Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mike Kadour"'
Autor:
Ana Cabrera, Fatimah Al Mutawah, Mike Kadour, Shannon Schofield, Beverley Conkey, Jeffrey Fuller, Michael Payne, Sameer Elsayed, Johan Delport
Publikováno v:
PLoS ONE, Vol 18, Iss 6, p e0267137 (2023)
Innovation in laboratory testing algorithms to address seemingly uncontrollable global supply chain shortages in plastics and other consumables during emergencies such as the current COVID-19 pandemic have been urgently needed. We report our experien
Externí odkaz:
https://doaj.org/article/0b0c6a45709b42afa4be75a85bf7d52e
Autor:
Pratibha Bhai, Michael A. Levy, Kathleen Rooney, Deanna Alexis Carere, Jack Reilly, Jennifer Kerkhof, Michael Volodarsky, Alan Stuart, Mike Kadour, Karen Panabaker, Laila C. Schenkel, Hanxin Lin, Peter Ainsworth, Bekim Sadikovic
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
BackgroundHereditary cancer predisposition syndromes account for approximately 10% of cancer cases. Next generation sequencing (NGS) based multi-gene targeted panels is now a frontline approach to identify pathogenic mutations in cancer predispositio
Externí odkaz:
https://doaj.org/article/22fc06b1488549319e08328937c5ba16
Autor:
Benjamin Chin-Yee, Pratibha Bhai, Ian Cheong, Maxim Matyashin, Cyrus C. Hsia, Eri Kawata, Jenny M. Ho, Michael A. Levy, Alan Stuart, Hanxin Lin, Ian Chin-Yee, Mike Kadour, Bekim Sadikovic, Alejandro Lazo-Langner
Publikováno v:
Journal of General Internal Medicine.
Erythrocytosis, most often measured as an increase in hemoglobin and/or hematocrit, is a common reason for referral to internal medicine and hematology clinics and a rational approach is required to effectively identify patients with polycythemia ver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a3e567424d1468902ee7fd8912e7073
https://doi.org/10.1007/s11606-022-07963-x
https://doi.org/10.1007/s11606-022-07963-x
Autor:
Alejandro Lazo-Langner, Ping Yang, Mike Kadour, Benjamin Chin-Yee, Eri Kawata, Kang Howson-Jan, Stephanie Santos, Benjamin D. Hedley, Cyrus C. Hsia, Christopher J. Howlett, Anargyros Xenocostas, Hanxin Lin, Bekim Sadikovic, Ian Chin-Yee, Pratibha Bhai, Michael A. Levy
Publikováno v:
International journal of laboratory hematologyREFERENCES. 44(2)
Introduction In most laboratories, next generation sequencing (NGS) has been added without consideration for redundancy compared to conventional cytogenetics (CG). We tested a streamlined approach to genomic testing in patients with suspected myeloid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e104153d83b2ba7e6a81d6ae9fdf27
https://pubmed.ncbi.nlm.nih.gov/34713980
https://pubmed.ncbi.nlm.nih.gov/34713980
Autor:
Steven A. Skinner, Jennefer Masters, Victoria Mok Siu, Peter Henneman, Jennifer A. Lee, Jorge L. Granadillo, Haley McConkey, Erfan Aref-Eshghi, Mike Kadour, Robin S. Fletcher, Barbara R. DuPont, Alan Stuart, Michael A. Levy, Tugce B. Balci, Michael J. Friez, Bekim Sadikovic, Marielle Alders, Mieke M. van Haelst, Matthew L. Tedder, Roger E. Stevenson, Raymond J. Louie, Charles E. Schwartz, Marcel M.A.M. Mannens, Laila C. Schenkel, Andrea Venema, Jennifer Kerkhof
Publikováno v:
