Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.
American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01
Variant appearance in text: KDR: A772V; rs199982402
Genomic Alterations Identification and Resistance Mechanisms Exploration of NSCLC With Central Nervous System Metastases Using Liquid Biopsy of Cerebrospinal Fluid: A Real-World Study.
Frontiers In Oncology
Shen, Fangfang F; Liang, Naixin N; Fan, Zaiwen Z; Zhao, Min M; Kang, Jing J; Wang, Xifang X; Hu, Qun Q; Mu, Yongping Y; Wang, Kai K; Yuan, Mingming M; Chen, Rongrong R; Guo, Wei W; Dong, Guilan G; Zhao, Jun J; Bai, Jun J
Clinical genomic profiling in the management of patients with soft tissue and bone sarcoma.
Nature Communications
Gounder, Mrinal M MM; Agaram, Narasimhan P NP; Trabucco, Sally E SE; Robinson, Victoria V; Ferraro, Richard A RA; Millis, Sherri Z SZ; Krishnan, Anita A; Lee, Jessica J; Attia, Steven S; Abida, Wassim W; Drilon, Alexander A; Chi, Ping P; Angelo, Sandra P D' SP; Dickson, Mark A MA; Keohan, Mary Lou ML; Kelly, Ciara M CM; Agulnik, Mark M; Chawla, Sant P SP; Choy, Edwin E; Chugh, Rashmi R; Meyer, Christian F CF; Myer, Parvathi A PA; Moore, Jessica L JL; Okimoto, Ross A RA; Pollock, Raphael E RE; Ravi, Vinod V; Singh, Arun S AS; Somaiah, Neeta N; Wagner, Andrew J AJ; Healey, John H JH; Frampton, Garrett M GM; Venstrom, Jeffrey M JM; Ross, Jeffrey S JS; Ladanyi, Marc M; Singer, Samuel S; Brennan, Murray F MF; Schwartz, Gary K GK; Lazar, Alexander J AJ; Thomas, David M DM; Maki, Robert G RG; Tap, William D WD; Ali, Siraj M SM; Jin, Dexter X DX
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Škorić-Milosavljević, Doris D; Lahrouchi, Najim N; Bosada, Fernanda M FM; Dombrowsky, Gregor G; Williams, Simon G SG; Lesurf, Robert R; Tjong, Fleur V Y FVY; Walsh, Roddy R; El Bouchikhi, Ihssane I; Breckpot, Jeroen J; Audain, Enrique E; Ilgun, Aho A; Beekman, Leander L; Ratbi, Ilham I; Strong, Alanna A; Muenke, Maximilian M; Heide, Solveig S; Muir, Alison M AM; Hababa, Mariam M; Cross, Laura L; Zhou, Dihong D; Pastinen, Tomi T; , ; Zackai, Elaine E; Atmani, Samir S; Ouldim, Karim K; Adadi, Najlae N; Steindl, Katharina K; Rauch, Anita A; Brook, David D; Wilsdon, Anna A; Kuipers, Irene I; Blom, Nico A NA; Mulder, Barbara J BJ; Mefford, Heather C HC; Keren, Boris B; Joset, Pascal P; Kruszka, Paul P; Thiffault, Isabelle I; Sheppard, Sarah E SE; Roberts, Amy A; Lodder, Elisabeth M EM; Keavney, Bernard D BD; Clur, Sally-Ann B SB; Mital, Seema S; Hitz, Marc-Philip MP; Christoffels, Vincent M VM; Postma, Alex V AV; Bezzina, Connie R CR
Publication Date: 2021-10
Variant appearance in text: KDR: 2315C>T; Ala772Val
Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer.
Frontiers In Genetics
Glentis, Stavros S; Dimopoulos, Alexandros C AC; Rouskas, Konstantinos K; Ntritsos, George G; Evangelou, Evangelos E; Narod, Steven A SA; Mes-Masson, Anne-Marie AM; Foulkes, William D WD; Rivera, Barbara B; Tonin, Patricia N PN; Ragoussis, Jiannis J; Dimas, Antigone S AS
Publication Date: 2019
Variant appearance in text: KDR: A772V; rs199982402
A Landscape of Pharmacogenomic Interactions in Cancer.
Cell
Iorio, Francesco F; Knijnenburg, Theo A TA; Vis, Daniel J DJ; Bignell, Graham R GR; Menden, Michael P MP; Schubert, Michael M; Aben, Nanne N; Gonçalves, Emanuel E; Barthorpe, Syd S; Lightfoot, Howard H; Cokelaer, Thomas T; Greninger, Patricia P; van Dyk, Ewald E; Chang, Han H; de Silva, Heshani H; Heyn, Holger H; Deng, Xianming X; Egan, Regina K RK; Liu, Qingsong Q; Mironenko, Tatiana T; Mitropoulos, Xeni X; Richardson, Laura L; Wang, Jinhua J; Zhang, Tinghu T; Moran, Sebastian S; Sayols, Sergi S; Soleimani, Maryam M; Tamborero, David D; Lopez-Bigas, Nuria N; Ross-Macdonald, Petra P; Esteller, Manel M; Gray, Nathanael S NS; Haber, Daniel A DA; Stratton, Michael R MR; Benes, Cyril H CH; Wessels, Lodewyk F A LFA; Saez-Rodriguez, Julio J; McDermott, Ultan U; Garnett, Mathew J MJ
Subclonal diversification of primary breast cancer revealed by multiregion sequencing.
Nature Medicine
Yates, Lucy R LR; Gerstung, Moritz M; Knappskog, Stian S; Desmedt, Christine C; Gundem, Gunes G; Van Loo, Peter P; Aas, Turid T; Alexandrov, Ludmil B LB; Larsimont, Denis D; Davies, Helen H; Li, Yilong Y; Ju, Young Seok YS; Ramakrishna, Manasa M; Haugland, Hans Kristian HK; Lilleng, Peer Kaare PK; Nik-Zainal, Serena S; McLaren, Stuart S; Butler, Adam A; Martin, Sancha S; Glodzik, Dominic D; Menzies, Andrew A; Raine, Keiran K; Hinton, Jonathan J; Jones, David D; Mudie, Laura J LJ; Jiang, Bing B; Vincent, Delphine D; Greene-Colozzi, April A; Adnet, Pierre-Yves PY; Fatima, Aquila A; Maetens, Marion M; Ignatiadis, Michail M; Stratton, Michael R MR; Sotiriou, Christos C; Richardson, Andrea L AL; Lønning, Per Eystein PE; Wedge, David C DC; Campbell, Peter J PJ