المؤلفون: Mittendorf, Kathleen F, Kauffman, Tia L, Amendola, Laura M, Anderson, Katherine P, Biesecker, Barbara B, Dorschner, Michael O, Duenas, Devan M, Eubanks, Donna J, Feigelson, Heather Spencer, Gilmore, Marian J, Hunter, Jessica Ezzell, Joseph, Galen, Kraft, Stephanie A, Lee, Sandra Soo Jin, Leo, Michael C, Liles, Elizabeth G, Lindberg, Nangel M, Muessig, Kristin R, Okuyama, Sonia, Porter, Kathryn M, Riddle, Leslie S, Rolf, Bradley A, Rope, Alan F, Zepp, Jamilyn M, Jarvik, Gail P, Wilfond, Benjamin S, Goddard, Katrina AB, team, on behalf of the CHARM study

مصطلحات موضوعية: Prevention, Health Services, Genetic Testing, Human Genome, Clinical Research, Cancer, Genetics, 7.1 Individual care needs, Management of diseases and conditions, Good Health and Well Being, Genetic Counseling, Genomics, Healthcare Disparities, Humans, Neoplasms, Genetic counseling, Hereditary cancer, Family history, Underserved populations, CHARM study team, Medical and Health Sciences, General Clinical Medicine, Public Health

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3mv452fn

المؤلفون: Allen, Jake, Angelo, Frank, Arnold, Briana L., Bellcross, Cecelia, Bendelow, Tiffany, B, Barbara, Biesecker, Breslin, Kristin D., Booker, Kristina F., Caruncho, Mikaella, Davis, James V., Deutsch, Sonia, Devine, Beth, Dorschner, Michael O., Duenas, Devan, Eubanks, Donna J., Feigelson, Heather Spencer, Freed, Amanda S., Greaney, Clay, Gruß, Inga, Guerra, Claudia, Guo, Boya, Holup, Joan, Ingphakorn, Chalinya L., Jackson, Paige, Jarvik, Gail P., Jenkins, Charisma L., Karliner, Leah S., Kaufmann, Tia, Keast, Erin, Knerr, Sarah, Koomas, Alyssa H., Kraft, Stephanie A., Lee, Mi H., Lee, Robin, Soo-Jin Lee, Sandra, Lewis, Hannah S., Liles, Elizabeth G., Lindberg, Nangel M., Lynch, Frances, McMullen, Carmit K., Medina, Elizabeth, Mittendorf, Kathleen F., Muessig, Kristin R., Okuyama, Sonia, Peterson, C. Samuel, Paolucci, Angela R., Perez, Rosse Rodriguez, Porter, Kathryn M., Ransom, Chelese L., Reyes, Ana, Robinson, Sperry, Rolf, Bradley A., Rope, Alan F., Schield, Emily, Schneider, Jennifer L., Shipman, Kelly J., Shirts, Brian H., Shuster, Elizabeth, Syngal, Sapna, Torgrimson-Ojerio, Britta N., Ukaegbu, Chinedu, Vandermeer, Meredith L., Varga, Alexandra M., Veenstra, David L., Whitebirch, W. Chris, Lee White, Larissa, Hunter, Jessica Ezzell, Riddle, Leslie, Joseph, Galen, Amendola, Laura M., Gilmore, Marian J., Zepp, Jamilyn M., Bulkley, Joanna E., Anderson, Katherine P., Goddard, Katrina A.B., Wilfond, Benjamin S., Leo, Michael C.

المصدر: In Genetics in Medicine November 2023 25(11)

المؤلفون: Korvatska, Olena, Bucks, Stephanie A., Yoda, Rebecca A., Nolan, Amber, Dorschner, Michael O., Tsuang, Debby, Jayadev, Suman, Raskind, Wendy H., Bird, Thomas D.

