This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of British Columbia directory, so their courses may be missing. Find their university profile.
Research
Latest papers
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD.
Journal of clinical immunology · 2025
DNA methylation differences between cord and adult white blood cells reflect postnatal immune cell maturation.
Communications biology · 2025
Sex-dependent placental methylation quantitative trait loci provide insight into the prenatal origins of childhood onset traits and conditions.
iScience · 2024
Latest funding
- $150,000
Local Computing Infrastructure for Large Scale Genomic Analysis
NSERC · 2020 · Principal investigator
- $1,013,816
Metabolic regulation of immune defenses in newborns
CIHR · 2019 · Co-investigator
- $187,400
Analysis of multiomic Data to Accelerate Personalized health interventions against inhaled Toxicants (ADAPT)
CIHR · 2017 · Co-investigator
61 publications.
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD.
Lu HY, Vaseghi-Shanjani M, Lam AJ, Sharma M, Mohajeri A, Silva LBR, Gillies J, Yang GX, Lin S, Fu MP, Salman A, Rahmanian R, Armstrong L, Halparin J, Yang CL, Chilvers M, Henkelman E, Rehmus W, Morrison D, Setiadi A, Mostafavi S, Kobor MS, Kozak FK, Biggs CM, van Karnebeek C, Hildebrand KJ, Anna Lehman on behalf of the Care4Rare Canada Consortium, Levings MK, Turvey SE
DNA methylation differences between cord and adult white blood cells reflect postnatal immune cell maturation.
Jones MJ, Konwar C, Asiimwe R, Dinh L, Razzaghian HR, de Goede O, MacIsaac JL, Morin AM, Kolsun KP, Gervin K, Lyle R, Ng RT, Koestler DC, Felix JF, Lavoie PM, Robinson WP, Mostafavi S, Kobor MS
Sex-dependent placental methylation quantitative trait loci provide insight into the prenatal origins of childhood onset traits and conditions.
Casazza W, Inkster AM, Del Gobbo GF, Yuan V, Delahaye F, Marsit C, Park YP, Robinson WP, Mostafavi S, Dennis JK
Cell subtype-specific effects of genetic variation in the Alzheimer's disease brain.
Fujita M, Gao Z, Zeng L, McCabe C, White CC, Ng B, Green GS, Rozenblatt-Rosen O, Phillips D, Amir-Zilberstein L, Lee H, Pearse RV, Khan A, Vardarajan BN, Kiryluk K, Ye CJ, Klein HU, Wang G, Regev A, Habib N, Schneider JA, Wang Y, Young-Pearse T, Mostafavi S, Bennett DA, Menon V, De Jager PL
Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.
Mohajeri A, Vaseghi-Shanjani M, Rosenfeld JA, Yang GX, Lu H, Sharma M, Lin S, Salman A, Waqas M, Sababi Azamian M, Worley KC, Del Bel KL, Kozak FK, Rahmanian R, Biggs CM, Hildebrand KJ, Lalani SR, Nicholas SK, Scott DA, Mostafavi S, van Karnebeek C, Henkelman E, Halparin J, Yang CL, Armstrong L, Undiagnosed Diseases Network, Care4Rare Canada Consortium, Turvey SE, Lehman A
AAV5-miHTT-mediated huntingtin lowering improves brain health in a Huntington's disease mouse model.
Thomson SB, Stam A, Brouwers C, Fodale V, Bresciani A, Vermeulen M, Mostafavi S, Petkau TL, Hill A, Yung A, Russell-Schulz B, Kozlowski P, MacKay A, Ma D, Beg MF, Evers MM, Vallès A, Leavitt BR
In silico discovery of small molecules for efficient stem cell differentiation into definitive endoderm.
Novakovsky G, Sasaki S, Fornes O, Omur ME, Huang H, Bayly CL, Zhang D, Lim N, Cherkasov A, Pavlidis P, Mostafavi S, Lynn FC, Wasserman WW
Dynamic networks of psychotic symptoms in adults living in precarious housing or homelessness.
Jones AA, Gicas KM, Mostafavi S, Woodward ML, Leonova O, Vila-Rodriguez F, Procyshyn RM, Cheng A, Buchanan T, Lang DJ, MacEwan GW, Panenka WJ, Barr AM, Thornton AE, Honer WG
Human JAK1 gain of function causes dysregulated myelopoeisis and severe allergic inflammation.
