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by Huang, Kuan-lin and Mashl, R. Jay and Wu, Yige and Wu, Ye and Ritter, Deborah I and Wang, Jiayin and Wang, Timothy and Wang, Liang-Bo and Wang, Jing and Wang, Zhining and Wang, Jioajiao and Wang, Chen and Wang, Linghua and Wang, Min and Oh, Clara and Paczkowska, Marta and Reynolds, Sheila and Wyczalkowski, Matthew A and Oak, Ninad and Scott, Adam D and Krassowski, Michal and Cherniack, Andrew D and Houlahan, Kathleen E and Jayasinghe, Reyka and Zhou, Wanding and Zhou, Daniel Cui and Liu, Xiuping and Liu, Jia and Liu, Wenbin and Liu, Yuexin and Liu, Di and Cao, Song and Kim, Jaegil and Kim, Tae-Beom and Kim, Young Won and Koire, Amanda and McMichael, Joshua F and Hucthagowder, Vishwanathan and Hahn, Abigail and McLellan, Michael D and Al-Mulla, Fahd and Johnson, Kimberly J and Caesar-Johnson, Samantha J and Demchok, John A and Felau, Ina and Kasapi, Melpomeni and Ferguson, Martin L and Hutter, Carolyn M and Sofia, Heidi J and Tarnuzzer, Roy and Yang, Ian and Yang, Ju Dong and Yang, Hannah and Yang, Liming and Zenklusen, Jean C and Zhang, Jiashan (Julia) and Zhang, Hailei and Zhang, Lizhi and Zhang, Hongzheng and Zhang, Wei and Zhang, Jiexin and Zhang, Hongxin and Chudamani, Sudha and Lolla, Laxmi and Naresh, Rashi and Pihl, Todd and Sun, Yichao and Sun, Qiang and Wan, Yunhu and Cho, Juok and DeFreitas, Timothy and Frazer, Scott and Gehlenborg, Nils and Getz, Gad and Heiman, David I and Lawrence, Michael S and Lin, Pei and Meier, Sam and Noble, Michael S and Saksena, Gordon and Voet, Doug and Bernard, Brady and Chambwe, Nyasha and Dhankani, Varsha and Knijnenburg, Theo and Kramer, Roger and Leinonen, Kalle and Miller, Michael and Miller, Judy and Miller, Christopher A and Shmulevich, Ilya and Thorsson, Vesteinn and Akbani, Rehan and Broom, Bradley M and Hegde, Apurva M and Ju, Zhenlin and Kanchi, Rupa S and Korkut, Anil and Li, Wei and Li, Jun and ... and Canc Genome Atlas Res Network and Cancer Genome Atlas Research Network
Cell, ISSN 0092-8674, 04/2018, Volume 173, Issue 2, pp. 355 - 370.e14
We conducted the largest investigation of predisposition variants in cancer to date, discovering 853 pathogenic or likely pathogenic variants in 8% of 10,389... 
cancer predisposition | LOH | variant pathogenicity | germline and somatic genomes | GENOMICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | KINASE | GUIDELINES | SITES | RISK | MUTATIONS | BRCA1 | DISCOVERY | CELL BIOLOGY | Cancer predisposition
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 5, pp. 478 - 481
Journal Article
TRENDS IN GENETICS, ISSN 0168-9525, 07/2019, Volume 35, Issue 7, pp. 515 - 526
Cancer is characterized by diverse genetic alterations in both germline and somatic genomes that disrupt normal biology and provide a selective advantage to... 
WIDE ASSOCIATION SCAN | POLYMORPHISMS | METAANALYSIS | ALLELE-SPECIFIC IMBALANCE | BREAST-CANCER RISK | MICROSATELLITE INSTABILITY | COLORECTAL-CANCER | GENETICS & HEREDITY | CARCINOMAS | SUSCEPTIBILITY GENE | MUTATIONS | Anopheles | Lubrication and lubricants | Analysis | Genes | Genomics | Amino acids | Disease susceptibility | Tumors
Journal Article
Pigment Cell & Melanoma Research, ISSN 1755-1471, 09/2019, Volume 32, Issue 5, pp. 734 - 738
Germline mutations in CDKN 2A (p16) are commonly found in patients with family history of melanoma or personal history of multiple primary melanomas. The p16... 
binding | melanoma | CDKN | AMP | germline | p16 | CDKN2A | PROTEIN-STRUCTURE | CELL BIOLOGY | DERMATOLOGY | INDIVIDUALS | AMP binding | ONCOLOGY | TUMOR-SUPPRESSOR | MUTATIONS | MELANOCYTIC NEVI | Genetic aspects | Melanoma
Journal Article
Human Mutation, ISSN 1059-7794, 12/2018, Volume 39, Issue 12, pp. 2025 - 2039
Journal Article