Sadikovic, B, Levi, M A, Kerkhof, J, Aref-Eshghi, E, Schenkel, L, Stuart, A, McConkey, H, Henneman, P, Venema, A, Schwartz, C E, Stevenson, R E, Skinner, S A, DuPont, B R, Fletcher, R S, Balci, T B, Siu, V M, Granadillo, J L, Masters, J, Kadour, M, Friez, M J, van Haelst, M M, Mannens, M M A M, Louie, R J, Lee, J A, Tedder, M L & Alders, M 2021, ' Clinical epigenomics : genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders ', Genetics in Medicine, vol. 23, no. 6, pp. 1065-1074 . https://doi.org/10.1038/s41436-020-01096-4
Genetics in Medicine
Paediatrics Publications
Genetics in Medicine, 23(6), 1065-1074. Lippincott Williams and Wilkins
Genetics in medicine, 23(6), 1065-1074. Lippincott Williams and Wilkins
Genetics in Medicine
Paediatrics Publications
Genetics in Medicine, 23(6), 1065-1074. Lippincott Williams and Wilkins
Genetics in medicine, 23(6), 1065-1074. Lippincott Williams and Wilkins
Purpose: We describe the clinical implementation of genome-wide DNA methylation analysis in rare disorders across the EpiSign diagnostic laboratory network and the assessment of results and clinical impact in the first subjects tested. Methods: We ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7642e4cb481c6146ecedf9aa71c123e
https://pubmed.ncbi.nlm.nih.gov/33637969
https://pubmed.ncbi.nlm.nih.gov/33637969
Autor:
Julien Van-Gils, Kyoko Takano, Victor P. Pedro, Lauren Brick, Pascale Saugier-Veber, Tugce B. Balci, Antonio Vitobello, Marielle Alders, Justine Rousseau, Frédéric Laumonnier, Christel Thauvin-Robinet, Raoul C.M. Hennekam, Tjitske Kleefstra, Matt Tedder, Jennifer Kerkhof, Damien Sanlaville, Gaël Nicolas, François Lecoquierre, Delphine Héron, Hanxin Lin, Sophie Rondeau, Mariya Kozenko, Simone Pizzi, Alexandra Afenjar, Victoria Mok Siu, Christèle Dubourg, David Geneviève, Erfan Aref-Eshghi, Solveig Heide, Barbara R. DuPont, Peter Ainsworth, David I. Rodenhiser, Boris Keren, Nicole de Leeuw, Sandra Whalen, Martine Raynaud, Damien Ulveling, Nathalie Ruiz-Pallares, Valérie Cormier-Daire, Mouna Barat-Houari, Michael A. Levy, Roger E. Stevenson, Jennifer A. Lee, Steven A. Skinner, Alan Graham Stuart, Laurence Faivre, Marie Shaw, Gaetan Lesca, Peter Henneman, Thierry Bienvenu, Marco Tartaglia, Charles E. Schwartz, Andrea Ciolfi, Michael J. Friez, Michael Field, Mike Kadour, Guillaume Velasco, Jozef Gecz, Claire Francastel, Didier Lacombe, Philippe M. Campeau, Jean-Christophe Andrau, Bekim Sadikovic, Marcel M.A.M. Mannens, Jennifer Masters, Cyril Mignot, Patricia Fergelot, Nicolas Chatron
Publikováno v:
American journal of human genetics, 106(3), 356-370. Cell Press
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2020, 106 (3), pp.356-370. ⟨10.1016/j.ajhg.2020.01.019⟩
American Journal of Human Genetics, 2020, 106 (3), pp.356-370. ⟨10.1016/j.ajhg.2020.01.019⟩
Am J Hum Genet
Paediatrics Publications
American Journal of Human Genetics, 106, 3, pp. 356-370
American Journal of Human Genetics, 106, 356-370
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2020, 106 (3), pp.356-370. ⟨10.1016/j.ajhg.2020.01.019⟩
American Journal of Human Genetics, 2020, 106 (3), pp.356-370. ⟨10.1016/j.ajhg.2020.01.019⟩
Am J Hum Genet
Paediatrics Publications
American Journal of Human Genetics, 106, 3, pp. 356-370
