Výsledky vyhledávání - Andersen, Erica
- Zobrazuji výsledky 1 - 13 z 13
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Elements of the Polycomb Repressor SU(Z)12 Needed for Histone H3-K27 Methylation, the Interface with E(Z), and In Vivo Function Autor Rai, Aswathy N., Vargas, Marcus L., Wang, Liangjun, Andersen, Erica F., Miller, Ellen L., Simon, Jeffrey A.
Vydáno 2013Text -
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Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf–Hirschhorn Syndrome Autor Andersen, Erica F, Carey, John C, Earl, Dawn L, Corzo, Deyanira, Suttie, Michael, Hammond, Peter, South, Sarah T
Vydáno 2014Text -
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Alternative ESC and ESC-Like Subunits of a Polycomb Group Histone Methyltransferase Complex Are Differentially Deployed during Drosophila Development Autor Wang, Liangjun, Jahren, Neal, Vargas, Marcus L., Andersen, Erica F., Benes, Judith, Zhang, Junyu, Miller, Ellen L., Jones, Richard S., Simon, Jeffrey A.
Vydáno 2006Text -
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Utilizing ClinGen Gene-Disease Validity and Dosage Sensitivity Curations to Inform Variant Classification Autor Thaxton, Courtney, Good, Molly E., DiStefano, Marina T., Luo, Xi, Andersen, Erica F., Thorland, Erik, Berg, Jonathan, Martin, Christa Lese, Rehm, Heidi L., Riggs, Erin Rooney
Vydáno 2022Text -
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Technical standards for the interpretation and reporting of constitutional copy number variants: a joint consensus recommendation of the American College of Medical Genetics and Ge... Autor Riggs, Erin Rooney, Andersen, Erica F., Cherry, Athena M., Kantarci, Sibel, Kearney, Hutton, Patel, Ankita, Raca, Gordana, Ritter, Deborah I., South, Sarah T., Thorland, Erik C., Pineda-Alvarez, Daniel, Aradhya, Swaroop, Martin, Christa Lese
Vydáno 2019Text -
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GENOMIC ANALYSES IDENTIFY RECURRENT ALTERATIONS IN IMMUNE EVASION GENES IN DIFFUSE LARGE B CELL LYMPHOMA, LEG TYPE Autor Zhou, Xiaolong Alan, Louissaint, Abner, Wenzel, Alexander, Yang, Jingyi, Martinez-Escala, Maria Estela, Moy, Andrea P., Morgan, Elizabeth A., Paxton, Christian N., Hong, Bo, Andersen, Erica F., Guitart, Joan, Behdad, Amir, Cerroni, Lorenzo, Weinstock, David M., Choi, Jaehyuk
Vydáno 2018Text -
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Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features Autor Ballout, Rami A., Dickerson, Cheryl, Wick, Myra J., Al-Sweel, Najla, Openshaw, Amanda S., Srivastava, Siddharth, Swanson, Lindsay, Bramswig, Nuria C., Kuechler, Alma, Hong, Bo, Fleming, Leah R., Curry, KT, Robertson, Stephen P., Andersen, Erica F., El-Hattab, Ayman W.
Vydáno 2020Text -
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Genomic landscape of cutaneous follicular lymphomas reveals 2 subgroups with clinically predictive molecular features Autor Zhou, Xiaolong Alan, Yang, Jingyi, Ringbloom, Kimberly G., Martinez-Escala, Maria Estela, Stevenson, Kristen E., Wenzel, Alexander T., Fantini, Damiano, Martin, Haley K., Moy, Andrea P., Morgan, Elizabeth A., Harkins, Shannon, Paxton, Christian N., Hong, Bo, Andersen, Erica F., Guitart, Joan, Weinstock, David M., Cerroni, Lorenzo, Choi, Jaehyuk, Louissaint, Abner
Vydáno 2021Text -
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Copy Number Variant Discrepancy Resolution Using the ClinGen Dosage Sensitivity Map Results in Updated Clinical Interpretations in ClinVar Autor Riggs, Erin R., Nelson, Tristan, Merz, Andrew, Ackley, Todd, Bunke, Brian, Collins, Christin D., Collinson, Morag N., Fan, Yao-Shan, Goodenberger, McKinsey L., Golden, Denae M., Haglund-Hazy, Linda, Krgovic, Danijela, Lamb, Allen N., Lewis, Zoe, Li, Guang, Liu, Yajuan, Meck, Jeanne, Neufeld-Kaiser, Whitney, Runke, Cassandra K., Sanmann, Jennifer N., Stavropoulos, Dimitri J., Strong, Emma, Su, Meng, Tayeh, Marwan K., Vokac, Nadja Kokalj, Thorland, Erik C., Andersen, Erica, Martin, Christa L.
Vydáno 2018Text