نتائج البحث - "Kadour, Mike"

1

Academic Journal

Increasing SARS-CoV-2 testing capacity through specimen pooling: An acute care center experience

المؤلفون: Cabrera, Ana, Al Mutawah, Fatimah, Kadour, Mike, Schofield, Shannon, Conkey, Beverley, Fuller, Jeffrey, Payne, Michael, Elsayed, Sameer, Delport, Johan

المساهمون: Kalendar, Ruslan

المصدر: PLOS ONE ; volume 18, issue 6, page e0267137 ; ISSN 1932-6203

الاتاحة: http://dx.doi.org/10.1371/journal.pone.0267137
https://dx.plos.org/10.1371/journal.pone.0267137

View record in BASE

2

Academic Journal

Clinical epigenomics:genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders

المصدر: 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 ....

الاتاحة: https://research.vumc.nl/en/publications/86dcec88-29b4-4d1c-af83-f94133deb8ea
https://doi.org/10.1038/s41436-020-01096-4
http://www.scopus.com/inward/record.url?scp=85100548502&partnerID=8YFLogxK

View record in BASE

3

Academic Journal

Correction:Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders (Genetics in Medicine, (2021), 23, 6, (1065-1074), 10.1038/s41436-020-01096-4)

المصدر: Sadikovic , B , Levy , 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 ....

Relation: https://research.vumc.nl/en/publications/8e6b35ca-68cc-48af-b3bc-c76a81c621e5

الاتاحة: https://research.vumc.nl/en/publications/8e6b35ca-68cc-48af-b3bc-c76a81c621e5
https://doi.org/10.1038/s41436-021-01130-z
http://www.scopus.com/inward/record.url?scp=85101735206&partnerID=8YFLogxK

View record in BASE

4

Academic Journal

Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach

المؤلفون: Bhai, Pratibha, Levy, Michael A., Rooney, Kathleen, Carere, Deanna Alexis, Reilly, Jack, Kerkhof, Jennifer, Volodarsky, Michael, Stuart, Alan, Kadour, Mike, Panabaker, Karen, Schenkel, Laila C., Lin, Hanxin, Ainsworth, Peter, Sadikovic, Bekim

المصدر: Frontiers in Genetics ; volume 12 ; ISSN 1664-8021

الاتاحة: http://dx.doi.org/10.3389/fgene.2021.698595
https://www.frontiersin.org/articles/10.3389/fgene.2021.698595/full

View record in BASE

5

Academic Journal

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders

المؤلفون: Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., France, Groupe DI, Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, Van-Gils, Julien, Fergelot, Patricia, Dubourg, Christéle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike

المصدر: The American Journal of Human Genetics ; volume 108, issue 6, page 1161-1163 ; ISSN 0002-9297

الاتاحة: https://doi.org/10.1016/j.ajhg.2021.04.022
https://api.elsevier.com/content/article/PII:S0002929721001531?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929721001531?httpAccept=text/plain

View record in BASE

6

Academic Journal

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders

المؤلفون: Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, Van-Gils, Julien, Fergelot, Patricia, Dubourg, Christèle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike, Masters, Jennifer

المساهمون: Amsterdam Reproduction and Development Institute

المصدر: The American Journal of Human Genetics ; volume 106, issue 3, page 356-370 ; ISSN 0002-9297

الاتاحة: http://dx.doi.org/10.1016/j.ajhg.2020.01.019
https://api.elsevier.com/content/article/PII:S0002929720300197?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929720300197?httpAccept=text/plain

View record in BASE

7

Academic Journal

A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study.

المؤلفون: Chin-Yee, Benjamin, Bhai, Pratibha, Cheong, Ian, Matyashin, Maxim, Hsia, Cyrus C., Kawata, Eri, Ho, Jenny M., Levy, Michael A., Stuart, Alan, Lin, Hanxin, Chin-Yee, Ian, Kadour, Mike, Sadikovic, Bekim, Lazo-Langner, Alejandro

المصدر: JGIM: Journal of General Internal Medicine; Jun2023, Vol. 38 Issue 8, p1828-1833, 6p, 1 Diagram, 2 Charts, 1 Graph

مصطلحات موضوعية: BLOOD cell count, ERYTHROCYTES, HEMOGLOBINS, POLYCYTHEMIA vera, INTERNAL medicine

Full Text Finder

8

Academic Journal

A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study

المؤلفون: Chin-Yee, Benjamin, Bhai, Pratibha, Cheong, Ian, Matyashin, Maxim, Hsia, Cyrus C., Kawata, Eri, Ho, Jenny M., Levy, Michael A., Stuart, Alan, Lin, Hanxin, Chin-Yee, Ian, Kadour, Mike, Sadikovic, Bekim, Lazo-Langner, Alejandro

المصدر: Journal of General Internal Medicine ; volume 38, issue 8, page 1828-1833 ; ISSN 0884-8734 1525-1497

الاتاحة: http://dx.doi.org/10.1007/s11606-022-07963-x
https://link.springer.com/content/pdf/10.1007/s11606-022-07963-x.pdf
https://link.springer.com/article/10.1007/s11606-022-07963-x/fulltext.html

View record in BASE

9

Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders (Genetics in Medicine, (2021), 23, 6, (1065-1074), 10.1038/s41436-020-01096-4)

المساهمون: Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Human Genetics, Amsterdam Gastroenterology Endocrinology Metabolism, ACS - Pulmonary hypertension & thrombosis

المصدر: Paediatrics Publications
Genetics in Medicine, 23(11). Lippincott Williams and Wilkins
Sadikovic, B, Levy, 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, ' Correction : Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders (Genetics in Medicine, (2021), 23, 6, (1065-1074), 10.1038/s41436-020-01096-4) ', Genetics in Medicine, vol. 23, no. 11, pp. 2228 . https://doi.org/10.1038/s41436-021-01130-z
Genetics in medicine, 23(11). Lippincott Williams and Wilkins

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::541de192138ffcc363d3d0887c26516a
https://ir.lib.uwo.ca/context/paedpub/article/1740/viewcontent/s41436_021_01130_z.pdf

View record in OpenAIRE

10

Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))

المؤلفون: Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., France, Groupe D. I., Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, van-Gils, Julien, Fergelot, Patricia, Dubourg, Christéle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike, Masters, Jennifer, Takano, Kyoko, Kleefstra, Tjitske, de Leeuw, Nicole, Field, Michael, Shaw, Marie, Gecz, Jozef, Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Friez, Michael J., Tedder, Matt, Lee, Jennifer A., DuPont, Barbara R., Stevenson, Roger E., Skinner, Steven A., Schwartz, Charles E., Genevieve, David, Sadikovic, Bekim

المساهمون: Human Genetics, ACS - Pulmonary hypertension & thrombosis, Amsterdam Reproduction & Development (AR&D), Amsterdam Gastroenterology Endocrinology Metabolism, General Paediatrics, APH - Quality of Care

المصدر: American journal of human genetics, 108(6), 1161-1163. Cell Press

URL الوصول: https://explore.openaire.eu/search/publication?articleId=narcis______::13e4e22928e243ed11ed92a45384c149
https://pure.amc.nl/en/publications/erratum-evaluation-of-dna-methylation-episignatures-for-diagnosis-and-phenotype-correlations-in-42-mendelian-neurodevelopmental-disorders-the-american-journal-of-human-genetics-2020-1063-356370-s0002929720300197-101016jajhg202001019(afdb59ea-f387-4a08-aca7-f040424710e6).html

View record in OpenAIRE