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Search Results - Wilde, Melanie E.
Search Results - Wilde, Melanie E.
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Developing the communicative competence and narrative thinking of four and five year olds in educational settings
by
Wilde, Melanie E.
,
Sage, Rosemary
Published in
Early child development and care
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An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome
by
Adler, Arnon
,
Novelli, Valeria
,
Amin, Ahmad S.
,
Abiusi, Emanuela
,
Care, Melanie
,
Nannenberg, Eline A.
,
Feilotter, Harriet
,
Amenta, Simona
,
Mazza, Daniela
,
Bikker, Hennie
,
Sturm, Amy C.
,
Garcia, John
,
Ackerman, Michael J.
,
Hershberger, Raymond E.
,
Perez, Marco V.
,
Zareba, Wojciech
,
Ware, James S.
,
Wilde, Arthur A.M.
,
Gollob, Michael H.
Published in
Circulation (New York, N.Y.)
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Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome
by
Hosseini, S Mohsen
,
Kim, Raymond
,
Udupa, Sharmila
,
Costain, Gregory
,
Jobling, Rebekah
,
Liston, Eriskay
,
Jamal, Seema M
,
Szybowska, Marta
,
Morel, Chantal F
,
Bowdin, Sarah
,
Garcia, John
,
Care, Melanie
,
Sturm, Amy C
,
Novelli, Valeria
,
Ackerman, Michael J
,
Ware, James S
,
Hershberger, Ray E
,
Wilde, Arthur A.M
,
Gollob, Michael H
Published in
Circulation (New York, N.Y.)
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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
by
Walsh, Roddy
,
Adler, Arnon
,
Amin, Ahmad S
,
Abiusi, Emanuela
,
Care, Melanie
,
Bikker, Hennie
,
Amenta, Simona
,
Feilotter, Harriet
,
Nannenberg, Eline A
,
Mazzarotto, Francesco
,
Trevisan, Valentina
,
Garcia, John
,
Hershberger, Ray E
,
Perez, Marco V
,
Sturm, Amy C
,
Ware, James S
,
Zareba, Wojciech
,
Novelli, Valeria
,
Wilde, Arthur A M
,
Gollob, Michael H
Published in
European heart journal
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An integrated analysis and comparison of serum, saliva and sebum for COVID-19 metabolomics
by
Spick, Matt
,
Lewis, Holly-May
,
Frampas, Cecile F.
,
Longman, Katie
,
Costa, Catia
,
Stewart, Alexander
,
Dunn-Walters, Deborah
,
Greener, Danni
,
Evetts, George
,
Wilde, Michael J.
,
Sinclair, Eleanor
,
Barran, Perdita E.
,
Skene, Debra J.
,
Bailey, Melanie J.
Published in
Scientific reports
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Interlaboratory evaluation of a multiplexed high information content in vitro genotoxicity assay
by
Bryce, Steven M.
,
Bernacki, Derek T.
,
Bemis, Jeffrey C.
,
Spellman, Richard A.
,
Engel, Maria E.
,
Schuler, Maik
,
Lorge, Elisabeth
,
Heikkinen, Pekka T.
,
Hemmann, Ulrike
,
Thybaud, Véronique
,
Wilde, Sabrina
,
Queisser, Nina
,
Sutter, Andreas
,
Zeller, Andreas
,
Guérard, Melanie
,
Kirkland, David
,
Dertinger, Stephen D.
Published in
Environmental and molecular mutagenesis
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HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle
by
Deardorff, Matthew A.
,
Bando, Masashige
,
Nakato, Ryuichiro
,
Watrin, Erwan
,
Itoh, Takehiko
,
Minamino, Masashi
,
Saitoh, Katsuya
,
Komata, Makiko
,
Katou, Yuki
,
Clark, Dinah
,
Cole, Kathryn E.
,
De Baere, Elfride
,
Decroos, Christophe
,
Di Donato, Nataliya
,
Ernst, Sarah
,
Francey, Lauren J.
,
Gyftodimou, Yolanda
,
Hirashima, Kyotaro
,
Hullings, Melanie
,
Ishikawa, Yuuichi
,
Jaulin, Christian
,
Kaur, Maninder
,
Kiyono, Tohru
,
Lombardi, Patrick M.
,
Magnaghi-Jaulin, Laura
,
Mortier, Geert R.
,
Nozaki, Naohito
,
Petersen, Michael B.
,
Seimiya, Hiroyuki
,
Siu, Victoria M.
,
Suzuki, Yutaka
,
Takagaki, Kentaro
,
Wilde, Jonathan J.
,
Willems, Patrick J.
,
Prigent, Claude
,
Gillessen-Kaesbach, Gabriele
,
Christianson, David W.
,
Kaiser, Frank J.
,
Jackson, Laird G.
,
Hirota, Toru
,
Krantz, Ian D.
