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52 results for Ware,+Stephanie+M

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Books
A catalogue of above fifteen thousand volumes, [electronic resource] : In all Arts, Sciences, and every Branch of polite Literature, Many on Royal Paper, and in Morocco, and other elegant Bindings; be...
Author / Creator:Hinxman, J., -1762.
Publisher:[York? : s.n., 1759]
Date:1759]
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Manuscripts
Edward St. John - correspondence, 1974-1994
Call Numbers:MLMSS 6660/1-5
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Books
Women : a feminist perspective / edited by Jo Freeman.
Publisher:Mountain View, Calif. : Mayfield Pub. Co., c1995.
Edition:5th ed.
Call Numbers:G 2013/1932
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Manuscripts
Boxes 61-80: Allen & Unwin further records
Call Numbers:MLMSS 7981/Boxes 61-80
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Manuscripts | Drawings | Photographs
Series 01 Part 03: Allen & Unwin Production files. F Sequence, ca. 1987-1993
Date:1987-1993
Call Numbers:MLMSS 6686/Boxes 61-90
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Reference EntriesFull Text
Ware, Stephanie M
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: TRA-WID, 2022, p.12023-12023
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Reference EntriesFull Text
Ware, Stephanie M
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: TRO-WIK, 2021, p.11991-11991
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ArticlesPeer ReviewedFull Text
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline
Author / Creator:Shapiro, Adam J. ; Davis, Stephanie D. ; Polineni, Deepika ; Manion, Michele ; Rosenfeld, Margaret ; Dell, Sharon D. ; Chilvers, Mark A. ; Ferkol, Thomas W. ; Zariwala, Maimoona A. ; Sagel, Scott D. ; Josephson, Maureen ; Morgan, Lucy ; Yilmaz, Ozge ; Olivier, Kenneth N. ; Milla, Carlos ; Pittman, Jessica E. ; Daniels, M. Leigh Anne ; Jones, Marcus Herbert ; Janahi, Ibrahim A. ; Ware, Stephanie M. ; Daniel, Sam J. ; Cooper, Matthew L. ; Nogee, Lawrence M. ; Anton, Billy ; Eastvold, Tori ; Ehrne, Lynn ; Guadagno, Elena ; Knowles, Michael R. ; Leigh, Margaret W. ; Lavergne, Valery
Publisher:United States: American Thoracic Society
Journal title:American journal of respiratory and critical care medicine, 2018-06, Vol.197 (12), p.e24-e39
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ArticlesPeer ReviewedFull Text
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Author / Creator:Hershberger, Ray E. ; Givertz, Michael M. ; Ho, Carolyn Y ; Judge, Daniel P. ; Kantor, Paul F. ; McBride, Kim L. ; Morales, Ana ; Taylor, Matthew R. G. ; Vatta, Matteo ; Ware, Stephanie M.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2018-09, Vol.20 (9), p.899-909
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ArticlesPeer ReviewedFull Text
Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes
Author / Creator:Bellchambers, Helen M. ; Phatak, Amruta R. ; Nenni, Mardi J. ; Padua, Maria B. ; Gao, Hongyu ; Liu, Yunlong ; Ware, Stephanie M.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2023-07, Vol.13 (1), p.10688-12, Article 10688
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ArticlesPeer ReviewedFull Text
Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
Author / Creator:Fakhro, Khalid A. ; Choi, Murim ; Ware, Stephanie M. ; Belmont, John W. ; Towbin, Jeffrey A. ; Lifton, Richard P. ; Khokha, Mustafa K. ; Brueckner, Martina
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (7), p.2915-2920
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ArticlesPeer ReviewedFull Text
Genetic architecture of laterality defects revealed by whole exome sequencing
Author / Creator:Li, Alexander H ; Hanchard, Neil A ; Azamian Mahshid ; D’Alessandro Lisa C A ; Coban-Akdemir Zeynep ; Lopez, Keila N ; Hall, Nancy J ; Dickerson, Heather ; Nicosia Annarita ; Fernbach, Susan ; Boone, Philip M ; Gambin Tomaz ; Karaca Ender ; Gu, Shen ; Yuan, Bo ; Jhangiani, Shalini N ; Doddapaneni HarshaVardhan ; Hu, Jianhong ; Dinh Huyen ; Jayaseelan Joy ; Muzny Donna ; Lalani Seema ; Towbin, Jeffrey ; Penny, Daniel ; Fraser, Charles ; Martin, James ; Lupski James R ; Gibbs, Richard A ; Boerwinkle, Eric ; Ware, Stephanie M ; Belmont, John W
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2019-04, Vol.27 (4), p.563-573
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ArticlesPeer ReviewedFull Text
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
Author / Creator:Li, You ; Yagi, Hisato ; Onuoha, Ezenwa Obi ; Damerla, Rama Rao ; Francis, Richard ; Furutani, Yoshiyuki ; Tariq, Muhammad ; King, Stephen M. ; Hendricks, Gregory ; Cui, Cheng ; Saydmohammed, Manush ; Lee, Dong Min ; Zahid, Maliha ; Sami, Iman ; Leatherbury, Linda ; Pazour, Gregory J. ; Ware, Stephanie M. ; Nakanishi, Toshio ; Goldmuntz, Elizabeth ; Tsang, Michael ; Lo, Cecilia W.
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2016-02, Vol.12 (2), p.e1005821
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ArticlesPeer ReviewedFull Text
Evaluation of genetic causes of cardiomyopathy in childhood
Author / Creator:Ware, Stephanie M.
