Publications by authors named "Dennis Bulman"

Claim this Profile
T
The evolution of health data ecosystems: An international survey.
Jordan P Lerner-Ellis, E Magda Price, Shazia Subhani, Tiffany Boughtwood, Marie-Jo Brion, Dennis Bulman

Am J Hum Genet· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
FGF14 GAA Intronic Expansion in Unsolved Adult-Onset Ataxia in the Care4Rare Canada Consortium.
Alexanne Cuillerier, Giulia F Del Gobbo, Layla Mackay, Erika Wall, Madeline Couse, Dennis E Bulman

Ann Clin Transl Neurol· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Association of Dual-Task Gait Cost and White Matter Hyperintensity Burden Poststroke: Results From the ONDRI.
Frederico Pieruccini-Faria, Benjamin Cornish, Malcolm Binns, Julia Fraser, Seyyed M H Haddad, Dennis Bulman

Neurorehabil Neural Repair· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Alberta Spinal Muscular Atrophy Newborn Screening-Results from Year 1 Pilot Project.
Farshad Niri, Jessie Nicholls, Kelly Baptista Wyatt, Christine Walker, Tiffany Price, Dennis E Bulman

Int J Neonatal Screen· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman-Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding, Dennis E Bulman

Orphanet J Rare Dis· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening.
Christina Blagojevic, Tracy Heung, Mylene Theriault, Aoy Tomita-Mitchell, Pranesh Chakraborty, Dennis E Bulman

CMAJ Open· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Retrospective testing of respiratory specimens for COVID-19 to assess for earlier SARS-CoV-2 infections in Alberta, Canada.
Jamil N Kanji, Mathew Diggle, Dennis E Bulman, Stacey Hume, Sherry Taylor

J Assoc Med Microbiol Infect Dis Can· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Ataxia Telangiectasia Diagnosed on Newborn Screening-Case Cohort of 5 Years' Experience.
Amarilla B Mandola, Brenda Reid, Raga Sirror, Rae Brager, Peter Dent, Dennis E Bulman

Front Immunol· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Case Report of Myoclonus-Dystonia with Isolated Myoclonus Phenotype and Novel Mutation Successfully Treated with Deep Brain Stimulation.
Valentina Besa Lehmann, Marc Rosenbaum, Dennis E Bulman, Tara Read, Leo Verhagen Metman

Neurol Ther· June 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An evaluation of genetic causes and environmental risks for bilateral optic atrophy.
Andrew T Chen, Lauren Brady, Dennis E Bulman, Arun N E Sundaram, Amadeo R Rodriguez

PLoS One· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening.
Kate C Verbeeten, Anne-Marie Lamhonwah, Dennis Bulman, Hanna Faghfoury, P Chakraborty

Mol Genet Metab· March 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Time-dependent decline of T-cell receptor excision circle levels in ZAP-70 deficiency.
Sneha Suresh, Harjit Dadi, Brenda Reid, Linda Vong, Dennis E Bulman

J Allergy Clin Immunol Pract· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort.
Julia N Heighton, Lauren I Brady, Bekim Sadikovic, Dennis E Bulman, Mark A Tarnopolsky

Mitochondrion· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative.
Allison A Dilliott, Emily C Evans, Sali M K Farhan, Mahdi Ghani, Christine Sato, Dennis E Bulman

Can J Neurol Sci· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Effects of fat mass and obesity-associated (FTO) gene polymorphisms on binge eating in women with binge-eating disorder: The moderating influence of attachment style.
Jameason D Cameron, Giorgio A Tasca, Julian Little, Livia Chyurlia, Kerri Ritchie, Dennis E Bulman

Nutrition· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes.
Erfan Aref-Eshghi, Eric G Bend, Rebecca L Hood, Laila C Schenkel, Deanna Alexis Carere, Dennis E Bulman

Nat Commun· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
In reference to should infants who fail their newborn hearing screen undergo cytomegalovirus testing?
Soren Gantt, David M Goldfarb, Francois Dionne, Dennis Bulman, Sara Menlove Doutré

Laryngoscope· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A family segregating lethal neonatal coenzyme Q deficiency caused by mutations in COQ9.
Amanda C Smith, Yoko Ito, Afsana Ahmed, Jeremy A Schwartzentruber, Chandree L Beaulieu, Dennis E Bulman

J Inherit Metab Dis· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
T-cell receptor excision circle levels and safety of paediatric immunization: A population-based self-controlled case series analysis.
Kumanan Wilson, Daniel Rodriguez Duque, Malia S Q Murphy, Steven Hawken, Anne Pham-Huy, Dennis E Bulman

Hum Vaccin Immunother· June 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease.
Allison A Dilliott, Sali M K Farhan, Mahdi Ghani, Christine Sato, Eric Liang, Dennis E Bulman

J Vis Exp· April 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Q
Quantification of DNA in Neonatal Dried Blood Spots by Adenine Tandem Mass Spectrometry.
Danielle Durie, Ed Yeh, Nathan McIntosh, Lawrence Fisher, Dennis E Bulman

Anal Chem· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes.
Erfan Aref-Eshghi, David I Rodenhiser, Laila C Schenkel, Hanxin Lin, Cindy Skinner, Dennis E Bulman

Am J Hum Genet· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy.
Devon L Johnstone, Thi-Tuyet-Mai Nguyen, Yoshiko Murakami, Kristin D Kernohan, Martine Tétreault, Dennis E Bulman

Hum Mol Genet· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
K
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connection.
Lauren Badalato, Sali M K Farhan, Allison A Dilliott, , Dennis E Bulman

Am J Med Genet A· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The defining DNA methylation signature of Floating-Harbor Syndrome.
Rebecca L Hood, Laila C Schenkel, Sarah M Nikkel, Peter J Ainsworth, Guillaume Pare, Dennis E Bulman

Sci Rep· December 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis