Judith St-Onge

Judith St-Onge

UNVERIFIED PROFILE

Are you Judith St-Onge?   Register this Author

Register author
Judith St-Onge

Judith St-Onge

Publications by authors named "Judith St-Onge"

Are you Judith St-Onge?   Register this Author

44Publications

1655Reads

48Profile Views

Helping Bridge the Great Divides: Supporting Nurse Communication at End of Life.

J Christ Nurs 2018 Oct/Dec;35(4):258-262

Sondra B. Lee, DNP, FNP-C, is an oncology nurse practitioner, with 22 years' experience in critical care and education. She is an End-of-Life Nursing Education Consortium Trainer. Jeffery W. Forehand, PhD(c), DNP, RN-BC, CNE, is director and professor at Troy University School of Nursing, Troy, Alabama. Judith L. St. Onge, PhD, RN, has 40 years' experience in military and federal clinical nursing and education. Kristi A. Acker, DNP, RN, serves on the multidisciplinary State Advisory Council on Palliative Care and nationally, on the Hospice and Palliative Nurses Association Graduate Nursing Faculty Advisory Committee.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/CNJ.0000000000000542DOI Listing
September 2019

Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia.

Neurogenetics 2019 05 28;20(2):103-108. Epub 2019 Mar 28.

Departments of Pediatrics, Neurology & Neurosurgery, MUHC-Research Institute, McGill University, 1001 Blvd Décarie, Montreal, H4A 3J1, Canada.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s10048-019-00572-7
Publisher Site
http://dx.doi.org/10.1007/s10048-019-00572-7DOI Listing
May 2019

Reducing diagnostic turnaround times of exome sequencing for families requiring timely diagnoses.

Eur J Med Genet 2017 Nov 12;60(11):595-604. Epub 2017 Aug 12.

Equipe Génétique des Anomalies du Développement, INSERM UMR1231, Université de Bourgogne-Franche Comté, Dijon, France; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, France. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S17697212173019
Publisher Site
http://dx.doi.org/10.1016/j.ejmg.2017.08.011DOI Listing
November 2017

Mosaicism for a KITLG Mutation in Linear and Whorled Nevoid Hypermelanosis.

J Invest Dermatol 2017 07 28;137(7):1575-1578. Epub 2017 Feb 28.

Université Bourgogne Franche-Comté, EA 4271 Génétique des Anomalies du Développement, Dijon, France; Service de Pathologie, Plateau Technique de Biologie, CHU Dijon Bourgogne, France; Service de Dermatologie, CHU Dijon Bourgogne, Dijon, France; Centre de référence Anomalies du Développement et Syndromes Malformatifs, CHU Dijon Bourgogne, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jid.2017.01.035DOI Listing
July 2017

Postzygotic BRAF p.Lys601Asn Mutation in Phacomatosis Pigmentokeratotica with Woolly Hair Nevus and Focal Cortical Dysplasia.

J Invest Dermatol 2016 05 29;136(5):1060-1062. Epub 2016 Jan 29.

Equipe d'Accueil 4271, Génétique des Anomalies du Développement, Université de Bourgogne Franche-Comté, Dijon, France; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Centre Hospitalo-Universitaire Dijon-Bourgogne, Dijon, France; Service de Dermatologie, Centre Hospitalo-Universitaire Dijon-Bourgogne, Dijon, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jid.2016.01.015DOI Listing
May 2016

Mutations in SLC13A5 cause autosomal-recessive epileptic encephalopathy with seizure onset in the first days of life.

Am J Hum Genet 2014 Jul;95(1):113-20

Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (TRANSLAD), Centre Hospitalier Universitaire Dijon, 21079 Dijon, France; Equipe d'Accueil 4271, Génétique des Anomalies du Développement, Université de Bourgogne, 21079 Dijon, France; Laboratoire de Génétique Moléculaire, Plateau Technique de Biologie, Centre Hospitalier Universitaire Dijon, 21079 Dijon, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2014.06.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085634PMC
July 2014

An innovative tool for experiential learning of nursing quality and safety competencies.

