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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Malformation syndromes caused by disorders of cholesterol synthesis von Porter, Forbes D., Herman, Gail E.

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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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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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Endogenous Sterol Metabolites Regulate Growth of EGFR/KRAS-Dependent Tumors via LXR von Gabitova, Linara, Restifo, Diana, Gorin, Andrey, Manocha, Kunal, Handorf, Elizabeth, Yang, Dong-Hua, Cai, Kathy Q., Klein-Szanto, Andres J., Cunningham, David, Kratz, Lisa E., Herman, Gail E., Golemis, Erica A., Astsaturov, Igor

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Analysis of hedgehog signaling in cerebellar granule cell precursors in a conditional Nsdhl allele demonstrates an essential role for cholesterol in postnatal CNS development von Cunningham, David, DeBarber, Andrea E, Bir, Natalie, Binkley, Laura, Merkens, Louise S, Steiner, Robert D, Herman, Gail E

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Reporting genomic secondary findings: ACMG members weigh in von Scheuner, Maren T., Peredo, Jane, Benkendorf, Judith, Bowdish, Bruce, Feldman, Gerald, Fleisher, Lynn, Mulvihill, John J., Watson, Michael, Herman, Gail E., Evans, James

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Correction to: 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 Gen... 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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Targeting C4-demethylating genes in the cholesterol pathway sensitizes cancer cells to EGF receptor inhibitors via increased EGF receptor degradation von Sukhanova, Anna, Gorin, Andrey, Serebriiskii, Ilya G, Gabitova, Linara, Zheng, Hui, Restifo, Diana, Egleston, Brian L, Cunningham, David, Bagnyukova, Tetyana, Liu, Hanqing, Nikonova, Anna, Adams, Gregory P, Zhou, Yan, Yang, Dong-Hua, Mehra, Ranee, Burtness, Barbara, Cai, Kathy Q, Klein-Szanto, Andres, Kratz, Lisa E, Kelley, Richard I, Weiner, Louis M, Herman, Gail E, Golemis, Erica A, Astsaturov, Igor

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Analysis of two candidate genes for Basan syndrome von Marks, Katherine C., Banks III, Wesley R., Cunningham, David, Witman, Patricia M., Herman, Gail E.

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Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay von Muller, Eric A., Aradhya, Swaroop, Atkin, Joan F., Carmany, Erin P., Elliott, Alison M., Chudley, Albert E., Clark, Robin D., Everman, David B., Garner, Shannon, Hall, Bryan D., Herman, Gail E., Kivuva, Emma, Ramanathan, Subhadra, Stevenson, David A., Stockton, David W., Hudgins, Louanne

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Contactin 4 as an autism susceptibility locus von Cottrell, Catherine E., Bir, Natalie, Varga, Elizabeth, Alvarez, Carlos E., Bouyain, Samuel, Zernzach, Randall, Thrush, Devon L., Evans, Johnna, Trimarchi, Michael, Butter, Eric M., Cunningham, David, Gastier-Foster, Julie M., McBride, Kim L., Herman, Gail E.

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The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly von Varga, Elizabeth A., Pastore, Matthew, Prior, Thomas, Herman, Gail E., McBride, Kim L.

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Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research von Manolio, Teri A., Fowler, Douglas M., Starita, Lea M., Haendel, Melissa A., MacArthur, Daniel G., Biesecker, Leslie G., Worthey, Elizabeth, Chisholm, Rex L., Green, Eric D., Jacob, Howard J., McLeod, Howard L., Roden, Dan, Rodriguez, Laura Lyman, Williams, Marc S., Cooper, Gregory M., Cox, Nancy J., Herman, Gail E., Kingsmore, Stephen, Lo, Cecilia, Lutz, Cathleen, MacRae, Calum A., Nussbaum, Robert L., Ordovas, Jose M., Ramos, Erin M., Robinson, Peter N., Rubinstein, Wendy S., Seidman, Christine, Stranger, Barbara E., Wang, Haoyi, Westerfield, Monte, Bult, Carol

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Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ3 Variant von Arredondo, Kristen, Myers, Cortlandt, Hansen-Kiss, Emily, Mathew, Mariam T., Jayaraman, Vijayakumar, Siemon, Amy, Bartholomew, Dennis, Herman, Gail E., Mori, Mari

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Hematopoietic cell transplantation for a child with OSTM1 osteopetrosis von Overholt, Kathleen M., Rose, Melissa J., Joshi, Sarita, Herman, Gail E., Bajwa, Rajinder, Abu-Arja, Rolla, Rangarajan, Hemalatha G., Horwitz, Edwin M.

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Disorders of cholesterol biosynthesis: prototypic metabolic malformation syndromes von Herman, Gail E

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Human CRMP4 mutation and disrupted Crmp4 expression in mice are associated with ASD characteristics and sexual dimorphism von Tsutiya, Atsuhiro, Nakano, Yui, Hansen-Kiss, Emily, Kelly, Benjamin, Nishihara, Masugi, Goshima, Yoshio, Corsmeier, Don, White, Peter, Herman, Gail E., Ohtani-Kaneko, Ritsuko

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Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly von McBride, Kim L., Varga, Elizabeth A., Pastore, Matthew T., Prior, Thomas W., Manickam, Kandamurugu, Atkin, Joan F., Herman, Gail E.

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Chinese hamster ovary cell-derived recombinant human acid α-glucosidase in infantile-onset Pompe disease von Kishnani, Priya Sunil, Nicolino, Marc, Voit, Thomas, Rogers, R. Curtis, Tsai, Anne Chun-Hui, Waterson, John, Herman, Gail E., Amalfitano, Andreas, Thurberg, Beth L., Richards, Susan, Davison, Mark, Corzo, Deyanira, Chen, Y.T.

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