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498 results for Chung,+Wendy

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ebooks
The impact of cultural differences on an Australian firm doing business in China [electronic resource] / Mona Chung & Wendy Smith.
Author / Creator:Chung, Mona.
Publisher:[Clayton, Vic.] : Monash University Dept. of Management, 2006.
Date:2006.
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Managing academic support for international students [electronic resource] : the appropriateness of a learning support unit in an Australian tertiary institution / Mona Chung, Martin kelliher & Wendy...
Author / Creator:Chung, Mona.
Publisher:[Clayton, Vic.] : Monash University Dept. of Management, 2006.
Date:2006.
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Books
Henry James in context / edited by David McWhirter.
Publisher:Cambridge ; New York : Cambridge University Press, c2010.
Call Numbers:N813.4/65
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Kibble Awards for Literature 2015 : entries submitted.
Publisher:[Australia] : [various publishers], 2013-2014.
Call Numbers:Kibble Awards for Literature 2015
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Books
Food and addiction : a comprehensive handbook / edited by Kelly D. Brownell, Mark S. Gold.
Publisher:Oxford ; New York : Oxford University Press, c2012.
Edition:1st ed.
Call Numbers:G 2013/1727
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Manuscripts | Pictures | Non-Musical Sound Recordings
Len Fox papers, 1852-2001
Author / Creator:Fox, Len, 1905-2004
Date:1852-2001
Call Numbers:MLMSS 8085
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ArticlesPeer ReviewedFull Text
CRISPR-Cas9 interrogation of a putative fetal globin repressor in human erythroid cells
Author / Creator:Chung, Jennifer E. ; Magis, Wendy ; Vu, Jonathan ; Heo, Seok-Jin ; Wartiovaara, Kirmo ; Walters, Mark C. ; Kurita, Ryo ; Nakamura, Yukio ; Boffelli, Dario ; Martin, David I. K. ; Corn, Jacob E. ; DeWitt, Mark A.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2019-01, Vol.14 (1), p.e0208237-e0208237
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ArticlesPeer ReviewedFull Text
2017 Thank you to our reviewers
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2018-04, Vol.55 (4), p.e1-e1
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Newsletter articlesFull Text
Rallybio (RLYB: $6.13) jumps 5.0%, Director Chung Wendy awarded shares
Publisher:Melbourne: News Bites Pty Ltd
Journal title:News Bites US - NASDAQ, 2023
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ArticlesPeer ReviewedFull Text
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
Author / Creator:Miller, David T. ; Lee, Kristy ; Chung, Wendy K. ; Gordon, Adam S. ; Herman, Gail E. ; Klein, Teri E. ; Stewart, Douglas R. ; Amendola, Laura M. ; Adelman, Kathy ; Bale, Sherri J. ; Gollob, Michael H. ; Harrison, Steven M. ; Hershberger, Ray E. ; McKelvey, Kent ; Richards, C. Sue ; Vlangos, Christopher N. ; Watson, Michael S. ; Martin, Christa Lese
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-08, Vol.23 (8), p.1381-1390
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ArticlesPeer ReviewedFull Text
MVP predicts the pathogenicity of missense variants by deep learning
Author / Creator:Qi, Hongjian ; Zhang, Haicang ; Zhao, Yige ; Chen, Chen ; Long, John J. ; Chung, Wendy K. ; Guan, Yongtao ; Shen, Yufeng
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2021-01, Vol.12 (1), p.510-9, Article 510
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ArticlesPeer ReviewedFull Text
Clinical application of whole-exome sequencing across clinical indications
Author / Creator:Retterer, Kyle ; Juusola, Jane ; Cho, Megan T. ; Vitazka, Patrik ; Millan, Francisca ; Gibellini, Federica ; Vertino-Bell, Annette ; Smaoui, Nizar ; Neidich, Julie ; Monaghan, Kristin G. ; McKnight, Dianalee ; Bai, Renkui ; Suchy, Sharon ; Friedman, Bethany ; Tahiliani, Jackie ; Pineda-Alvarez, Daniel ; Richard, Gabriele ; Brandt, Tracy ; Haverfield, Eden ; Chung, Wendy K. ; Bale, Sherri
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2016-07, Vol.18 (7), p.696-704
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ArticlesPeer ReviewedFull Text
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
Author / Creator:Kalia, Sarah S. ; Adelman, Kathy ; Bale, Sherri J. ; Chung, Wendy K. ; Eng, Christine ; Evans, James P. ; Herman, Gail E. ; Hufnagel, Sophia B. ; Klein, Teri E. ; Korf, Bruce R. ; McKelvey, Kent D. ; Ormond, Kelly E. ; Richards, C. Sue ; Vlangos, Christopher N. ; Watson, Michael ; Martin, Christa L. ; Miller, David T.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2017-02, Vol.19 (2), p.249-255
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ArticlesPeer ReviewedFull Text
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
Author / Creator:Miller, David T. ; Lee, Kristy ; Gordon, Adam S. ; Amendola, Laura M. ; Adelman, Kathy ; Bale, Sherri J. ; Chung, Wendy K. ; Gollob, Michael H. ; Harrison, Steven M. ; Herman, Gail E. ; Hershberger, Ray E. ; Klein, Teri E. ; McKelvey, Kent ; Richards, C. Sue ; Vlangos, Christopher N. ; Stewart, Douglas R. ; Watson, Michael S. ; Martin, Christa Lese
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-08, Vol.23 (8), p.1391-1398
