Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and LHX3[original query] |
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Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Nature communications 2015 6 8658. Artigas María Soler, Wain Louise V, Miller Suzanne, Kheirallah Abdul Kader, Huffman Jennifer E, Ntalla Ioanna, Shrine Nick, Obeidat Ma'en, Trochet Holly, McArdle Wendy L, Alves Alexessander Couto, Hui Jennie, Zhao Jing Hua, Joshi Peter K, Teumer Alexander, Albrecht Eva, Imboden Medea, Rawal Rajesh, Lopez Lorna M, Marten Jonathan, Enroth Stefan, Surakka Ida, Polasek Ozren, Lyytikäinen Leo-Pekka, Granell Raquel, Hysi Pirro G, Flexeder Claudia, Mahajan Anubha, Beilby John, Bossé Yohan, Brandsma Corry-Anke, Campbell Harry, Gieger Christian, Gläser Sven, González Juan R, Grallert Harald, Hammond Chris J, Harris Sarah E, Hartikainen Anna-Liisa, Heliövaara Markku, Henderson John, Hocking Lynne, Horikoshi Momoko, Hutri-Kähönen Nina, Ingelsson Erik, Johansson Åsa, Kemp John P, Kolcic Ivana, Kumar Ashish, Lind Lars, Melén Erik, Musk Arthur W, Navarro Pau, Nickle David C, Padmanabhan Sandosh, Raitakari Olli T, Ried Janina S, Ripatti Samuli, Schulz Holger, Scott Robert A, Sin Don D, Starr John M, , Viñuela Ana, Völzke Henry, Wild Sarah H, Wright Alan F, Zemunik Tatijana, Jarvis Deborah L, Spector Tim D, Evans David M, Lehtimäki Terho, Vitart Veronique, Kähönen Mika, Gyllensten Ulf, Rudan Igor, Deary Ian J, Karrasch Stefan, Probst-Hensch Nicole M, Heinrich Joachim, Stubbe Beate, Wilson James F, Wareham Nicholas J, James Alan L, Morris Andrew P, Jarvelin Marjo-Riitta, Hayward Caroline, Sayers Ian, Strachan David P, Hall Ian P, Tobin Martin |
| 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 |
| Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency. Endocrine 2019 May . Bajuk Studen Katica, Stefanija Magdalena Avbelj, Saveanu Alexandru, Barlier Anne, Brue Thierry, Pfeifer Mari |
| Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients. Frontiers in endocrinology 2021 9 12 711991. Yu Chenxi, Xie Bobo, Zhao Zhengye, Zhao Sen, Liu Lian, Cheng Xi, Li Xiaoxin, Cao Bingyan, Shao Jiashen, Chen Jiajia, Zhao Hengqiang, Yan Zihui, Su Chang, Niu Yuchen, Song Yanning, Wei Liya, Wang Yi, Ren Xiaoya, Fan Lijun, Zhang Beibei, Li Chuan, Gui Baoheng, Zhang Yuanqiang, Wang Lianlei, Chen Shaoke, Zhang Jianguo, Wu Zhihong, Gong Chunxiu, Fan Xin, Wu N |
| Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
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