Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: GH1[original query] |
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Genetic variation in IGF-1 and breast cancer risk in Ashkenazi carriers and noncarriers of BRCA1/2 mutations. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2009 Jun . Khoury-Shakour S, Lejbkowicz F, Barnett-Griness O, Tamir A, Pinchev M, Rennert G |
Body size, IGF and growth hormone polymorphisms, and colorectal adenomas and hyperplastic polyps. Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 2010 Aug 20 (4): 305-9. Wernli Karen J, Newcomb Polly A, Wang Yinghui, Makar Karen W, Shadman Mazyar, Chia Victoria M, Burnett-Hartman Andrea, Wurscher Michelle A, Zheng Yingye, Mandelson Margaret |
Genetic polymorphisms in the locus control region and promoter of GH1 are related to serum IGF-I levels and height in patients with isolated growth hormone deficiency and healthy controls. Hormone research in pædiatrics 2010 73 (1): 25-34. de Graaff Laura C G, Argente Jesus, van Meurs Joyce B J, Uitterlinden André G, Hokken-Koelega Anita C |
Relationship between growth hormone 1 genetic polymorphism and susceptibility to colorectal cancer. Journal of human genetics 2010 Mar 55 (3): 163-6. Gao Chang-Ming, Gong Jian-Ping, Wu Jian-Zhong, Cao Hai-Xia, Ding Jian-Hua, Zhou Jian-Nong, Liu Yan-Ting, Li Su-Ping, Cao Jia, Matsuo Keitaro, Takezaki Toshiro, Tajima Kaz |
Absence of GH-releasing hormone (GHRH) mutations in selected patients with isolated GH deficiency. The Journal of clinical endocrinology and metabolism 2011 Sep 96 (9): E1457-60. França Marcela M, Jorge Alexander A L, Alatzoglou Kyriaki S, Carvalho Luciani R S, Mendonca Berenice B, Audi Laura, Carrascosa Antonio, Dattani Mehul T, Arnhold Ivo J |
Polymorphisms in the pituitary growth hormone gene and its receptor associated with coronary artery disease in a predisposed cohort from India. Journal of genetics 2010 Dec 89 (4): 437-47. Maitra Arindam, Shanker Jayashree, Dash Debabrata, Sannappa Prathima R, John Shibu, Siwach Pratibha, Rao Veena S, Sridhara H, Kakkar Vijay |
Contribution of human growth hormone-releasing hormone receptor (GHRHR) gene sequence variation to isolated severe growth hormone deficiency (ISGHD) and normal adult height. Clinical endocrinology 2012 Oct 77 (4): 564-74. Camats Núria, Fernández-Cancio Mónica, Carrascosa Antonio, Andaluz Pilar, Albisu M Ángeles, Clemente María, Gussinyé Miquel, Yeste Diego, Audí Lau |
Pituitary stalk interruption syndrome in 58 Chinese patients: clinical features and genetic analysis. Clinical endocrinology 2012 Dec . Yang Y, Guo QH, Wang BA, Dou JT, Lv ZH, Ba JM, Lu JM, Pan CY, Mu YM |
A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme. PloS one 2012 7 (1): e29883. Alfred Tamuno, Ben-Shlomo Yoav, Cooper Rachel, Hardy Rebecca, Cooper Cyrus, Deary Ian J, Gaunt Tom R, Gunnell David, Harris Sarah E, Kumari Meena, Martin Richard M, Sayer Avan Aihie, Starr John M, Kuh Diana, Day Ian N M, |
Association analysis of ten candidate genes in a large multinational cohort of small for gestational age children and children with idiopathic short stature (NESTEGG study). Hormone research in pædiatrics 2013 80 (6): 466-76. de Graaff L C G, Clark A J L, Tauber M, Ranke M B, Johnston L B, Caliebe J, Molinas C, Amin N, van Duijn C, Wollmann H, Wallaschofski H, Savage M O, Hokken-Koelega A C |
