Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Myra J Wick"'
Autor:
Grayson B. Ashby, Kirsten A. Riggan, Lily Huang, Vanessa E. Torbenson, Margaret E. Long, Myra J. Wick, Megan A. Allyse, Enid Y. Rivera-Chiauzzi
Publikováno v:
BMC Pregnancy and Childbirth, Vol 22, Iss 1, Pp 1-11 (2022)
Abstract Background The COVID-19 pandemic has posed profound challenges for pregnant patients and their families. Studies conducted early in the pandemic found that pregnant individuals reported increased mental health concerns in response to pandemi
Externí odkaz:
https://doaj.org/article/fe7cad4c214c46b3bb3cf4b856618859
Autor:
Linda J. Tostrud, Vesna D. Garovic, Layan Alrahmani, Ann M. Moyer, Kavita Narang, Maria Alice V. Willrich, Myra J. Wick, Maria L. Gonzalez Suarez, Wendy M. White, Margot A. Cousin
Publikováno v:
Kidney360
BACKGROUND: Preeclampsia and hemolysis, elevated liver enzymes, and low platelets (HELLP) syndrome share many clinical and biologic features with thrombotic microangiopathy syndromes caused by complement abnormalities. Our hypothesis was that similar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ad9e5735844b93b41ffa38933586e29
https://doi.org/10.34067/kid.0000992021
https://doi.org/10.34067/kid.0000992021
Autor:
Judith Balmaña, Nicoleta C. Voian, Tuya Pal, Joanne Ngeow, Douglas R. Stewart, Myra J. Wick, Paul A. James, Marc Tischkowitz, Rita K. Schmutzler, William D. Foulkes
Publikováno v:
Genetics in Medicine. 23:1416-1423
Purpose PALB2 germline pathogenic variants are associated with increased breast cancer risk and smaller increased risk of pancreatic and likely ovarian cancer. Resources for health-care professionals managing PALB2 heterozygotes are currently limited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4b282d8dc93a730b7b42135483845d5
https://doi.org/10.1038/s41436-021-01151-8
https://doi.org/10.1038/s41436-021-01151-8
Autor:
Bright P. Thilagar, Aditya K. Ghosh, Jerome Nguyen, Regan N. Theiler, Myra J. Wick, Ryan T. Hurt, Raymund R. Razonable, Ravindra Ganesh
Publikováno v:
Obstetrics & Gynecology. 139:616-618
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::605bd21a26dfeebaa8488f5fdc6694a0
https://doi.org/10.1097/aog.0000000000004700
https://doi.org/10.1097/aog.0000000000004700
Autor:
Niloy Jewel Samadder, Brenda Ernst, Scott H. Okuno, Myra J. Wick, Robert L. Nussbaum, Keith Stewart, Megan M. Hager, Pls Uson Junior, Cindy Azevedo, Douglas L. Riegert-Johnson, Margaret Klint, Michael A. Golafshar, Edward D. Esplin, Donald W. Northfelt, Deborah J. Rhodes, Katie L. Kunze, Sarah Mantia, Natalie Ertz-Archambault
Publikováno v:
Cancer Research. 81:PD10-05
Background: Hereditary factors play a key role in the risk of developing breast cancers. Identification of a germline predisposition can have important implications for treatment decisions, risk-reducing interventions, cancer screening, and testing f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88204478e38afcf78c74948755da7134
https://doi.org/10.1158/1538-7445.sabcs20-pd10-05
https://doi.org/10.1158/1538-7445.sabcs20-pd10-05
Autor:
Jennifer K. Litton, Kenneth Offit, Christine Laronga, Matthew B. Yurgelun, Leigha Senter-Jamieson, Kristen M. Shannon, Ahmed Elkhanany, Beth Y. Karlan, Seema A. Khan, Susan M. Domchek, Kari B. Wisinski, Patricia I. Dickson, Gwen Reiser, Holly J. Pederson, Catherine Klein, Barbara S. Norquist, Mary B. Daly, Allison W. Kurian, Wendy Kohlmann, Carolyn S. Menendez, Jeffrey N. Weitzel, Mary A. Dwyer, Mollie L. Hutton, Susan Darlow, Kala Visvanathan, Sofia D. Merajver, Rebecca Shatsky, Myra J. Wick, Michael Goggins, Saundra S. Buys, Michael Berry, Susan Hatters Friedman, Julie S. Mak, Tuya Pal