American Journal of Human Genetics, 106, 356-370
Contains fulltext : 218274.pdf (Publisher’s version ) (Closed access) Genetic syndromes frequently present with overlapping clinical features and inconclusive or ambiguous genetic findings which can confound accurate diagnosis and clinical manageme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd1d24b3fed514c0a55ce16403898b8f
https://pure.amc.nl/en/publications/evaluation-of-dna-methylation-episignatures-for-diagnosis-and-phenotype-correlations-in-42-mendelian-neurodevelopmental-disorders(fa9b6ccc-bdc4-4b90-a7d5-976a329b9fab).html
https://pure.amc.nl/en/publications/evaluation-of-dna-methylation-episignatures-for-diagnosis-and-phenotype-correlations-in-42-mendelian-neurodevelopmental-disorders(fa9b6ccc-bdc4-4b90-a7d5-976a329b9fab).html
Autor:
Maxim Matyashin, Mike Kadour, Pratibha Bhai, Alejandro Lazo-Langner, Benjamin Chin-Yee, Eri Kawata, Bekim Sadikovic, Hanxin Lin, Ian Cheong, Ian Chin-Yee, Cyrus C. Hsia, Jenny M. Ho
Publikováno v:
Blood. 138:4635-4635
Background: The widespread availability of molecular testing for JAK2 mutations has facilitated the diagnosis of polycythemia vera (PV) but also raises the concern of test overutilization in patients referred for elevated hemoglobin. At our instituti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7795a878635e4e3fcc6c50b2d0d6dca
https://doi.org/10.1182/blood-2021-149241
https://doi.org/10.1182/blood-2021-149241
Autor:
Charles E. Schwartz, Peter Henneman, Barbara R. DuPont, Mike Kadour, Bekim Sadikovic, Erfan Aref-Eshghi, Marcel M.A.M. Mannens, Haley McConkey, Victoria Mok Siu, Roger E. Stevenson, Tugce B. Balci, Alan Stuart, Matthew L. Tedder, Jennifer Kerkhof, Laila C. Schenkel, Andrea Venema, Michael J. Friez, Jorge L. Granadillo, Mieke M. van Haelst, Michael A. Levy, Marielle Alders, Jennifer A. Lee, Robin S. Fletcher, Steven A. Skinner, Jennefer Masters, Raymond J. Louie
Publikováno v:
Genetics in Medicine. 23:2228
The original version of this article unfortunately contained a mistake. The following correction has therefore been made in the original: The spelling of Michael A. Levy’s name was incorrect. The corrected author list is given above. The original a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7ac066202ab6d4088603b374b84aace
https://doi.org/10.1038/s41436-021-01130-z
https://doi.org/10.1038/s41436-021-01130-z
Publikováno v:
CMAJ : Canadian Medical Association Journal
Wang and colleagues provided valuable insight into the impact of coronavirus disease 2019 (COVID-19), estimating a backlog of 148 364 surgeries in Ontario from March to June 2020.[1][1] Expanding on the issues they raised, we would like to highlight
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a82870bcc9380ba0d5f27ec13416406
https://doi.org/10.1503/cmaj.77883
https://doi.org/10.1503/cmaj.77883
Autor:
Cabrera, Ana1,2,3 (AUTHOR) ana.cabrera@lhsc.on.ca, Al Mutawah, Fatimah1,2 (AUTHOR), Kadour, Mike1,2 (AUTHOR), Schofield, Shannon1 (AUTHOR), Conkey, Beverley1 (AUTHOR), Fuller, Jeffrey1,2 (AUTHOR), Payne, Michael1,2 (AUTHOR), Elsayed, Sameer1,2,4,5 (AUTHOR), Delport, Johan1,2,3 (AUTHOR)
Publikováno v:
PLoS ONE. 6/28/2023, Vol. 17 Issue 6, p1-13. 13p.