Results 91 to 100 of about 2,604 (176)
Risk of carcinomas among children and adolescents with birth defects. [PDF]
Cancer EpidemiolSchraw JM, Tark JY, Desrosiers TA, Chambers TM, Shumate CJ, Nembhard WN, Yazdy MM, Nestoridi E, Malone MFW, Laetsch TW, Widemann BC, Janitz AE, Tanner JP, Kirby RS, Salemi JL, Spector LG, Huff CD, Plon SE, Lupo PJ. +18 moreeuropepmc +1 more sourceCalibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria. [PDF]
Genet MedBergquist T, Stenton SL, Nadeau EAW, Byrne AB, Greenblatt MS, Harrison SM, Tavtigian SV, O'Donnell-Luria A, Biesecker LG, Radivojac P, Brenner SE, Pejaver V, ClinGen Sequence Variant Interpretation Working Group. +12 moreeuropepmc +1 more sourceCo-occurrence of congenital anomalies and childhood brain tumors in 22 million live births. [PDF]
Neuro OncolHoang TT, Schraw JM, Shumate C, Desrosiers TA, Nembhard WN, Yazdy M, Nestoridi E, Janitz AE, Kirby RS, Salemi JL, Tanner JP, Chambers TM, Taylor MD, Huff CD, Plon SE, Lupo PJ, Scheurer ME. +16 moreeuropepmc +1 more sourceA quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndrome. [PDF]
Genome MedFortuno C, Frone MN, Mester J, de la Hoya M, Mai PL, Pesaran T, Achatz MI, Bassett R, Bustamante C, Crowley S, de Andrade KC, Evans DG, Feng B, Fuqua L, Harrell MI, Hatton JN, Huether R, Kesserwan C, Lee K, MacFarland SP, Maciaszek JL, Maxwell K, McGoldrick K, Murphy M, Nehoray B, Penkert J, Pinto EM, Plon SE, Schwartz-Levine A, Thompson AS, Wang W, Zambetti GP, Zelley K, James PA, Savage SA, Kratz CP, Spurdle AB. +36 moreeuropepmc +1 more sourceMondo: integrating disease terminology across communities. [PDF]
GeneticsVasilevsky NA, Toro S, Matentzoglu N, Flack JE, Mullen KR, Hegde H, Gehrke S, Whetzel PL, Shwetar Y, Harris NL, Ngu MS, Alyea GL, Kane MS, Roncaglia P, Sid E, Thaxton CL, Wood V, Abraham RS, Achatz MI, Ajuyah P, Amberger JS, Babb L, Baker J, Balhoff JP, Berg JS, Bhalla A, Bofill-De Ros X, Braun IR, Broeren EC, Byer BK, Byrne AB, Callahan TJ, Carmody LC, Chan LE, Clause AR, Cohen JS, DeLuca M, Deuitch NT, Flowers M, Fraser J, Fujiwara T, Gitau V, Goldstein JL, Gration D, Groza T, Gyori BM, Hankey W, Hilton JA, Himmelstein DS, Hong SS, Hoyt CT, Huether R, Hurwitz E, Jacobsen JOB, Kikuchi A, Köhler S, Korn DR, Lagorce D, Laraway BJ, Li JY, Malheiro AJ, McLaughlin J, Meldal BHM, Mohan S, Moxon SAT, Munoz-Torres MC, Nelson TH, Nicholas FW, Ochoa D, Olson D, Oprea TI, Oskotsky TT, Osumi-Sutherland D, Paris K, Parkinson HE, Pendlington ZM, Peng XP, Pizzino A, Plon SE, Powell BC, Ratliff JC, Rehm HL, Remennik L, Riggs ER, Roberts S, Robinson PN, Ross JE, Schaper K, Schilder BM, Schmidt JL, Sharp EW, Similuk MN, Smedley D, Sneddon TP, Sparks R, Stefancsik R, Stupp GS, Sundar S, Takatsuki T, Tammen I, Tshering KC, Unni DR, Valasek E, Vanderver A, Wagner AH, Webb RF, Welter D, Yaya-Stupp D, Zankl A, Zhang XA, McMurry JA, Chute CG, Hamosh A, Mungall CJ, Haendel MA. +114 moreeuropepmc +1 more sourceBeyond Mendel: a call to revisit the genotype-phenotype map through new experimental paradigms. [PDF]
GeneticsTautz D, Pallares LF, Andersson L, Barghi N, Barton N, Bay R, Chan YF, Hancock A, Kaiser TS, Koenig D, Kontarakis Z, Liedvogel M, de Meaux J, Nordborg M, Palmer AA, Purugganan M, Schlötterer C, Schmid K, Stainier DYR, Weigel D, Wolf JBW, Ebert D, Gibson G. +22 moreeuropepmc +1 more source
