Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association
Pierpont, Mary Ella, Brueckner, Martina, Chung, Wendy K, Garg, Vidu, Lacro, Ronald V, McGuire, Amy L, Mital, Seema, Priest, James R, Pu, William T, Roberts, Amy, Ware, Stephanie M, Gelb, Bruce D, Russell, Mark W
Published in Circulation (New York, N.Y.) (20.11.2018)
Published in Circulation (New York, N.Y.) (20.11.2018)
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Journal Article
Genetic Basis of Human Congenital Heart Disease
Nees, Shannon N, Chung, Wendy K
Published in Cold Spring Harbor perspectives in biology (01.09.2020)
Published in Cold Spring Harbor perspectives in biology (01.09.2020)
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ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
Miller, David T., Lee, Kristy, Chung, Wendy K., Gordon, Adam S., Herman, Gail E., Klein, Teri E., Stewart, Douglas R., Amendola, Laura M., Adelman, Kathy, Bale, Sherri J., Gollob, Michael H., Harrison, Steven M., Hershberger, Ray E., McKelvey, Kent, Richards, C. Sue, Vlangos, Christopher N., Watson, Michael S., Martin, Christa Lese
Published in Genetics in medicine (01.08.2021)
Published in Genetics in medicine (01.08.2021)
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MVP predicts the pathogenicity of missense variants by deep learning
Qi, Hongjian, Zhang, Haicang, Zhao, Yige, Chen, Chen, Long, John J., Chung, Wendy K., Guan, Yongtao, Shen, Yufeng
Published in Nature communications (21.01.2021)
Published in Nature communications (21.01.2021)
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Clinical application of whole-exome sequencing across clinical indications
Retterer, Kyle, Juusola, Jane, Cho, Megan T., Vitazka, Patrik, Millan, Francisca, Gibellini, Federica, Vertino-Bell, Annette, Smaoui, Nizar, Neidich, Julie, Monaghan, Kristin G., McKnight, Dianalee, Bai, Renkui, Suchy, Sharon, Friedman, Bethany, Tahiliani, Jackie, Pineda-Alvarez, Daniel, Richard, Gabriele, Brandt, Tracy, Haverfield, Eden, Chung, Wendy K., Bale, Sherri
Published in Genetics in medicine (01.07.2016)
Published in Genetics in medicine (01.07.2016)
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Artificial intelligence and the impact on medical genetics
Solomon, Benjamin D, Chung, Wendy K
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.09.2023)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.09.2023)
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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
Kalia, Sarah S., Adelman, Kathy, Bale, Sherri J., Chung, Wendy K., Eng, Christine, Evans, James P., Herman, Gail E., Hufnagel, Sophia B., Klein, Teri E., Korf, Bruce R., McKelvey, Kent D., Ormond, Kelly E., Richards, C. Sue, Vlangos, Christopher N., Watson, Michael, Martin, Christa L., Miller, David T.
Published in Genetics in medicine (01.02.2017)
Published in Genetics in medicine (01.02.2017)
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ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Miller, David T., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Gordon, Adam S., Harrison, Steven M., Hershberger, Ray E., Klein, Teri E., Richards, Carolyn Sue, Stewart, Douglas R., Martin, Christa Lese
Published in Genetics in medicine (01.07.2022)
Published in Genetics in medicine (01.07.2022)
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Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)
Chung, Wendy K, Erion, Karel, Florez, Jose C, Hattersley, Andrew T, Hivert, Marie-France, Lee, Christine G, McCarthy, Mark I, Nolan, John J, Norris, Jill M, Pearson, Ewan R, Philipson, Louis, McElvaine, Allison T, Cefalu, William T, Rich, Stephen S, Franks, Paul W
Published in Diabetes care (01.07.2020)
Published in Diabetes care (01.07.2020)
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Conference Proceeding
Genetics and Genomics of Pulmonary Arterial Hypertension
Soubrier, Florent, MD, PhD, Chung, Wendy K., MD, PhD, Machado, Rajiv, PhD, Grünig, Ekkehard, MD, Aldred, Micheala, PhD, Geraci, Mark, MD, Loyd, James E., MD, Elliott, C. Gregory, MD, Trembath, Richard C., MD, Newman, John H., MD, Humbert, Marc, MD, PhD
Published in Journal of the American College of Cardiology (24.12.2013)
Published in Journal of the American College of Cardiology (24.12.2013)
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Conference Proceeding
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
Miller, David T., Lee, Kristy, Gordon, Adam S., Amendola, Laura M., Adelman, Kathy, Bale, Sherri J., Chung, Wendy K., Gollob, Michael H., Harrison, Steven M., Herman, Gail E., Hershberger, Ray E., Klein, Teri E., McKelvey, Kent, Richards, C. Sue, Vlangos, Christopher N., Stewart, Douglas R., Watson, Michael S., Martin, Christa Lese
Published in Genetics in medicine (01.08.2021)
Published in Genetics in medicine (01.08.2021)
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The genetics of isolated congenital heart disease
Nees, Shannon N., Chung, Wendy K.
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.03.2020)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.03.2020)
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Pediatric Cardiomyopathies
Lee, Teresa M, Hsu, Daphne T, Kantor, Paul, Towbin, Jeffrey A, Ware, Stephanie M, Colan, Steven D, Chung, Wendy K, Jefferies, John L, Rossano, Joseph W, Castleberry, Chesney D, Addonizio, Linda J, Lal, Ashwin K, Lamour, Jacqueline M, Miller, Erin M, Thrush, Philip T, Czachor, Jason D, Razoky, Hiedy, Hill, Ashley, Lipshultz, Steven E
Published in Circulation research (15.09.2017)
Published in Circulation research (15.09.2017)
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Rare variant phasing and haplotypic expression from RNA sequencing with phASER
Castel, Stephane E., Mohammadi, Pejman, Chung, Wendy K., Shen, Yufeng, Lappalainen, Tuuli
Published in Nature communications (08.09.2016)
Published in Nature communications (08.09.2016)
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ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Miller, David T., Lee, Kristy, Abul-Husn, Noura S., Amendola, Laura M., Brothers, Kyle, Chung, Wendy K., Gollob, Michael H., Gordon, Adam S., Harrison, Steven M., Hershberger, Ray E., Klein, Teri E., Richards, C. Sue, Stewart, Douglas R., Martin, Christa Lese
Published in Genetics in medicine (01.08.2023)
Published in Genetics in medicine (01.08.2023)
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Observational study of spinal muscular atrophy type I and implications for clinical trials
Finkel, Richard S, McDermott, Michael P, Kaufmann, Petra, Darras, Basil T, Chung, Wendy K, Sproule, Douglas M, Kang, Peter B, Foley, A Reghan, Yang, Michelle L, Martens, William B, Oskoui, Maryam, Glanzman, Allan M, Flickinger, Jean, Montes, Jacqueline, Dunaway, Sally, O'Hagen, Jessica, Quigley, Janet, Riley, Susan, Benton, Maryjane, Ryan, Patricia A, Montgomery, Megan, Marra, Jonathan, Gooch, Clifton, De Vivo, Darryl C
Published in Neurology (26.08.2014)
Published in Neurology (26.08.2014)
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