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ArticlesPeer ReviewedFull Text
The Congenital Heart Disease Genetic Network Study: Cohort description
Author / Creator:Hoang, Thanh T. ; Goldmuntz, Elizabeth ; Roberts, Amy E. ; Chung, Wendy K. ; Kline, Jennie K. ; Deanfield, John E. ; Giardini, Alessandro ; Aleman, Adolfo ; Gelb, Bruce D. ; Mac Neal, Meghan ; Porter, George A. ; Kim, Richard ; Brueckner, Martina ; Lifton, Richard P. ; Edman, Sharon ; Woyciechowski, Stacy ; Mitchell, Laura E. ; Agopian, A. J.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2018-01, Vol.13 (1), p.e0191319
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ArticlesPeer ReviewedFull Text
Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG)
Author / Creator:Deignan, Joshua L. ; Chung, Wendy K. ; Kearney, Hutton M. ; Monaghan, Kristin G. ; Rehder, Catherine W. ; Chao, Elizabeth C.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2019-06, Vol.21 (6), p.1267-1270
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ArticlesPeer ReviewedFull Text
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders
Author / Creator:Qi, Hongjian ; Yu, Lan ; Zhou, Xueya ; Wynn, Julia ; Zhao, Haoquan ; Guo, Yicheng ; Zhu, Na ; Kitaygorodsky, Alexander ; Hernan, Rebecca ; Aspelund, Gudrun ; Lim, Foong-Yen ; Crombleholme, Timothy ; Cusick, Robert ; Azarow, Kenneth ; Danko, Melissa E. ; Chung, Dai ; Warner, Brad W. ; Mychaliska, George B. ; Potoka, Douglas ; Wagner, Amy J. ; ElFiky, Mahmoud ; Wilson, Jay M. ; Nickerson, Debbie ; Bamshad, Michael ; High, Frances A. ; Longoni, Mauro ; Donahoe, Patricia K. ; Chung, Wendy K. ; Shen, Yufeng
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2018-12, Vol.14 (12), p.e1007822-e1007822
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ArticlesPeer ReviewedFull Text
The genetic basis of pulmonary arterial hypertension
Author / Creator:Ma, Lijiang ; Chung, Wendy K.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2014-05, Vol.133 (5), p.471-479
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Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Author / Creator:Srivastava, Siddharth ; Love-Nichols, Jamie A. ; Dies, Kira A. ; Ledbetter, David H. ; Martin, Christa L. ; Chung, Wendy K. ; Firth, Helen V. ; Frazier, Thomas ; Hansen, Robin L. ; Prock, Lisa ; Brunner, Han ; Hoang, Ny ; Scherer, Stephen W. ; Sahin, Mustafa ; Miller, David T.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2019-11, Vol.21 (11), p.2413-2421
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ArticlesPeer ReviewedFull Text
Rare variant phasing and haplotypic expression from RNA sequencing with phASER
Author / Creator:Castel, Stephane E. ; Mohammadi, Pejman ; Chung, Wendy K. ; Shen, Yufeng ; Lappalainen, Tuuli
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2016-09, Vol.7 (1), p.12817-6, Article 12817
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Showing 1 to 20 of 498 results

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The impact of cultural differences on an Australian firm doing business in China [electronic resource] / Mona Chung & Wendy Smith.

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Managing academic support for international students [electronic resource] : the appropriateness of a learning support unit in an Australian tertiary institution / Mona Chung, Martin kelliher & Wendy...

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Henry James in context / edited by David McWhirter.

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Kibble Awards for Literature 2015 : entries submitted.

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Food and addiction : a comprehensive handbook / edited by Kelly D. Brownell, Mark S. Gold.

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Len Fox papers, 1852-2001

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CRISPR-Cas9 interrogation of a putative fetal globin repressor in human erythroid cells

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2017 Thank you to our reviewers

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Rallybio (RLYB: $6.13) jumps 5.0%, Director Chung Wendy awarded shares

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ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

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MVP predicts the pathogenicity of missense variants by deep learning

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Clinical application of whole-exome sequencing across clinical indications

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

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The Congenital Heart Disease Genetic Network Study: Cohort description

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Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG)

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De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

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The genetic basis of pulmonary arterial hypertension

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Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

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Rare variant phasing and haplotypic expression from RNA sequencing with phASER

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