Publikováno v:
Journal of the National Comprehensive Cancer Network. 19:77-102
The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic focus primarily on assessment of pathogenic or likely pathogenic variants associated with increased risk of breast, ovarian, and pancreatic cancer and reco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9b57ad3ed257825a4301e48dcd971c4
https://doi.org/10.6004/jnccn.2021.0001
https://doi.org/10.6004/jnccn.2021.0001
Autor:
Yang Cao, Nicole L. Hoppman, Sarah E. Kerr, Christopher A. Sattler, Kristi S. Borowski, Myra J. Wick, W. Edward Highsmith, Umut Aypar
Publikováno v:
Case Reports in Genetics, Vol 2016 (2016)
Background. Noninvasive prenatal screening (NIPS) is revolutionizing prenatal screening as a result of its increased sensitivity, specificity. NIPS analyzes cell-free fetal DNA (cffDNA) circulating in maternal plasma to detect fetal chromosome abnorm
Externí odkaz:
https://doaj.org/article/4a14796c75b14734b40e7acbe70c9981
Autor:
Eric W. Klee, Eva Morava, Rodrigo Tzovenos Starosta, Laura Rust, Wasantha Ranatunga, Alejandro Ferrer, Dani Ungar, Myra J. Wick, Tamas Kozicz
Publikováno v:
Molecular Genetics and Metabolism. 131:424-429
Introduction Congenital disorders of glycosylation (CDG) are inborn errors of glycan metabolism with high clinical variability. Only a few antenatal cases have been described with CDG. Due to a lack of reliable biomarker, prenatal CDG diagnostics rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29c44bcfc9a05e8aa3c409638cb96267
https://doi.org/10.1016/j.ymgme.2020.11.003
https://doi.org/10.1016/j.ymgme.2020.11.003
Autor:
Mollie L. Hutton, Mary A. Dwyer, Catherine Klein, Robert Pilarski, Kala Visvanathan, Michael Goggins, Susan Darlow, Myra J. Wick, Carolyn S. Menendez, Jennifer K. Litton, Kenneth Offit, Gwen Reiser, Seema A. Khan, Holly J. Pederson, Matthew B. Yurgelun, Patricia I. Dickson, Mary B. Daly, Allison W. Kurian, Christine Laronga, Sofia D. Merajver, Kari B. Wisinski, Barbara S. Norquist, Michael Berry, Saundra S. Buys, Susan Hatters Friedman, Wendy Kohlmann, Jeffrey N. Weitzel, Julie S. Mak, Ahmed Elkhanany, Judy Garber, Kristen M. Shannon, Susan M. Domchek, Tuya Pal
Publikováno v:
Journal of the National Comprehensive Cancer Network. 18:380-391
The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic provide recommendations for genetic testing and counseling for hereditary cancer syndromes, and risk management recommendations for patients who are diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b39e974208603592707867505730eb8e
https://doi.org/10.6004/jnccn.2020.0017
https://doi.org/10.6004/jnccn.2020.0017
Autor:
Alma Kuechler, Amanda Openshaw, Stephen P. Robertson, Siddharth Srivastava, Bo Hong, Leah R Fleming, Cheryl Dickerson, Lindsay C. Swanson, Kathryn Curry, Rami A. Ballout, Najla Al-Sweel, Myra J. Wick, Nuria C. Bramswig, Ayman W. El-Hattab, Erica F. Andersen
Publikováno v:
Hum Mutat
Int22h1/Int22h2-mediated Xq28 duplication syndrome is a relatively new X-linked intellectual disability syndrome, arising from duplications of the subregion flanked by intron 22 homologous regions 1 and 2 on the q arm of chromosome X. Its primary man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e0be034c3119b8ef59945e2af31da28
https://doi.org/10.1002/humu.24009
https://doi.org/10.1002/humu.24009