FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Chantal Morel

Research Profile

Physiology

Procedures

Chemicals & Drugs

Disorders

Living Beings

Concepts & Ideas

Geographic Areas

Canada

Co-author Network

Publications

TOP 3
Adam Shlien; Berivan Baskin; Maria Isabel W Achatz; Dimitrios J Stavropoulos; Kim E Nichols; Louanne Hudgins; Chantal F Morel; Margaret P Adam; Nataliya Zhukova; Lianne Rotin; Ana Novokmet; Harriet Druker; Mary Shago; Peter N Ray; Pierre Hainaut; David Malkin
A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.
Chai Saechao; Yadira Valles-Ayoub; Saghi Esfandiarifard; Arman Haghighatgoo; Daniel No; Steven Shook; Jerry R Mendell; XIOMARA QUINTERO ROSALES; Kevin J Felice; Chantal F Morel; Marvin Pietruska; Daniel Darvish
Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent.
Elaine Suk-Ying Goh; Chumei Li; Sheri Horsburgh; Yumi Kasai; Elena Kolomietz; Chantal F Morel
The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Chantal Morel (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2010: Adam Shlien; Berivan Baskin; Maria Isabel W Achatz; Dimitrios J Stavropoulos; Kim E Nichols; Louanne Hudgins; Chantal F Morel; Margaret P Adam; Nataliya Zhukova; Lianne Rotin; Ana Novokmet; Harriet Druker; Mary Shago; Peter N Ray; Pierre Hainaut; David Malkin
A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.
American journal of human genetics 2010;87(5):631-42.
2010: Chai Saechao; Yadira Valles-Ayoub; Saghi Esfandiarifard; Arman Haghighatgoo; Daniel No; Steven Shook; Jerry R Mendell; XIOMARA QUINTERO ROSALES; Kevin J Felice; Chantal F Morel; Marvin Pietruska; Daniel Darvish
Novel GNE mutations in hereditary inclusion body myopathy patients of non-Middle Eastern descent.
Genetic testing and molecular biomarkers 2010;14(2):157-62.
2010: Elaine Suk-Ying Goh; Chumei Li; Sheri Horsburgh; Yumi Kasai; Elena Kolomietz; Chantal F Morel
The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature.
American journal of medical genetics. Part A 2010;152A(2):472-8.
2009: Klaus G E Werner; Chantal F Morel; Adam Kirton; Susanne M Benseler; John M Shoffner; Jane B L Addis; Brian H Robinson; Delilah M Burrowes; Susan I Blaser; Leon G Epstein; Annette Feigenbaum
Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.
Pediatric neurology 2009;41(1):27-33.
2009: Jordan P Lerner-Ellis; Natascia Anastasio; Junhui Liu; David Coelho; Terttu Suormala; Martin Stucki; Amanda D Loewy; Scott Gurd; Elin Grundberg; Chantal F Morel; David Watkins; Matthias R Baumgartner; Tomi Pastinen; David S Rosenblatt; Brian Fowler
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
Human mutation 2009;30(7):1072-81.
2009: Chantal F Morel; Joe Clarke
The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry disease.
Expert opinion on biological therapy 2009;9(5):631-9.
2007: Anne Chun-Hui Tsai; Chantal F Morel; Gunter Scharer; Michael Yang; Jordan P Lerner-Ellis; David S Rosenblatt; Janet A Thomas
Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance.
American journal of medical genetics. Part A 2007;143A(20):2430-4.
2006: Chantal F Morel; Jordan P Lerner-Ellis; David S Rosenblatt
Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations.
Molecular genetics and metabolism 2006;88(4):315-21.
2006: Chantal F Morel; Mary Ann Thomas; Henian Cao; Caroline O'Neil; J Geoffrey Pickering; William D Foulkes; Robert A Hegele
A LMNA splicing mutation in two sisters with severe Dunnigan-type familial partial lipodystrophy type 2.
The Journal of clinical endocrinology and metabolism 2006;91(7):2689-95.
2006: Jordan P Lerner-Ellis; Jamie C Tirone; Peter D Pawelek; Carole Doré; Janet L Atkinson; David Watkins; Chantal F Morel; T Mary Fujiwara; Emily Moras; Angela Hosack; Gail V Dunbar; Hana Antonicka; Vince Forgetta; C Melissa Dobson; Daniel Leclerc; Roy A Gravel; Eric A Shoubridge; James W Coulton; Pierre Lepage; Johanna M Rommens; Kenneth Morgan; David S Rosenblatt
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Nature genetics 2006;38(1):93-100.
2005: Chantal F Morel; David Watkins; patrick scott; Piero Rinaldo; David S Rosenblatt
Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.
Molecular genetics and metabolism 2005;86(1-2):160-71.
2005: Chantal F Morel; patrick scott; Ernst Christensen; David S Rosenblatt; Rima Rozen
Prenatal diagnosis for severe methylenetetrahydrofolate reductase deficiency by linkage analysis and enzymatic assay.
Molecular genetics and metabolism 2005;85(2):115-20.
2005: Chantal F Morel; Alessandra M V Duncan; Valérie Désilets
A fragile site at 10q23 (FRA10A) in a phenytoin-exposed fetus: a case report and review of the literature.
Prenatal diagnosis 2005;25(4):318-21.