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M

Myra I. Roche

University of North Carolina
H指数:25
被引数:2,285

个人简介

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教育背景

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工作经历

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荣誉奖项

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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project

新生儿筛查的基因组测序: NC NEXUS项目的结果

AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2020-10-0178
OAAI
Roman, Tamara S.; Crowley, Stephanie B.; Roche, Myra, I; Foreman, Ann Katherine M.; O'Daniel, Julianne M.; Seifert, Bryce A.; Lee, Kristy; Brandt, Alicia; Gustafson, Chelsea; DeCristo, Daniela M.; Strande, Natasha T.; Ramkissoon, Lori; Milko, Laura, V; Owen, Phillips; Roy, Sayanty; Xiong, Mai; Paquin, Ryan S.; Butterfield, Rita M.; Lewis, Megan A.; Souris, Katherine J.; Bailey, Donald B., Jr.; Rini, Christine; Booker, Jessica K.; Powell, Bradford C.; Weck, Karen E.; Powell, Cynthia M.; Berg, Jonathan S.
An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening
JOURNAL OF PEDIATRICS
IF3.5
2019-06-0158
OAAI
Milko, Laura, V; O'Daniel, Julianne M.; DeCristo, Daniela M.; Crowley, Stephanie B.; Foreman, Ann Katherine M.; Wallace, Kathleen E.; Mollison, Lonna F.; Strande, Natasha T.; Girnary, Zahra S.; Boshe, Lacey J.; Aylsworth, Arthur S.; Gucsavas-Calikoglu, Muge; Frazier, Dianne M.; Vora, Neeta L.; Roche, Myra, I; Powell, Bradford C.; Powell, Cynthia M.; Berg, Jonathan S.
Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background

开发一种概念性的，可重复的，基于规则的方法，以同意和结果披露具有最低遗传学背景的临床医生进行基因检测

GENETICS IN MEDICINE
IF6.2
2019-03-0141
OAAI
Ormond, Kelly E.; Hallquist, Miranda L. G.; Buchanan, Adam H.; Dondanville, Danielle; Cho, Mildred K.; Smith, Maureen; Roche, Myra; Brothers, Kyle B.; Coughlin, Curtis R., II; Hercher, Laura; Hudgins, Louanne; Jamal, Seema; Levy, Howard P.; Raskin, Misha; Stosic, Melissa; Uhlmann, Wendy; Wain, Karen E.; Currey, Erin; Faucett, W. Andrew
Newborn Sequencing in Genomic Medicine and Public Health

基因组医学和公共卫生中的新生儿测序

PEDIATRICS
IF6.4
2017-02-01183
OAAI
Berg, Jonathan S.; Agrawal, Pankaj B.; Bailey, Donald B., Jr.; Beggs, Alan H.; Brenner, Steven E.; Brower, Amy M.; Cakici, Julie A.; Ceyhan-Birsoy, Ozge; Chan, Kee; Chen, Flavia; Currier, Robert J.; Dukhovny, Dmitry; Green, Robert C.; Harris-Wai, Julie; Holm, Ingrid A.; Iglesias, Brenda; Joseph, Galen; Kingsmore, Stephen F.; Koenig, Barbara A.; Kwok, Pui-Yan; Lantos, John; Leeder, Steven J.; Lewis, Megan A.; McGuire, Amy L.; Milko, Laura V.; Mooney, Sean D.; Parad, Richard B.; Pereira, Stacey; Petrikin, Joshua; Powell, Bradford C.; Powell, Cynthia M.; Puck, Jennifer M.; Rehm, Heidi L.; Risch, Neil; Roche, Myra; Shieh, Joseph T.; Veeraraghavan, Narayanan; Watson, Michael S.; Willig, Laurel; Yu, Timothy W.; Urv, Tiina; Wise, Anastasia L.
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

用于评估来自基因组规模测序的偶然或次要发现的临床可操作性的半定量度量

GENETICS IN MEDICINE
IF6.2
2016-05-0171
OAAI
Berg, Jonathan S.; Foreman, Ann Katherine M.; O'Daniel, Julianne M.; Booker, Jessica K.; Boshe, Lacey; Carey, Timothy; Crooks, Kristy R.; Jensen, Brian C.; Juengst, Eric T.; Lee, Kristy; Nelson, Daniel K.; Powell, Bradford C.; Powell, Cynthia M.; Roche, Myra I.; Skrzynia, Cecile; Strande, Natasha T.; Weck, Karen E.; Wilhelmsen, Kirk C.; Evans, James P.

研究方向

暂未获取到该数据
J
Jonathan S. Berg
H 指数:61论文数:335被引数:2.1万
C
Cynthia M. Powell
H 指数:38论文数:158被引数:5,046
C
Christine Rini
H 指数:44论文数:257被引数:8,536
D
Donald B. Bailey
H 指数:73论文数:385被引数:1.6万
J
Julianne O’Daniel
H 指数:31论文数:189被引数:5,761
A
Ann Katherine M. Foreman
H 指数:16论文数:71被引数:1,619
G
Gail E. Henderson
H 指数:41论文数:250被引数:6,077
J
James P. Evans
H 指数:54论文数:212被引数:1.1万
B
Bradford C. Powell
H 指数:24论文数:96被引数:2,858
M
Megan A. Lewis
H 指数:46论文数:315被引数:8,603