Nurse Educ 2013 Mar-Apr;38(2):71-5

School of Nursing, Troy University, Montgomery, Alabama 36104, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/NNE.0b013e3182829c7dDOI Listing
April 2013

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.

J Hum Genet 2011 Mar 16;56(3):247-9. Epub 2010 Dec 16.

Center of Excellence in Neuromics of Université de Montréal, CHUM Research Center, Montreal, Quebec, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/jhg.2010.162DOI Listing
March 2011

Genome-wide TDT analysis in French-Canadian families with Tourette syndrome.

Can J Neurol Sci 2010 Jan;37(1):110-2

The Centre of Excellence in Neuromics, CHUM Research Center Department of Medicine, University of Montreal, Montreal, Quebec, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/s0317167100009744DOI Listing
January 2010

Association of intronic variants of the BTBD9 gene with Tourette syndrome.

Arch Neurol 2009 Oct;66(10):1267-72

Sainte Justine Hospital Research Center and the Center of Excellence in Neuromics, University of Montreal, Montreal, QC H2L 4M1, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneurol.2009.213DOI Listing
October 2009

Novel de novo SHANK3 mutation in autistic patients.

Am J Med Genet B Neuropsychiatr Genet 2009 Apr;150B(3):421-4

Centre of Excellence in Neuromics of Université de Montréal, CHUM Research Centre, Notre-Dame Hospital, Université de Montréal, Montreal, QC, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.b.30822DOI Listing
April 2009

A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.

Arch Neurol 2008 Nov;65(11):1496-501

Centre of Excellence in Neuromics, Centre Hospitalier de l'Université de Montreal and Ste-Justine Hospital, Montreal, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.65.11.1496DOI Listing
November 2008

Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians.

Sleep Med 2008 Mar 17;9(3):273-82. Epub 2007 Jul 17.

Center for the Study of Brain Diseases, CHUM Research Center - Notre Dame Hospital, University of Montreal, Bureau Y-3616-2, 1560, rue Sherbrooke Est, Montréal, Que., Canada H2L 4MI.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S13899457070012
Publisher Site
http://dx.doi.org/10.1016/j.sleep.2007.03.020DOI Listing
March 2008

Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families.

Am J Med Genet B Neuropsychiatr Genet 2007 Oct;144B(7):911-7

Laboratoire d'étude des maladies du cerveau, Centre de recherche du CHUM, Hôpital Notre-Dame, Université de Montréal, 1560 rue Sherbrooke Est, Montréal, Québec, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.b.30528DOI Listing
October 2007

Additive effects of obesity and TCF7L2 variants on risk for type 2 diabetes among cardiac patients.

Diabetes Care 2007 Jun 10;30(6):1621-3. Epub 2007 Mar 10.

Department of Medicine, Université de Montréal and Centre Hospitalier de l'Université de Montréal, Montréal, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2337/dc06-2421DOI Listing
June 2007

SPG4 founder effect in French Canadians with hereditary spastic paraplegia.

Can J Neurol Sci 2007 May;34(2):211-4

Center for the Study of Brain Diseases, CHUM Research Center, Notre-Dame Hospital, Montreal, QC, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/s0317167100006065DOI Listing
May 2007

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.

Am J Med Genet B Neuropsychiatr Genet 2005 Jan;132B(1):74-5

Research Institute of the McGill University, Health Center, Cedar Ave, Montreal, H3G 1A4, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.b.30066DOI Listing
January 2005

CAA insertion polymorphism in the 3'UTR of Nogo gene on 2p14 is not associated with schizophrenia.

Brain Res Mol Brain Res 2005 Jan;133(1):153-6

Department of Psychiatry, Douglas Hospital Research Centre, 6875 Boulevard Lasalle, FBC Pavillion, Verdun, Quebec, Canada H4H1R3.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.molbrainres.2004.08.024DOI Listing
January 2005

The 14q restless legs syndrome locus in the French Canadian population.

Ann Neurol 2004 Jun;55(6):887-91

Centre for Research in Neuroscience, McGill University Health Centre Research Institute, Montreal General Hospital, Quebec, Canada.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ana.20140
Publisher Site
http://dx.doi.org/10.1002/ana.20140DOI Listing
June 2004