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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and HAND2[original query]
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
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. GWAS Catalog
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
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. GWAS Catalog
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
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
Combining genetic and single-cell expression data reveals cell types and novel candidate genes for orofacial clefting.
Scientific reports 2024 11 14 (1): 26492.
Anna Siewert, Simone Hoeland, Elisabeth Mangold, Kerstin U Ludw
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