المصدر: In Journal of the Neurological Sciences 15 September 2023 452

المؤلفون: Rosenthal, Elisabeth A, Shirts, Brian H, Amendola, Laura M, Horike-Pyne, Martha, Robertson, Peggy D, Hisama, Fuki M, Bennett, Robin L, Dorschner, Michael O, Nickerson, Deborah A, Stanaway, Ian B, Nassir, Rami, Vickers, Kathy T, Li, Christopher, Grady, William M, Peters, Ulrike, Jarvik, Gail P, NHLBI GO Exome Sequencing Project

المصدر: Human Genetics. 137(10)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Genetics, Clinical Research, Digestive Diseases, Colo-Rectal Cancer, Cancer, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Adult, Aged, Aged, 80 and over, BRCA2 Protein, Colorectal Neoplasms, Deoxyribonuclease (Pyrimidine Dimer), Fanconi Anemia Complementation Group Proteins, Female, Genetic Loci, Genetic Variation, Humans, Male, Middle Aged, RNA Helicases, Risk Factors, NHLBI GO Exome Sequencing Project, Complementary and Alternative Medicine, Paediatrics and Reproductive Medicine, Genetics & Heredity, Reproductive medicine

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/23p7p5p8

المؤلفون: O'Daniel, Julianne M, McLaughlin, Heather M, Amendola, Laura M, Bale, Sherri J, Berg, Jonathan S, Bick, David, Bowling, Kevin M, Chao, Elizabeth C, Chung, Wendy K, Conlin, Laura K, Cooper, Gregory M, Das, Soma, Deignan, Joshua L, Dorschner, Michael O, Evans, James P, Ghazani, Arezou A, Goddard, Katrina A, Gornick, Michele, Farwell Hagman, Kelly D, Hambuch, Tina, Hegde, Madhuri, Hindorff, Lucia A, Holm, Ingrid A, Jarvik, Gail P, Knight Johnson, Amy, Mighion, Lindsey, Morra, Massimo, Plon, Sharon E, Punj, Sumit, Richards, C Sue, Santani, Avni, Shirts, Brian H, Spinner, Nancy B, Tang, Sha, Weck, Karen E, Wolf, Susan M, Yang, Yaping, Rehm, Heidi L

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 19(5)

مصطلحات موضوعية: Disclosure, Genetic Testing: methods, standards, Humans, Incidental Findings, Information Dissemination, Laboratories: ethics, standards, Practice Guidelines as Topic, Research Report, Sample Size, Sequence Analysis, DNA: methods, standards, Surveys and Questionnaires

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/36w1z6tw

المؤلفون: Mata, Ignacio F, Davis, Marie Y, Lopez, Alexis N, Dorschner, Michael O, Martinez, Erica, Yearout, Dora, Cholerton, Brenna A, Hu, Shu‐Ching, Edwards, Karen L, Bird, Thomas D, Zabetian, Cyrus P

المصدر: American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(7)

مصطلحات موضوعية: Biological Sciences, Genetics, Parkinson's Disease, Brain Disorders, Neurosciences, Neurodegenerative, Aging, 2.1 Biological and endogenous factors, Aetiology, Neurological, Aged, DNA Mutational Analysis, Female, Genetic Predisposition to Disease, Haplotypes, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Middle Aged, Mutation, Missense, Parkinson Disease, Pedigree, Risk Factors, movement disorders, genetics, neuropsychological, Clinical Sciences, Clinical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9xh6d235

المؤلفون: Dorschner, Michael O.^Aff3

المساهمون: Netto, George Jabboure, editor^Aff1, Kaul, Karen L., editor^Aff2

المصدر: Genomic Applications in Pathology. :191-202

المؤلفون: Blau, C Anthony, Ramirez, Arturo B, Blau, Sibel, Pritchard, Colin C, Dorschner, Michael O, Schmechel, Stephen C, Martins, Timothy J, Mahen, Elisabeth M, Burton, Kimberly A, Komashko, Vitalina M, Radenbaugh, Amie J, Dougherty, Katy, Thomas, Anju, Miller, Christopher P, Annis, James, Fromm, Jonathan R, Song, Chaozhong, Chang, Elizabeth, Howard, Kellie, Austin, Sharon, Schmidt, Rodney A, Linenberger, Michael L, Becker, Pamela S, Senecal, Francis M, Mecham, Brigham H, Lee, Su-In, Madan, Anup, Ronen, Roy, Dutkowski, Janusz, Heimfeld, Shelly, Wood, Brent L, Stilwell, Jackie L, Kaldjian, Eric P, Haussler, David, Zhu, Jingchun

