, Lambrechts Diether, Langenberg Claudia, Launer Lenore J, Laven Joop S E, Lenarduzzi Stefania, Li Jingmei, Lind Penelope A, Lindstrom Sara, Liu YongMei, Luan Jian'an, Mägi Reedik, Mannermaa Arto, Mbarek Hamdi, McCarthy Mark I, Meisinger Christa, Meitinger Thomas, Menni Cristina, Metspalu Andres, Michailidou Kyriaki, Milani Lili, Milne Roger L, Montgomery Grant W, Mulligan Anna M, Nalls Mike A, Navarro Pau, Nevanlinna Heli, Nyholt Dale R, Oldehinkel Albertine J, O'Mara Tracy A, Padmanabhan Sandosh, Palotie Aarno, Pedersen Nancy, Peters Annette, Peto Julian, Pharoah Paul D P, Pouta Anneli, Radice Paolo, Rahman Iffat, Ring Susan M, Robino Antonietta, Rosendaal Frits R, Rudan Igor, Rueedi Rico, Ruggiero Daniela, Sala Cinzia F, Schmidt Marjanka K, Scott Robert A, Shah Mitul, Sorice Rossella, Southey Melissa C, Sovio Ulla, Stampfer Meir, Steri Maristella, Strauch Konstantin, Tanaka Toshiko, Tikkanen Emmi, Timpson Nicholas J, Traglia Michela, Truong Thérèse, Tyrer Jonathan P, Uitterlinden André G, Edwards Digna R Velez, Vitart Veronique, Völker Uwe, Vollenweider Peter, Wang Qin, Widen Elisabeth, van Dijk Ko Willems, Willemsen Gonneke, Winqvist Robert, Wolffenbuttel Bruce H R, Zhao Jing Hua, Zoledziewska Magdalena, Zygmunt Marek, Alizadeh Behrooz Z, Boomsma Dorret I, Ciullo Marina, Cucca Francesco, Esko Tõnu, Franceschini Nora, Gieger Christian, Gudnason Vilmundur, Hayward Caroline, Kraft Peter, Lawlor Debbie A, Magnusson Patrik K E, Martin Nicholas G, Mook-Kanamori Dennis O, Nohr Ellen A, Polasek Ozren, Porteous David, Price Alkes L, Ridker Paul M, Snieder Harold, Spector Tim D, Stöckl Doris, Toniolo Daniela, Ulivi Sheila, Visser Jenny A, Völzke Henry, Wareham Nicholas J, Wilson James F, , , , , , , Spurdle Amanda B, Thorsteindottir Unnur, Pollard Katherine S, Easton Douglas F, Tung Joyce Y, Chang-Claude Jenny, Hinds David, Murray Anna, Murabito Joanne M, Stefansson Kari, Ong Ken K, Perry John R |
Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population. BMC research notes 2019 Aug 12 (1): 544. Aslam Muhammad Muaaz, John Peter, Fan Kang-Hsien, Bhatti Attya, Jahangir Sidrah, Feingold Eleanor, Demirci F Yesim, Kamboh M Ily |
Pioneering studies on monogenic central precocious puberty. Archives of endocrinology and metabolism 2019 8 63 (4): 438-444. Canton Ana Pinheiro Machado, Seraphim Carlos Eduardo, Brito Vinicius Nahime, Latronico Ana Claud |
Association study of DLK1 in girls with idiopathic central precocious puberty. Journal of pediatric endocrinology & metabolism : JPEM 2020 Jul . Lee Hae Sang, Kim Kyung Hee, Hwang Jin So |
Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish Study. The Journal of clinical endocrinology and metabolism 2020 7 105 (10): . Montenegro Luciana, Labarta José I, Piovesan Maira, Canton Ana P M, Corripio Raquel, Soriano-Guillén Leandro, Travieso-Suárez Lourdes, Martín-Rivada Álvaro, Barrios Vicente, Seraphim Carlos E, Brito Vinicius N, Latronico Ana Claudia, Argente Jes |
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 |
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical epigenetics 2020 6 12 (1): 86. Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa |
Analysis of the Bovine DLK1 Gene Polymorphism and Its Relation to Lipid Metabolism in Chinese Simmental. Animals : an open access journal from MDPI 2020 May 10 (6): . Wang Mengyan, Jiang Ping, Yu Xiang, Mi Jiaqi, Bai Zitong, Zhang Xiuqi, Liu Yinuo, Fang Xibi, Yang Runjun, Zhao Zhih |
Genetic Polymorphisms of Delta-Like 1 Homolog Influence the Susceptibility to Antituberculosis Drug-Induced Hepatotoxicity. DNA and cell biology 2020 Dec . Fu Yang, Liu Tangyuheng, Song Jiajia, Jiao Lin, Zhou Juan, Bai Hao, Zhao Zhenzhen, Chen Hao, Wu Tao, Lyv Mengyuan, Zhou Yi, Ying Binwu, Xu Yanmi |
Genetically predicted circulating protein biomarkers and ovarian cancer risk. Gynecologic oncology 2020 Nov . Considine Daniel P C, Jia Guochong, Shu Xiang, Schildkraut Joellen M, Pharoah Paul D P, Zheng Wei, Kar Siddhartha P, |
Functional multigenic variations associated with hodgkin lymphoma.
International journal of laboratory hematology 2021 Jul . Osman Yasser, Elsharkawy Tarek, Hashim Tariq Mohammad, Alratroot Jumana Abdulwahab, Alsuwat Hind Saleh, Otaibi Waad Mohammed Al, Hegazi Fatma Mohammed, AbdulAzeez Sayed, Borgio J Franc |
Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants. European journal of human genetics : EJHG 2021 7 29 (12): 1756-1761. Pham Aurélie, Sobrier Marie-Laure, Giabicani Eloïse, Le Jules Fernandes Marilyne, Mitanchez Delphine, Brioude Fréderic, Netchine Irè |
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 |
Genetic causes of central precocious puberty. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology 2022 8 31 (3): 101-109. Tajima Toshihi |
Circulating levels of DLK1 and glucose homeostasis in girls with obesity: A pilot study. Frontiers in endocrinology 2022 12 13 1033179. Palumbo Stefania, Umano Giuseppina Rosaria, Aiello Francesca, Cirillo Grazia, Miraglia Del Giudice Emanuele, Grandone An |
Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia. Hematology (Amsterdam, Netherlands) 2023 3 28 (1): 2187155. Hantaweepant Chattree, Suktitipat Bhoom, Pithukpakorn Manop, Chinthammitr Yingyong, Limwongse Chanin, Tansiri Nawaporn, Sawatnatee Surasak, Takpradit Chayamon, Rotchanapanya Wannaphorn, Pongudom Saranya, Charoenprasert Kanyaporn, Paiboonsukwong Kittiphong, Thamprasert Wichuda, Nolwachai Narumol, Rattanasawat Wanlapa, Sae-Aeng Busakorn, Khorwanichakij Nisachon, Saetow Putchong, Saengboon Supawee, Kamjornpreecha Krittichat, Pholmoo Wikanda, Dujjawan Boonyanuch, Siritanaratkul Noppad |
Clinical and genetic characterization of familial central precocious puberty. The Journal of clinical endocrinology and metabolism 2023 1 . Tinano Flávia Rezende, Canton Ana Pinheiro Machado, Montenegro Luciana R, de Castro Leal Andrea, Faria Aline G, Seraphim Carlos E, Brauner Raja, Jorge Alexander A, Mendonca Berenice B, Argente Jesús, Brito Vinicius N, Latronico Ana Claud |
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