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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 - 8 (of 8 Records)

Query Trace: Disease and CHD4[original query]
Characteristics of genomic alterations of lung adenocarcinoma in young never-smokers.
International journal of cancer 2018 4 143 (7): 1696-1705.
Luo Wenxin, Tian Panwen, Wang Yue, Xu Heng, Chen Lu, Tang Chao, Shu Yang, Zhang Shouyue, Wang Zhoufeng, Zhang Jun, Zhang Li, Jiang Lili, Liu Lunxu, Che Guowei, Guo Chenglin, Zhang Hong, Wang Jiali, Li Weim
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Nature genetics 2018 12 51 (1): 106-116.
Coe Bradley P, Stessman Holly A F, Sulovari Arvis, Geisheker Madeleine R, Bakken Trygve E, Lake Allison M, Dougherty Joseph D, Lein Ed S, Hormozdiari Fereydoun, Bernier Raphael A, Eichler Evan
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy.
Genetics in medicine : official journal of the American College of Medical Genetics 2019 9 22 (2): 427-431.
Pinard Amélie, Guey Stéphanie, Guo Dongchuan, Cecchi Alana C, Kharas Natasha, Wallace Stephanie, Regalado Ellen S, Hostetler Ellen M, Sharrief Anjail Z, Bergametti Françoise, Kossorotoff Manoelle, Hervé Dominique, Kraemer Markus, Bamshad Michael J, Nickerson Deborah A, Smith Edward R, Tournier-Lasserve Elisabeth, Milewicz Dianna
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania.
BMC medical genetics 2020 Jun 21 (1): 125.
Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul
De novo damaging variants associated with congenital heart diseases contribute to the connectome.
Scientific reports 2020 Apr 10 (1): 7046.
Ji Weizhen, Ferdman Dina, Copel Joshua, Scheinost Dustin, Shabanova Veronika, Brueckner Martina, Khokha Mustafa K, Ment Laura
De novo variants in exomes of congenital heart disease patients identify risk genes and pathways.
Genome medicine 2020 1 12 (1): 9.
Sevim Bayrak Cigdem, Zhang Peng, Tristani-Firouzi Martin, Gelb Bruce D, Itan Yuv
Whole-exome sequencing reveals a comprehensive germline mutation landscape and identifies twelve novel predisposition genes in Chinese prostate cancer patients.
PLoS genetics 2022 Sep 18 (9): e1010373.
Liang Yonghao, Chiu Peter Ka-Fung, Zhu Yao, Wong Christine Yim-Ping, Xiong Qing, Wang Lin, Teoh Jeremy Yuen-Chun, Cao Qin, Wei Yu, Ye Ding-Wei, Tsui Stephen Kwok-Wing, Ng Chi-F
Clear Cell Adenocarcinoma of Urethra: Clinical and Pathologic Implications and Characterization of Molecular Aberrations.
Cancer research and treatment 2023 9 .
Boram Song, Seok Hyun Lee, Jeong Hwan Park, Kyung Chul Mo
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