Publisher:Cambridge, UK: Cambridge University Press
Journal title:Cardiology in the young, 2015-08, Vol.25 (S2), p.43-50
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ArticlesPeer ReviewedFull Text
A multi-disciplinary, comprehensive approach to management of children with heterotaxy
Author / Creator:Saba, Thomas G. ; Geddes, Gabrielle C. ; Ware, Stephanie M. ; Schidlow, David N. ; del Nido, Pedro J. ; Rubalcava, Nathan S. ; Gadepalli, Samir K. ; Stillwell, Terri ; Griffiths, Anne ; Bennett Murphy, Laura M. ; Barber, Andrew T. ; Leigh, Margaret W. ; Sabin, Necia ; Shapiro, Adam J.
Publisher:London: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2022-09, Vol.17 (1), p.1-17, Article 351
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ArticlesPeer ReviewedFull Text
Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative Genomics
Author / Creator:Rindler, Tara N. ; Hinton, Robert B. ; Salomonis, Nathan ; Ware, Stephanie M.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-01, Vol.7 (1), p.39276-39276, Article 39276
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ArticlesPeer ReviewedFull Text
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
Author / Creator:Tariq, Muhammad ; Belmont, John W ; Lalani, Seema ; Smolarek, Teresa ; Ware, Stephanie M
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology (Online Edition), 2011-09, Vol.12 (9), p.R91-2688, Article R91
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ArticlesPeer ReviewedFull Text
Performance of Dysmorphology‐Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Author / Creator:Helm, Benjamin M. ; Helvaty, Lindsey R. ; Conboy, Erin ; Geddes, Gabrielle C. ; Graham, Brett H. ; Lah, Melissa ; Wetherill, Leah ; Landis, Benjamin J. ; Ware, Stephanie M.
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2024-11, Vol.12 (11), p.e70040-n/a
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ArticlesPeer ReviewedFull Text
Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging
Author / Creator:Tandon, Animesh, MD, MS ; Jefferies, John L., MD, MPH ; Villa, Chet R., MD ; Hor, Kan N., MD ; Wong, Brenda L., MD ; Ware, Stephanie M., MD, PhD ; Gao, Zhiqian, PhD ; Towbin, Jeffrey A., MD, MS ; Mazur, Wojciech, MD ; Fleck, Robert J., MD ; Sticka, Joshua J., MD ; Benson, D. Woodrow, MD, PhD ; Taylor, Michael D., MD, PhD
Publisher:United States: Elsevier Inc
Journal title:The American journal of cardiology, 2015-04, Vol.115 (7), p.967-971
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ArticlesPeer ReviewedFull Text
Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease
Author / Creator:Bedard, James E. J. ; Haaning, Allison M. ; Ware, Stephanie M.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2011-08, Vol.6 (8), p.e23755
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A catalogue of above fifteen thousand volumes, [electronic resource] : In all Arts, Sciences, and every Branch of polite Literature, Many on Royal Paper, and in Morocco, and other elegant Bindings; be...

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Edward St. John - correspondence, 1974-1994

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Women : a feminist perspective / edited by Jo Freeman.

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Boxes 61-80: Allen & Unwin further records

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Series 01 Part 03: Allen & Unwin Production files. F Sequence, ca. 1987-1993

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Ware, Stephanie M

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Ware, Stephanie M

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Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline

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Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

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Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes

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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

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Genetic architecture of laterality defects revealed by whole exome sequencing

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DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia

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Evaluation of genetic causes of cardiomyopathy in childhood

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A multi-disciplinary, comprehensive approach to management of children with heterotaxy

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Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative Genomics

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SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

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Performance of Dysmorphology‐Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing

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Dystrophin Genotype–Cardiac Phenotype Correlations in Duchenne and Becker Muscular Dystrophies Using Cardiac Magnetic Resonance Imaging

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Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease

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