Genetics and genomics of pulmonary arterial hypertension von Morrell, Nicholas W, Aldred, Micheala A, Chung, Wendy K, Elliott, C Gregory, Nichols, William C, Soubrier, Florent, Trembath, Richard C, Loyd, James E

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Universal newborn screening using genome sequencing: early experience from the GUARDIAN study von Ziegler, Alban, Chung, Wendy K

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Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association von 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.

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Genetic Basis of Human Congenital Heart Disease von Nees, Shannon N., Chung, Wendy K.

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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) von 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

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MVP predicts the pathogenicity of missense variants by deep learning von Qi, Hongjian, Zhang, Haicang, Zhao, Yige, Chen, Chen, Long, John J., Chung, Wendy K., Guan, Yongtao, Shen, Yufeng

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The role of genetics in pulmonary arterial hypertension von Ma, Lijiang, Chung, Wendy K

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Clinical application of whole-exome sequencing across clinical indications von 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

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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 Genet... von 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.

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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) von 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

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Genetics and Genomics of Pulmonary Arterial Hypertension von 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

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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) von 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.

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Recent insights into peroxisome biogenesis and associated diseases von Fujiki, Yukio, Abe, Yuichi, Imoto, Yuuta, Tanaka, Akemi J., Okumoto, Kanji, Honsho, Masanori, Tamura, Shigehiko, Miyata, Non, Yamashita, Toshihide, Chung, Wendy, Kuroiwa, Tsuneyoshi

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De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders von Qi, Hongjian, Yu, Lan, Zhou, Xueya, Wynn, Julia, Zhao, Haoquan, Guo, Yicheng, Zhu, Na, Kitaygorodsky, Alexander, Hernan, Rebecca, Aspelund, Gudrun, Lim, Foong-Yen, Crombleholme, Timothy, Cusick, Robert, Azarow, Kenneth, Danko, Melissa E, Chung, Dai, Warner, Brad W, Mychaliska, George B, Potoka, Douglas, Wagner, Amy J, ElFiky, Mahmoud, Wilson, Jay M, Nickerson, Debbie, Bamshad, Michael, High, Frances A, Longoni, Mauro, Donahoe, Patricia K, Chung, Wendy K, Shen, Yufeng

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Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials von Clément, Karine, van den Akker, Erica, Argente, Jesús, Bahm, Allison, Chung, Wendy K, Connors, Hillori, De Waele, Kathleen, Farooqi, I Sadaf, Gonneau-Lejeune, Julie, Gordon, Gregory, Kohlsdorf, Katja, Poitou, Christine, Puder, Lia, Swain, James, Stewart, Murray, Yuan, Guojun, Wabitsch, Martin, Kühnen, Peter, Pigeon-Kherchiche, Patricia, Flaus-Furmaniuk, Anna, Bald, Martin, Denzer, Christian, von Schnurbein, Julia, Abawi, Ozair, Blume-Peytavi, Ulrike, Krabusch, Philipp, Mai, Knut, Schnabel, Dirk, Wiegand, Susanna, Flück, Christa E, Schulz, Esther, Voss, Egbert, Bratina, Natasa, Weiss, Katja, Martos-Moreno, Gabriel Á, Danset, Alban, Gougis, Paul, Dubern, Béatrice, Clément, Karine, van den Akker, Erica L.T., Argente, Jesús, Bahm, Allison L, Chung, Wendy K, Connors, Hillori S, De Waele, Kathleen, Farooqi, Ismaa Sadaf, Gonneau-Lejeune, Julie, Gordon, Gregory A, Poitou, Christine, Puder, Lia, Swain, James M, Stewart, Murray W, Yuan, Goujun, Wabitsch, Martin, Kühnen, Peter

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Recent advances in understanding neuro von Ziegler, Alban, Chung, Wendy K

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Genetics and Other Omics in Pediatric Pulmonary Arterial Hypertension von Welch, Carrie L., Chung, Wendy K.

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The genetic basis of pulmonary arterial hypertension von Ma, Lijiang, Chung, Wendy K.

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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 Genomic... von 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

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The influence of genetics in congenital diaphragmatic hernia von Yu, Lan, Hernan, Rebecca R., Wynn, Julia, Chung, Wendy K.

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