检索结果 - Andersen, Erica
- Showing 1 - 13 results of 13
-
1
-
2
-
3
-
4
-
5
-
6
-
7
Alternative ESC and ESC-Like Subunits of a Polycomb Group Histone Methyltransferase Complex Are Differentially Deployed during Drosophila Development 由 Wang, Liangjun, Jahren, Neal, Vargas, Marcus L., Andersen, Erica F., Benes, Judith, Zhang, Junyu, Miller, Ellen L., Jones, Richard S., Simon, Jeffrey A.
出版 2006Text -
8
Utilizing ClinGen Gene-Disease Validity and Dosage Sensitivity Curations to Inform Variant Classification 由 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
出版 2022Text -
9
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... 由 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
出版 2019Text -
10
GENOMIC ANALYSES IDENTIFY RECURRENT ALTERATIONS IN IMMUNE EVASION GENES IN DIFFUSE LARGE B CELL LYMPHOMA, LEG TYPE 由 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
出版 2018Text -
11
Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features 由 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.
出版 2020Text -
12
Genomic landscape of cutaneous follicular lymphomas reveals 2 subgroups with clinically predictive molecular features 由 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
出版 2021Text -
13
Copy Number Variant Discrepancy Resolution Using the ClinGen Dosage Sensitivity Map Results in Updated Clinical Interpretations in ClinVar 由 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.
出版 2018Text