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You searched for: Author Chung, Wendy K. Subject Genetics Start Over

1. Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study

Griffin, Emily Leann; Nees, Shannon N.; Morton, Sarah U.; Wynn, Julia; Patel, Nihir; Jobanputra, Vaidehi; Robinson, Scott; Kochav, Stephanie M.; Tao, Alice May; Andrews, Carli; Cross, Nancy; Geva, Judith; Lanzilotta, Kristen; Ritter, Alyssa; Taillie, Eileen; Thompson, Alexandra; Meyer, Chris; Akers, Rachel; King, Eileen C.; Cnota, James F.; Kim, Richard W.; Porter, Jr., George A.; Brueckner, Martina; Seidman, Christine E.; Shen, Yufeng; Gelb, Bruce D.; Goldmuntz, Elizabeth; Newburger, Jane W.; Roberts, Amy E.; Chung, Wendy K.
2023
Articles
Congenital heart diseaseGeneticsGenetic screeningMedicine

4. Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterized by extreme morbidity and mortality

Machado, Rajiv D.; Welch, Carrie L.; Haimel, Matthias; Bleda, Marta; Colglazier, Elizabeth; Coulson, John D.; Debeljak, Marusa; Ekstein, Josef; Fineman, Jeffrey R.; Golden, William Christopher; Griffin, Emily Leann; Hadinnapola, Charaka; Harris, Michael A.; Hirsch, Yoel; Hoover-Fong, Julie Elizabeth; Nogee, Lawrence; Romer, Lewis H.; Vesel, Samo; Gräf, Stefan; Morrell, Nicholas W.; Southgate, Laura; Chung, Wendy K.; NIHR Bioresource – Rare Diseases
2021
Articles
GeneticsPediatricsCor pulmonale

5. Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Zhu, Na; Swietlik, Emilia M.; Welch, Carrie L.; Pauciulo, Michael W.; Hagen, Jacob J.; Zhou, Xueya; Guo, Yicheng; Karten, Johannes; Pandya, Divya; Tilly, Tobias; Lutz, Katie A.; Martin, Jennifer M.; Treacy, Carmen M.; Rosenzweig, Erika B.; Krishnan, Usha; Coleman, Anna W.; Gonzaga-Juaregui, Claudia; Lawrie, Allan; Trembath, Richard C.; Wilkins, Martin R.; Morrell, Nicholas W.; Shen, Yufeng; Gräf, Stefan; Nichols, William C.; Chung, Wendy K.
2021
Articles
GeneticsLungs--DiseasesHypertensionClinical trials

6. Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC)

Zeinomar, Nur; Knight, Julia A.; Genkinger, Jeanine M.; Phillips, Kelly-Anne; Daly, Mary B.; Milne, Roger L.; Dite, Gillian S.; Kehm, Rebecca D.; Liao, Yuyan; Southey, Melissa C.; Chung, Wendy K.; Giles, Graham G.; McLachlan, Sue-Anne; Friedlander, Michael L.; Weideman, Prue C.; Glendon, Gord; Nesci, Stephanie; Andrulis, Irene L.; Buys, Saundra S.; John, Esther M.; MacInnis, Robert J.; Hopper, John L.; Terry, Mary B.
2019
Articles
Breast--CancerDrinking of alcoholic beveragesSmokingGenetics

8. Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

Kehm, Rebecca D.; Hopper, John L.; John, Esther M.; Phillips, Kelly-Anne; MacInnis, Robert J.; Dite, Gillian S.; Milne, Roger L.; Liao, Yuyan; Zeinomar, Nur; Knight, Julia A.; Southey, Melissa C.; Vahdat, Linda; Kornhauser, Naomi; Cigler, Tessa; Chung, Wendy K.; Giles, Graham G.; McLachlan, Sue-Anne; Friedlander, Michael L.; Weideman, Prue C.; Glendon, Gord; Nesci, Stephanie; Andrulis, Irene L.; Buys, Saundra S.; Daly, Mary B.; Terry, Mary B.
2019
Articles
Breast--CancerNonsteroidal anti-inflammatory agentsFamily historiesGenetics

9. Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease

Zhu, Na; Welch, Carrie L.; Wang, Jiayao; Allen, Philip M.; Gonzaga-Jauregui, Claudia; Ma, Lijiang; King, Alejandra K.; Krishnan, Usha; Rosenzweig, Erika B.; Ivy, D. Dunbar; Austin, Eric D.; Hamid, Rizwan; Pauciulo, Michael W.; Lutz, Katie A.; Nichols, William C.; Reid, Jeffrey G.; Overton, John D.; Baras, Aris; Dewey, Frederick E.; Shen, Yufeng; Chung, Wendy K.
2018
Articles
Pulmonary hypertensionCongenital heart diseaseExomesGeneticsGenomics

10. The Congenital Heart Disease Genetic Network Study: Cohort description

Hoang, Thanh T.; Goldmuntz, Elizabeth; Roberts, Amy E.; Chung, Wendy K.; Kline, Jennie K; Deanfield, John E.; Giardini, Alessandro; Aleman, Adolfo; Gelb, Bruce D.; Neal, Meghan Mac; Porter, Jr., George A.; Kim, Richard; Brueckner, Martina; Lifton, Richard P.; Edman, Sharon; Woyciechowski, Stacy; Mitchel, Laura E.; Agopian, A. J.
2018
Articles
Congenital heart diseasePediatricsGeneticsEpidemiology

11. Loss of RNA expression and allele-specific expression associated with congenital heart disease

McKean, David M.; Homsy, Jason; Wakimoto, Hiroko; Patel, Neil; Ware, James S.; DePalma, Steven R.; Gorham, Joshua; Zaidi, Samir; Ma, Wenji; Patel, Nihir; Shen, Yufeng; Chung, Wendy K.; Lifton, Richard P.; Kim, Richard; Brueckner, Martina; Goldmuntz, Elizabeth; Sharp, Andrew J.; Seidman, Christine E.; Gelb, Bruce D.; Seidman, J. G.
2016
Articles
Gene expressionAbnormalities, HumanRNACongenital heart diseaseGenetics

15. Use of Genetic Tests among Neurologists and Psychiatrists: Knowledge, Attitudes, Behaviors, and Needs for Training

Salm, Melissa; Abbate, Kristopher J.; Appelbaum, Paul S.; Ottman, Ruth; Chung, Wendy K.; Marder, Karen; Leu, Cheng Shiun; Alcalay, Roy Nissim; Goldman, Jill; Curtis, Alexander Malik; Leech, Christopher; Taber, Katherine Johansen; Klitzman, Robert L.
2014
Articles
GeneticsHuman chromosome abnormalities--DiagnosisGenetic counselingNeurologistsPsychiatristsPhysicians--AttitudesBioethics

19. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Mulligan, Anna; Couch, Fergus; Barrowdale, Daniel; Domchek, Susan; Eccles, Diana; Nevanlinna, Heli; Ramus, Susan; Robson, Mark; Sherman, Mark; Spurdle, Amanda; Wappenschmidt, Barbara; Lee, Andrew; McGuffog, Lesley; Healey, Sue; Sinilnikova, Olga; Janavicius, Ramunas; Hansen, Thomas; Nielsen, Finn; Ejlertsen, Bent; Osorio, Ana; Muñoz-Repeto, Ivan; Duran, Mercedes; Godino, Javier; Pertesi, Maroulio; Benítez, Javier; Peterlongo, Paolo; Manoukian, Siranoush; Peissel, Bernard; Zaffaroni, Daniela; Cattaneo, Elisa; Bonanni, Bernardo; Viel, Alessandra; Pasini, Barbara; Papi, Laura; Ottini, Laura; Savarese, Antonella; Bernard, Loris; Radice, Paolo; Hamann, Ute; Verheus, Martijn; Meijers-Heijboer, Hanne; Wijnen, Juul; Gómez García, Encarna; Nelen, Marcel; Kets, C Marleen; Seynaeve, Caroline; Tilanus-Linthorst, Madeleine; van der Luijt, Rob; Os, Theo; Rookus, Matti; Frost, Debra; Jones, J. Louise; Evans, D. Gareth; Lalloo, Fiona; Eeles, Ros; Izatt, Louise; Adlard, Julian; Davidson, Rosemarie; Cook, Jackie; Donaldson, Alan; Dorkins, Huw; Gregory, Helen; Eason, Jacqueline; Houghton, Catherine; Barwell, Julian; Side, Lucy; McCann, Emma; Murray, Alex; Peock, Susan; Godwin, Andrew; Schmutzler, Rita; Rhiem, Kerstin; Engel, Christoph; Meindl, Alfons; Ruehl, Ina; Arnold, Norbert; Niederacher, Dieter; Sutter, Christian; Deissler, Helmut; Gadzicki, Dorothea; Kast, Karin; Preisler-Adams, Sabine; Varon-Mateeva, Raymonda; Schoenbuchner, Ines; Fiebig, Britta; Heinritz, Wolfram; Schäfer, Dieter; Gevensleben, Heidrun; Caux-Moncoutier, Virginie; Fassy-Colcombet, Marion; Cornelis, François; Mazoyer, Sylvie; Léoné, Mélanie; Boutry-Kryza, Nadia; Hardouin, Agnès; Berthet, Pascaline; Muller, Danièle; Fricker, Jean-Pierre; Mortemousque, Isabelle; Pujol, Pascal; Coupier, Isabelle; Lebrun, Marine; Kientz, Caroline; Longy, Michel; Sevenet, Nicolas; Stoppa-Lyonnet, Dominique; Isaacs, Claudine; Caldes, Trinidad; de la Hoya, Miguel; Heikkinen, Tuomas; Aittomäki, Kristiina; Blanco, Ignacio; Lazaro, Conxi; Barkardottir, Rosa; Soucy, Penny; Dumont, Martine; Simard, Jacques; Montagna, Marco; Tognazzo, Silvia; D'Andrea, Emma; Fox, Stephen; Yan, Max; Rebbeck, Tim; Olopade, Olufunmilayo; Weitzel, Jeffrey; Lynch, Henry; Ganz, Patricia; Tomlinson, Gail; Wang, Xianshu; Fredericksen, Zachary; Pankratz, Vernon; Lindor, Noralane; Szabo, Csilla; Offit, Kenneth; Sakr, Rita; Gaudet, Mia; Bhatia, Jasmine; Kauff, Noah; Singer, Christian; Tea, Muy-Kheng; Gschwantler-Kaulich, Daphne; Fink-Retter, Anneliese; Mai, Phuong; Greene, Mark; Imyanitov, Evgeny; O'Malley, Frances; Ozcelik, Hilmi; Glendon, Gordon; Toland, Amanda; Gerdes, Anne-Marie; Thomassen, Mads; Kruse, Torben; Jensen, Uffe; Skytte, Anne-Bine; Caligo, Maria; Soller, Maria; Henriksson, Karin; Wachenfeldt, von Anna; Arver, Brita; Stenmark-Askmalm, Marie; Karlsson, Per; Ding, Yuan; Neuhausen, Susan; Beattie, Mary; Pharoah, Paul; Moysich, Kirsten; Nathanson, Katherine; Karlan, Beth; Gross, Jenny; John, Esther; Daly, Mary; Buys, Saundra; Southey, Melissa; Hopper, John; Terry, Mary Beth; Chung, Wendy K.; Miron, Alexander; Goldgar, David; Chenevix-Trench, Georgia; Easton, Douglas; Andrulis, Irene; Antoniou, Antonis
2011
Articles
Mutation (Biology)Breast--CancerGeneticsMolecular biology