Biggs CM, Cordeiro-Santanach A, Prykhozhij SV, Deveau AP, Lin Y, Del Bel KL, Orben F, Ragotte RJ, Saferali A, Mostafavi S, Dinh L, Dai D, Weinacht KG, Dobbs K, Ott de Bruin L, Sharma M, Tsai K, Priatel JJ, Schreiber RA, Rozmus J, Hosking MC, Shopsowitz KE, McKinnon ML, Vercauteren S, Seear M, Notarangelo LD, Lynn FC, Berman JN, Turvey SE
Mosaic loss of Chromosome Y in aged human microglia.
Vermeulen MC, Pearse R, Young-Pearse T, Mostafavi S
Local Computing Infrastructure for Large Scale Genomic Analysis
Principal investigators: Mostafavi, Sara
Metabolic regulation of immune defenses in newborns
Principal investigators: Lavoie, Pascal
Keywords: Energy Metabolism; Innate Immunity; Monocytes; Ontogeny; Premature Infant; Translation
Analysis of multiomic Data to Accelerate Personalized health interventions against inhaled Toxicants (ADAPT)
Principal investigators: Carlsten, Christopher
Keywords: Air Pollution; Airways; Biosignatures; Crossover; Environment; Lung; Multiomics
Precision Fluid Biomarkers of Traumatic Brain Injury
Principal investigators: Wellington, Cheryl L
Keywords: Biomarkers; Traumatic Brain Injury; Vulnerable Populations
Epigenetic Signatures of Successful Aging
Principal investigators: Kobor, Michael S; Rehkopf, David H
Keywords: Aging; Blood; Centenarians; Demography; Dna Methylation; Epigenetics; Genetic Variation; Health; Longevity
Integrating multiple types of genomics data to identify meaningful associations
Principal investigators: Mostafavi, Sara
Identifying integrative biomarkers of risk and resilience to childhood psychopathology
Principal investigators: Goldenberg, Anna
Keywords: Computational Medicine; Data Integration; Disease Trajectory; Dna Methylation; Machine Learning; Mental Disorders
Automated analysis of big flow cytometry data.
Principal investigators: Brinkman, Ryan
Keywords: Bioinformatics
Prenatal Programming of Children's Mental Health: Epigenetic Mechanisms and Resilience Promotion
Principal investigators: Kobor, Michael S
Keywords: Array Technology; Dna Methylation; Early Life Environments; Environmental Exposures; Epigenetics; Genotyping; Mental Health; Pregnancy; Sex Difference; Social Implications
Training Program in High-Dimensional Bioinformatics (HDB)
Principal investigators: Pavlidis, Paul
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Pediatrics
- Psychiatry
- Biochemistry and Molecular Biology
- MD/PhD Program
- Pathology and Laboratory Medicine
- Terry Fox Laboratory
- Critical Care Medicine
- Other
Co-authors at University of British Columbia, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
Maja Tarailo-Graovac
Biochemistry and Molecular Biology
2 shared papers, latest 2020
Maryam Vaseghi-Shanjani
MD/PhD Program
2 shared papers, latest 2025
Clara van Karnebeek
Pediatrics
2 shared papers, latest 2025
Rudolf Uher
Psychiatry
2 shared papers, latest 2020
Philip Awadalla
Faculty
1 shared papers, latest 2016
Fidel Vila-Rodriguez
Psychiatry
1 shared papers, latest 2022
Stefan Kloiber
Faculty
1 shared papers, latest 2018
Amanda Li
Terry Fox Laboratory
1 shared papers, latest 2020
Piotr Kozlowski
Electrical and Computer Engineering
1 shared papers, latest 2023
Ina Anreiter
Faculty
1 shared papers, latest 2020
Philip Awadalla
Occupational and Environmental Health
1 shared papers, latest 2017
Tony Panzarella
Biostatistics Division
1 shared papers, latest 2017
Ali Bashashati
Pathology and Laboratory Medicine
1 shared papers, latest 2020
Artem Cherkasov
Urologic Sciences
1 shared papers, latest 2023
Michael Gold
Microbiology and Immunology
1 shared papers, latest 2020
Christian Steidl
Experimental Therapeutics
1 shared papers, latest 2020
Gregor Reid
Pediatrics
1 shared papers, latest 2019
Wyeth Wasserman
Medical Genetics
1 shared papers, latest 2020
Brian Cox
Department of Physiology
1 shared papers, latest 2019
Paul Pavlidis
Psychiatry
1 shared papers, latest 2023
Anna Goldenberg
Critical Care Medicine
1 shared papers, latest 2020
Philip Awadalla
Pediatrics/Human Genetics
1 shared papers, latest 2016
Harold Siden
Pediatrics
1 shared papers, latest 2019
Ronan Foley
Oncology
1 shared papers, latest 2017
Michael Kobor
Medical Genetics
1 shared papers, latest 2020
Irwin Ronald Walker
Medicine
1 shared papers, latest 2017
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