Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: HAND2[original query] |
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Transcription factor HAND2 mutations in sporadic Chinese patients with congenital heart disease. Chinese medical journal 2010 Jul 123 (13): 1623-7. Shen Lei, Li Xiao-Feng, Shen A-Dong, Wang Qiang, Liu Cai-Xia, Guo Ya-Jie, Song Zhen-Jiang, Li Zhong-Z |
Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. American journal of human genetics 2012 Sep 91 (3): 489-501. Soemedi Rachel, Wilson Ian J, Bentham Jamie, Darlay Rebecca, Töpf Ana, Zelenika Diana, Cosgrove Catherine, Setchfield Kerry, Thornborough Chris, Granados-Riveron Javier, Blue Gillian M, Breckpot Jeroen, Hellens Stephen, Zwolinkski Simon, Glen Elise, Mamasoula Chrysovalanto, Rahman Thahira J, Hall Darroch, Rauch Anita, Devriendt Koenraad, Gewillig Marc, O' Sullivan John, Winlaw David S, Bu'Lock Frances, Brook J David, Bhattacharya Shoumo, Lathrop Mark, Santibanez-Koref Mauro, Cordell Heather J, Goodship Judith A, Keavney Bernard |
Expression of genes involved in progesterone receptor paracrine signaling and their effect on litter size in pigs. Journal of animal science and biotechnology 2016 7 31. Chen Xiao, Fu Jinluan, Wang Aig |
Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci.
European heart journal 2017 Apr . Lee Ji-Young, Kim Tae-Hoon, Yang Pil-Sung, Lim Hong Euy, Choi Eue-Keun, Shim Jaemin, Shin Eunsoon, Uhm Jae-Sun, Kim Jin-Seok, Joung Boyoung, Oh Seil, Lee Moon-Hyoung, Kim Young-Hoon, Pak Hui-N |
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Nature genetics 2017 Apr . Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, , Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihi |
ASCL1 is a MYCN- and LMO1-dependent member of the adrenergic neuroblastoma core regulatory circuitry. Nature communications 2019 12 10 (1): 5622. Wang Lu, Tan Tze King, Durbin Adam D, Zimmerman Mark W, Abraham Brian J, Tan Shi Hao, Ngoc Phuong Cao Thi, Weichert-Leahey Nina, Akahane Koshi, Lawton Lee N, Rokita Jo Lynne, Maris John M, Young Richard A, Look A Thomas, Sanda Takao |
Predicting atrial fibrillation using a combination of genetic risk score and clinical risk factors. Heart rhythm 2020 Jan . Okubo Yousaku, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Tokuyama Takehito, Motoda Chikaaki, Amioka Michitaka, Hironobe Naoya, Okamura Sho, Ikeuchi Yoshihiro, Miyauchi Syunsuke, Chayama Kazuaki, Kihara Yasu |
HAND2-AS1 rs2276941 Polymorphism Affecting the Binding of hsa-miR-1275 Is Associated with the Risk of Colorectal Cancer. DNA and cell biology 2022 Jun 41 (6): 600-605. Gao Xueren, Zhang Shulong, Wang Xiaoti |
Construction and Validation of a Novel Pyroptosis-Related Four-lncRNA Prognostic Signature Related to Gastric Cancer and Immune Infiltration. Frontiers in immunology 2022 4 13 854785. Wang Zhengguang, Cao Lei, Zhou Sitong, Lyu Jin, Gao Yang, Yang Rongh |
Somatic Mutations Enriched in Cis-Regulatory Elements Affect Genes Involved in Embryonic Development and Immune System Response in Neuroblastoma. Cancer research 2022 2 82 (7): 1193-1207. Lasorsa Vito Alessandro, Montella Annalaura, Cantalupo Sueva, Tirelli Matilde, de Torres Carmen, Aveic Sanja, Tonini Gian Paolo, Iolascon Achille, Capasso Mar |
CFDP1 is a neuroblastoma susceptibility gene that regulates transcription factors of the noradrenergic cell identity. HGG advances 2022 11 4 (1): 100158. Formicola Daniela, Lasorsa Vito Alessandro, Cantalupo Sueva, Testori Alessandro, Cardinale Antonella, Avitabile Marianna, Diskin Sharon, Iolascon Achille, Capasso Mar |
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease.
Nature genetics 2022 6 54 (6): 772-782. Tcheandjieu Catherine, Xiao Ke, Tejeda Helio, Lynch Julie A, Ruotsalainen Sanni, Bellomo Tiffany, Palnati Madhuri, Judy Renae, Klarin Derek, Kember Rachel L, Verma Shefali, , , , Palotie Aarno, Daly Mark, Ritchie Marylyn, Rader Daniel J, Rivas Manuel A, Assimes Themistocles, Tsao Philip, Damrauer Scott, Priest James |
Pregnancy-Associated Bleeding and Genetics: Five Sequence Variants in the Myometrium and Progesterone Signaling Pathway are associated with postpartum hemorrhage. medRxiv : the preprint server for health sciences 2023 8 . David Westergaard, Valgerdur Steinthorsdottir, Lilja Stefansdottir, Palle Duun Rohde, Xiaoping Wu, Frank Geller, Jaakko Tyrmi, Aki S Havulinna, Pol Sole Navais, Christopher Flatley, Sisse Rye Ostrowski, Ole Birger Pedersen, Christian Erikstrup, Erik Sørensen, Christina Mikkelsen, Mie Topholm Brun, Bitten Aagaard Jensen, Thorsten Brodersen, Henrik Ullum, , , , , Per Magnus, Ole A Andreassen, Pål R Njolstad, Astrid Marie Kolte, Lone Krebs, Mette Nyegaard, Thomas Folkmann Hansen, Bjarke Fenstra, Mark Daly, Cecilia M Lindgren, Gudmar Thorleifsson, Olafur A Stefansson, Gardar Sveinbjornsson, Daniel F Gudbjartsson, Unnur Thorsteinsdottir, Karina Banasik, Bo Jacobsson, Triin Laisk, Hannele Laivuori, Kari Stefansson, Søren Brunak, Henriette Svarre Niels |
Molecular Genetic Study on HAND2 Gene Promoter in Ventricular Septal Defect. International heart journal 2023 11 64 (6): 1140-1147. Meikun Li, Yahui Cai, Shuchao Pang, Bo Y |
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