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Showing results 1 to 6 of 6

	Title	Author(s)	Issue Date	Views
	DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes Journal:The American Journal of Human Genetics	Choufani, S Gibson, WT Turinsky, AL Chung, BHY Wang, T Garg, K Vitriolo, A Cohen, ASA Cyrus, S Goodman, S Chater-Diehl, E Brzezinski, J Brudno, M Luk, HM White, SM Lynch, SA Clericuzio, C Temple, IK Flinter, F MdConnell, V Cushing, T Bird, LM Splitt, M Kerr, B Scherer, SW Machado, J Imagawa, E Okamoto, N Matsumoto, N Testa, G Iascone, M Tenconi, R Caluseriu, O Mendoza-Londono, R Chitayat, D Cytrynabum, C Tatton-Brown, K Weksberg, R	2020	48
	EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome Journal:Journal of Translational Genetics and Genomics	Goodman, SJ Cytrynbaum, C Chung, BHY Chater-Diehl, E Aziz, C Turinsky, AL Kellam, B Keller, M Ko, JM Caluseriu, O Grafodatskaya, D McCready, E Perrier, R Yeung, KS Luk, HM Machado, J Brudno, M Stavropoulos, DJ Scherer, SW Innes, AM Cheung, SW Choufani, S Weksberg, R	2020	46
	GA4GH: International policies and standards for data sharing across genomic research and healthcare Journal:Cell Genomics	Rehm, HL Page, A Smith, L Adams, J Alterovitz, G Babb, LJ Barkley, MP Baudis, M Beauvais, MJS Beck, T Beckmann, JS Beltran, S Bernick, D Bernier, A Bonfield, JK Boughtwood, TF Bourque, G Bowers, SR Brookes, AJ Brudno, M Brush, MH Bujold, D Burdett, T Buske, OJ Cabill, MN Cameron, DL Carroll, RJ Cases-Silva, E Chakravarty, D Chaudhari, BP Chen, SH Cherry, JM Chung, J Cline, M Clissold, HL Cook-Deegan, RM Courtot, M Cunningham, F Cupak, M Davies, RM Denisko, D Doerr, MJ Dolman, LI Dove, ES Dursi, JL Dyke, SOM Eddy, JA Ellbeck, K Ellrott, KP Fairley, S Fakhro, KA Firth, HV Fitzsimons, MS Flume, M Flicek, P Fore, IM Freeberg, MA Freimuth, RR Fromont, LA Fuerth, J Gaff, CL Gan, W Ghanaim, EM Glazer, D Green, RC Griffith, M Griffith, OL Grossman, RL Groza, T Guldry Auvil, JM Gulgo, R Gupta, D Haendel, MA Hamosh, A Hansen, DP Hart, RK Hartley, DM Haussler, D Hendricks-Sturrup, RM Ho, WLC Hobb, AE Hoffman, MM Hofmann, OM Holub, P Hsu, JS Hubaux, JP Hunt, SE Husami, A Jacobsen, JO Jamuar, SS Janes, EL Jeanson, F Jene, A Johns, AL Joly, Y Jones, SJM Kanitz, A Kato, K Keane, TM Kekesi-Lafrance, K Kelleher, J Kerry, G Khor, SS Knoppers, BM Konopko, MA Kosaki, K Kuba, M Lawson, J Leinonen, R Li, S Lin, MF Linden, M Liu, X Llyanage, IU Lopez, J Lucassen, AM Lukowski, M Mann, AL Marshall, J Mattoni, M Melke-Jimenez, A Middleton, A Milne, RJ Molnar-Gabor, F Mulder, N Munoz-Torres, MC Nag, R Nakagawa, H Nasir, J Navarro, A Nelson, TH Niewielska, A Nisselle, A Niu, J Nyronen, TH O'Connor, BD Oesterie, S Ogishima, S Ota Wang, V Paglione, LAD Palumbo, E Parkinson, HE Philippakis, AA Pizarro, AD Prlic, A Rambla, J Rendon, A Rider, RA Robinson, PN Rodamer, KW Rodriguez, LL Rubin, AF Rueda, M Rushton, GA Ryan, RS Saunders, GI Schuilenburg, H Schwede, T Scollen, S Senf, A Sheffield, NC Skantharajah, N Smith, AV Sofia, HJ Spalding, D Spurdle, AB Stark, Z Stein, LD Suematsu, M Tan, P Tedds, JA Thomson, AA Thorogood, A Tickle, TL Tokunaga, K Tomroos, J Torrents, D Upchurch, S Valencia, A Guimera, RV Vamathevan, J Varma, S Vears, DF Viner, C Voisin, C Wagner, AH Wallace, SE Walsh, BP Williams, MS Winkler, EC Wold, BJ Wood, GM Woolley, JP Yamasaki, C Yates, AD Yung, CK Zass, LJ Zaytseva, K Zhang, J Goodhand, P North, K Birney, E	2021	7
	NSD1 mutations generate a genome-wide DNA methylation signature Journal:Nature Communications	Choufani, S Cytrynbaum, C Chung, BHY Turinsky, AL Grafodatskaya, D Chen, YA Cohen, ASA Dupuis, L Butcher, DT Siu, MT Luk, HM Lo, IFM Lam, STS Caluseriu, O Stavropoulos, DJ Reardon, W Mendoza-Londono, R Brudno, M Gibson, WT Chitayat, D	2015	72
	NSD1+/- DNA methylation (DNAm) signature: A novel functional diagnostic tool for Sotos syndrome Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014	Chonufani, S Cytrynbaum, C Chung, BHY Turinsky, AL Grafodatskaya, D Chen, YA Luk, HM Lo, IFM Lam, STS Stavropoulos, DJ Gibson, B Reardon, M Brudno, M Mendoza-Londono, R Chitayat, D Weksberg, R	2014	62
	A specific DNA methylation signature associated with NSD1+/- mutations in Sotos syndrome reveals a significant genome-wide loss of DNA methylation (DNAm) targeting CGs in regulatory regions of key developmental genes Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Choufani, S Cytrynbaum, C Turinsky, AL Chen, YA Grafodatskaya, D Xiang, J Feigenberg, M Chung, BHY Stavropoulos, DJ Mendoza-Londono, R Chitayat, D Gibson, WT Reardon, M Brudno, M Weksberg, R	2013	42

Showing results 1 to 6 of 6