المصدر: Journal of the National Comprehensive Cancer Network. 14(1)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Biotechnology, Cancer, Clinical Research, Clinical Trials and Supportive Activities, Breast Cancer, Good Health and Well Being, Antineoplastic Combined Chemotherapy Protocols, Bone Neoplasms, Community Networks, Drug Resistance, Neoplasm, Drug Screening Assays, Antitumor, Expert Testimony, Female, Follow-Up Studies, Humans, Leukapheresis, Longitudinal Studies, Middle Aged, Neoplasm Metastasis, Neoplastic Cells, Circulating, Research Personnel, Triple Negative Breast Neoplasms, Oncology & Carcinogenesis, Oncology and carcinogenesis, Health services and systems

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3236q55n

المؤلفون: Mata, Ignacio F, Jang, Yongwoo, Kim, Chun-Hyung, Hanna, David S, Dorschner, Michael O, Samii, Ali, Agarwal, Pinky, Roberts, John W, Klepitskaya, Olga, Shprecher, David R, Chung, Kathryn A, Factor, Stewart A, Espay, Alberto J, Revilla, Fredy J, Higgins, Donald S, Litvan, Irene, Leverenz, James B, Yearout, Dora, Inca-Martinez, Miguel, Martinez, Erica, Thompson, Tiffany R, Cholerton, Brenna A, Hu, Shu-Ching, Edwards, Karen L, Kim, Kwang-Soo, Zabetian, Cyrus P

المصدر: Molecular Neurodegeneration. 10(1)

مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Neurosciences, Parkinson's Disease, Clinical Research, Human Genome, Aging, Prevention, Neurodegenerative, Brain Disorders, 2.1 Biological and endogenous factors, Aetiology, Neurological, Adult, Age of Onset, Animals, Exome, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Middle Aged, Mutation, Parkinson Disease, Phenotype, Rats, rab GTP-Binding Proteins, Clinical Sciences, Neurology & Neurosurgery, Biochemistry and cell biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6446j25p

المؤلفون: Amendola, Laura M, Dorschner, Michael O, Robertson, Peggy D, Salama, Joseph S, Hart, Ragan, Shirts, Brian H, Murray, Mitzi L, Tokita, Mari J, Gallego, Carlos J, Kim, Daniel Seung, Bennett, James T, Crosslin, David R, Ranchalis, Jane, Jones, Kelly L, Rosenthal, Elisabeth A, Jarvik, Ella R, Itsara, Andy, Turner, Emily H, Herman, Daniel S, Schleit, Jennifer, Burt, Amber, Jamal, Seema M, Abrudan, Jenica L, Johnson, Andrew D, Conlin, Laura K, Dulik, Matthew C, Santani, Avni, Metterville, Danielle R, Kelly, Melissa, Foreman, Ann Katherine M, Lee, Kristy, Taylor, Kent D, Guo, Xiuqing, Crooks, Kristy, Kiedrowski, Lesli A, Raffel, Leslie J, Gordon, Ora, Machini, Kalotina, Desnick, Robert J, Biesecker, Leslie G, Lubitz, Steven A, Mulchandani, Surabhi, Cooper, Greg M, Joffe, Steven, Richards, C Sue, Yang, Yaoping, Rotter, Jerome I, Rich, Stephen S, O’Donnell, Christopher J, Berg, Jonathan S, Spinner, Nancy B, Evans, James P, Fullerton, Stephanie M, Leppig, Kathleen A, Bennett, Robin L, Bird, Thomas, Sybert, Virginia P, Grady, William M, Tabor, Holly K, Kim, Jerry H, Bamshad, Michael J, Wilfond, Benjamin, Motulsky, Arno G, Scott, C Ronald, Pritchard, Colin C, Walsh, Tom D, Burke, Wylie, Raskind, Wendy H, Byers, Peter, Hisama, Fuki M, Rehm, Heidi, Nickerson, Debbie A, Jarvik, Gail P

المصدر: Genome Research. 25(3)

مصطلحات موضوعية: Biological Sciences, Genetics, Biotechnology, Human Genome, Clinical Research, Good Health and Well Being, Adult, Black People, Exome, Female, Gene Frequency, Genes, Dominant, Genetic Association Studies, Genetic Testing, Genome, Human, Genomics, High-Throughput Nucleotide Sequencing, Humans, Incidental Findings, Male, Phenotype, Polymorphism, Single Nucleotide, White People, Medical and Health Sciences, Bioinformatics

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/19w813v8