Does HCV Patients Who Have BCL2 43Ala Genotype and Normal GH1 Levels Can Achieve Response to IFN Based Therapy? Indian journal of clinical biochemistry : IJCB 2012 Oct 27 (4): 344-50. Eskander Emad F, Abd-Rabou Ahmed A, Mohamed Mervat S, Yahya Shaymaa M M, Shaker Olfat |
GH1 T1663A polymorphism and cancer risk: a meta-analysis of case-control studies. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 May 35 (5): 4529-38. Shi Jing, Tong Jian-Huan, Cai Shua |
Growth Hormone 1 T1663A Polymorphism, Recreational Physical Activity and BMI, and Breast Cancer Risk in Chinese Women. Asian Pacific journal of cancer prevention : APJCP 2015 16 (13): 5421-5. Gao Chang-Ming, Ding Jian-Hua, Wu Jian-Shong, Cao Hai-Xia, Li Su-Ping, Liu Yan-Ting, Tang Jin-Hai, Tajima Kaz |
Genetic variation and effects of candidate-gene polymorphisms on coagulation properties, curd firmness modeling and acidity in milk from Brown Swiss cows. Animal : an international journal of animal bioscience 2015 Jul 9 (7): 1104-12. Cecchinato A, Chessa S, Ribeca C, Cipolat-Gotet C, Bobbo T, Casellas J, Bittante |
Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism. Clinical endocrinology 2015 1 82 (6): 876-84. Fritez Nabila, Sobrier Marie-Laure, Iraqi Hinde, Vié-Luton Marie-Pierre, Netchine Irène, El Annas Abdessamad, Pantel Jacques, Collot Nathalie, Rose Sophie, Piterboth William, Legendre Marie, Chraibi Abdelmjid, Amselem Serge, Kadiri Abdelkrim, Hilal Lati |
Pleiotropic Genes Affecting Carcass Traits in Bos indicus (Nellore) Cattle Are Modulators of Growth. PloS one 2016 11 (7): e0158165. G T Pereira Anirene, Utsunomiya Yuri T, Milanesi Marco, Torrecilha Rafaela B P, Carmo Adriana S, Neves Haroldo H R, Carvalheiro Roberto, Ajmone-Marsan Paolo, Sonstegard Tad S, Sölkner Johann, Contreras-Castillo Carmen J, Garcia José |
Pathogenic and likely pathogenic genetic alterations and polymorphisms in growth hormone gene (GH1) and growth hormone releasing hormone receptor gene (GHRHR) in a cohort of isolated growth hormone deficient (IGHD) children in Sri Lanka. Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 2017 Sep 36 22-29. Sundralingam Tharmini, Tennekoon Kamani Hemamala, de Silva Shamya, De Silva Sumadee, Hewage Asanka Sudeshi |
Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature. Endocrine journal 2017 8 64 (10): 947-954. Hattori Atsushi, Katoh-Fukui Yuko, Nakamura Akie, Matsubara Keiko, Kamimaki Tsutomu, Tanaka Hiroyuki, Dateki Sumito, Adachi Masanori, Muroya Koji, Yoshida Shinobu, Ida Shinobu, Mitani Marie, Nagasaki Keisuke, Ogata Tsutomu, Suzuki Erina, Hata Kenichiro, Nakabayashi Kazuhiko, Matsubara Yoichi, Narumi Satoshi, Tanaka Toshiaki, Fukami Ma |
Genetic determinants of growth hormone and GH-related phenotypes. BMC genomics 2017 Oct 18 (1): 822. Hallengren Erik, Almgren Peter, Svensson Malin, Gallo Widet, Engström Gunnar, Persson Margaretha, Melander Ol |
Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism. Molecular genetics & genomic medicine 2018 5 6 (4): 514-25. Pérez Millán María I, Vishnopolska Sebastian A, Daly Alexandre Z, Bustamante Juan P, Seilicovich Adriana, Bergadá Ignacio, Braslavsky Débora, Keselman Ana C, Lemons Rosemary M, Mortensen Amanda H, Marti Marcelo A, Camper Sally A, Kitzman Jacob |
Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity. Pituitary 2020 9 23 (6): 701-715. Kale Shantanu, Gada Jugal V, Jadhav Swati, Lila Anurag R, Sarathi Vijaya, Budyal Sweta, Patt Hiren, Goroshi Manjunath R, Thadani Puja M, Arya Sneha, Kamble Aparna A, Patil Virendra A, Acharya Shrikrishna, Sankhe Shilpa, Shivane Vyankatesh, Raghavan Vijaya, Bandgar Tushar R, Shah Nalini |
Variants in FtsJ RNA 2'-O-Methyltransferase 3 and Growth Hormone 1 are associated with small body size and a dental anomaly in dogs. Proceedings of the National Academy of Sciences of the United States of America 2020 9 117 (40): 24929-24935. Abrams Sydney R, Hawks Alexandra L, Evans Jacquelyn M, Famula Thomas R, Mahaffey Mary, Johnson Gary S, Mason Jennifer M, Clark Leigh An |
Polymorphism of the growth hormone gene GH1 in Polish children and adolescents with short stature. Endocrine 2020 Apr . Majewska Katarzyna Anna, Kedzia Andrzej, Kontowicz Przemyslaw, Prauzinska Magdalena, Szydlowski Jaroslaw, Switonski Marek, Nowacka-Woszuk Joan |
A patient with combined pituitary hormone deficiency and osteogenesis imperfecta associated with mutations in LHX4 and COL1A2. Journal of advanced research 2020 2 21 121-127. Hemwong Nalinee, Phokaew Chureerat, Srichomthong Chalurmpon, Tongkobpetch Siraprapa, Srilanchakon Khomsak, Supornsilchai Vichit, Suphapeetiporn Kanya, Porntaveetus Thantrira, Shotelersuk Voras |
Molecular characterization and analysis of the association of growth hormone 1 gene with growth traits in Chinese indigenous yak (Bos grunniens). Tropical animal health and production 2021 Mar 53 (2): 221. Gui Linsheng, Raza Sayed Haidar Abbas, Sun Yonggang, Sabek Ahmed, Abbas Sayed Qaisar, Shah Mujahid Ali, Khan Rajwali, Abdelnour Sameh |
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. European journal of endocrinology 2022 10 187 (6): 787-795. Fourneaux Rachel, Reynaud Rachel, Mougel Gregory, Castets Sarah, Bretones Patricia, Dauriat Benjamin, Edouard Thomas, Raverot Gerald, Barlier Anne, Brue Thierry, Castinetti Frederic, Saveanu Alexand |
Clinical and genetic evaluation of children with short stature of unknown origin. BMC medical genomics 2023 8 16 (1): 194. Qianqian Zhao, Yanying Li, Qian Shao, Chuanpeng Zhang, Shuang Kou, Wanling Yang, Mei Zhang, Bo B |
[A prospective study of genetic screening of 2 060 neonates by high-throughput sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 5 40 (6): 641-647. Danyan Zhuang, Fei Wang, Shuxia Ding, Zhoushu Zheng, Qi Yu, Lanqiu Lyu, Shuni Sun, Rulai Yang, Wenwen Que, Haibo |
Distribution of CMV envelope glycoprotein B, H and N genotypes in infants with congenital cytomegalovirus symptomatic infection. Frontiers in pediatrics 2023 4 11 1112645. Dong Niuniu, Cao Lingfeng, Zheng Danni, Su Liyun, Lu Lijuan, Dong Zuoquan, Xu Menghua, Xu J |
Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes. Archives of endocrinology and metabolism 2023 11 68 e220254. Tar?k K?rkgöz, Semra Gürsoy, Sezer Acar, Özlem Nalbanto?lu, Beyhan Özkaya, Hüseyin An?l Korkmaz, Filiz Hazan, Behzat Özk |
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