,
Shirahige, Katsuhiko
Published in
Nature (London)
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Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac condition...
by
Josephs, Katherine S
,
Roberts, Angharad M
,
Theotokis, Pantazis
,
Walsh, Roddy
,
Ostrowski, Philip J
,
Edwards, Matthew
,
Fleming, Andrew
,
Thaxton, Courtney
,
Roberts, Jason D
,
Care, Melanie
,
Zareba, Wojciech
,
Adler, Arnon
,
Sturm, Amy C
,
Tadros, Rafik
,
Novelli, Valeria
,
Owens, Emma
,
Bronicki, Lucas
,
Jarinova, Olga
,
Callewaert, Bert
,
Peters, Stacey
,
Lumbers, Tom
,
Jordan, Elizabeth
,
Asatryan, Babken
,
Krishnan, Neesha
,
Hershberger, Ray E
,
Chahal, C Anwar A
,
Landstrom, Andrew P
,
James, Cynthia
,
McNally, Elizabeth M
,
Judge, Daniel P
,
van Tintelen, Peter
,
Wilde, Arthur
,
Gollob, Michael
,
Ingles, Jodie
,
Ware, James S
Published in
Genome medicine
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
by
Kaiser, Frank J.
,
Ansari, Morad
,
Braunholz, Diana
,
Concepción Gil-Rodríguez, María
,
Decroos, Christophe
,
Wilde, Jonathan J.
,
Fincher, Christopher T.
,
Kaur, Maninder
,
Bando, Masashige
,
Amor, David J.
,
Atwal, Paldeep S.
,
Bahlo, Melanie
,
Bowman, Christine M.
,
Bradley, Jacquelyn J.
,
Brunner, Han G.
,
Clark, Dinah
,
Del Campo, Miguel
,
Di Donato, Nataliya
,
Diakumis, Peter
,
Dubbs, Holly
,
Dyment, David A.
,
Eckhold, Juliane
,
Ernst, Sarah
,
Ferreira, Jose C.
,
Francey, Lauren J.
,
Gehlken, Ulrike
,
Guillén-Navarro, Encarna
,
Gyftodimou, Yolanda
,
Hall, Bryan D.
,
Hennekam, Raoul
,
Hudgins, Louanne
,
Hullings, Melanie
,
Hunter, Jennifer M.
,
Yntema, Helger
,
Innes, A. Micheil
,
Kline, Antonie D.
,
Krumina, Zita
,
Lee, Hane
,
Leppig, Kathleen
,
Lynch, Sally Ann
,
Mallozzi, Mark B.
,
Mannini, Linda
,
Mckee, Shane
,
Mehta, Sarju G.
,
Micule, Ieva
,
Mohammed, Shehla
,
Moran, Ellen
,
Mortier, Geert R.
,
Moser, Joe-Ann S.
,
Noon, Sarah E.
,
Nozaki, Naohito
,
Nunes, Luis
,
Pappas, John G.
,
Penney, Lynette S.
,
Pérez-Aytés, Antonio
,
Petersen, Michael B.
,
Puisac, Beatriz
,
Revencu, Nicole
,
Roeder, Elizabeth
,
Saitta, Sulagna
,
Scheuerle, Angela E.
,
Schindeler, Karen L.
,
Siu, Victoria M.
,
Stark, Zornitza
,
Strom, Samuel P.
,
Thiese, Heidi
,
Vater, Inga
,
Willems, Patrick
,
Williamson, Kathleen
,
Wilson, Louise C.
,
Hakonarson, Hakon
,
Quintero-Rivera, Fabiola
,
Wierzba, Jolanta
,
Musio, Antonio
,
Gillessen-Kaesbach, Gabriele
,
Ramos, Feliciano J.
,
Jackson, Laird G.
,
Shirahige, Katsuhiko
,
Pié, Juan
,
Christianson, David W.
,
Krantz, Ian D.
,
Fitzpatrick, David R.
,
Deardorff, Matthew A.
Published in
Human molecular genetics
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Sepsis now a priority: a quality improvement initiative for early sepsis recognition and care
by
MCDONALD, CHRISTINE M.
,
WEST, SARAH
,
DUSHENSKI, DAVID
,
LAPINSKY, STEPHEN E.
,
SOONG, CHRISTINE
,
VAN DEN BROEK, KATE
,
ASHBY, MELANIE
,
WILDE-FRIEL, GILLIAN
,
KAN, CARRIE
,
MCINTYRE, MARK
,
MORRIS, ANDREW
Published in
International journal for quality in health care
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ELISpot assay as a sensitive tool to detect cellular immunity following influenza vaccination in kidney transplant recipients
by
Lindemann, Monika
,
Witzke, Oliver
,
Lütkes, Peter
,
Fiedler, Melanie
,
Kreuzfelder, Ernst
,
Philipp, Thomas
,
Roggendorf, Michael
,
Grosse-Wilde, Hans
Published in
Clinical Immunology
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