Faculty profile

Olga Jarinova

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Assistant ProfessorPathology and Laboratory MedicineUniversity of Ottawa

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Research

Read how they describe their research on their University of Ottawa profile.

Latest papers

Understanding the decision of parents to opt‐out of medically actionable secondary findings offered through genome sequencing
Journal of Genetic Counseling · 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
BMJ Open · 2026
Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing Program
Canadian Journal of Neurological Sciences · 2026

All 32 publications

32 publications.

Understanding the decision of parents to opt‐out of medically actionable secondary findings offered through genome sequencing

Hansen A, Luca S, Moran O, Babul‐Hirji R, Coe TB, Wilk K, Assamad D, Fooks K, Venkataramanan V, Shickh S

Journal of Genetic Counseling2026

DOI: 10.1002/jgc4.70218

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study

Assamad D, Hansen A, Fooks K, Luca S, Venkataramanan V, Hsue E, Shickh S, Yan J, Wu V, Badalato L

BMJ Open2026

DOI: 10.1136/bmjopen-2025-115821

Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing Program

Balci TB, Schenkel LC, Rastin C, Jones K, Lomax LB, Turowec J, Kerkhof J, Bhai P, Jarinova O, Hewson S

Canadian Journal of Neurological Sciences2026

DOI: 10.1017/cjn.2025.69

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.

Hespe S, Singer ES, Reuter C, Murray B, Jordan E, Chowns J, Peters S, Mayers M, Gray B, Hershberger RE, Owens AT, Semsarian C, Waddell A, Asatryan B, Owens E, Thaxton C, Adduru ML, Anderson K, Brown EE, Hoffman-Andrews L, Stafford F, Bagnall RD, Bronicki L, Callewaert B, Chahal CAA, James CA, Jarinova O, Landstrom AP, McNally EM, Muiño-Mosquera L, Parikh V, Walsh R, Wayburn B, Ware JS, Parker BL, Porrello ER, Elliott DA, McNamara JW, Ingles J

Circulation. Genomic and precision medicine2025

DOI: 10.1161/circgen.124.004976 PMID: 40255155

Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel.

Hespe S, Waddell A, Asatryan B, Owens E, Thaxton C, Adduru ML, Anderson K, Brown EE, Hoffman-Andrews L, Jordan E, Josephs K, Mayers M, Peters S, Stafford F, Bagnall RD, Bronicki L, Callewaert B, Chahal CAA, James CA, Jarinova O, Landstrom AP, McNally EM, Murray B, Muiño-Mosquera L, Parikh V, Reuter C, Walsh R, Wayburn B, Ware JS, Ingles J

Journal of the American College of Cardiology2025

DOI: 10.1016/j.jacc.2024.12.010 PMID: 39971408

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy.

medRxiv : the preprint server for health sciences2024

DOI: 10.1101/2024.07.29.24311195 PMID: 39132495

Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.

Ungar WJ, Hayeems RZ, Marshall CR, Gillespie MK, Szuto A, Chisholm C, James Stavropoulos D, Huang L, Jarinova O, Wu V, Tsiplova K, Lau L, Lee W, Venkataramanan V, Sawyer S, Mendoza-Londono R, Somerville MJ, Boycott KM, Genome Sequencing Ontario Secondary Findings Study Team

Clinical therapeutics2023

DOI: 10.1016/j.clinthera.2023.06.004 PMID: 37453830

Fetal akinesia deformation sequence syndrome associated with recessive TTN variants.

Alkhunaizi E, Martin N, Jelin AC, Rosner M, Bailey DJ, Steiner LA, Lakhani S, Ji W, Katzman PJ, Forster KR, Jarinova O, Shannon P, Chitayat D, Care4Rare Canada Consortium

American journal of medical genetics. Part A2023

DOI: 10.1002/ajmg.a.63071 PMID: 36495114

Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy.

Smith IC, Pileggi CA, Wang Y, Kernohan K, Hartley T, McMillan HJ, Sampaio ML, Melkus G, Woulfe J, Parmar G, Bourque PR, Breiner A, Zwicker J, Pringle CE, Jarinova O, Lochmüller H, Dyment DA, Brais B, Boycott KM, Care4Rare Canada Consortium,, Hekimi S, Harper ME, Warman-Chardon J

Neurology. Genetics2023

DOI: 10.1212/nxg.0000000000200048 PMID: 37077559

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Josephs KS, Roberts AM, Theotokis P, Walsh R, Ostrowski PJ, Edwards M, Fleming A, Thaxton C, Roberts JD, Care M

Genome Medicine202337 citationsOpen Access

DOI: 10.1186/s13073-023-01246-8 PMID: W4387874656

Profile data last refreshed on September 25, 2026 from the university directory, publication records and CIHR, NSERC and SSHRC funding.

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Olga Jarinova

Research

Latest papers

Understanding the decision of parents to opt‐out of medically actionable secondary findings offered through genome sequencing

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study

Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing Program

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.

Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel.

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy.

Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.

Fetal akinesia deformation sequence syndrome associated with recessive TTN variants.

Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy.

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Frequent collaborators

Lucas Bronicki

Jean McGowan-Jordan

Taila Hartley

Pavel Geier

Mark Tarnopolsky

Jason Roberts

Mary-Ellen Harper

Marc Ekker

Jacek Majewski

Michael Gollob

Rafik Tadros

Lauren Chad

Bekim Sadikovic

Jana Feberova

Karine Khatchadourian

Nadya Ben Fadel

Mélanie Beaulieu Bergeron

Bernard Brais

Dennis Bulman

Bernard Brais

John Woulfe

Olga Jarinova

Research

Latest papers

Understanding the decision of parents to opt‐out of medically actionable secondary findings offered through genome sequencing

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study

Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing Program

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy.

Genes Associated With Hypertrophic&#xa0;Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel.

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy.

Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.

Fetal akinesia deformation sequence syndrome associated with recessive TTN variants.

Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor Neuropathy.

Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

Frequent collaborators

Lucas Bronicki

Jean McGowan-Jordan

Taila Hartley

Pavel Geier

Mark Tarnopolsky

Jason Roberts

Mary-Ellen Harper

Marc Ekker

Jacek Majewski

Michael Gollob

Rafik Tadros

Lauren Chad

Bekim Sadikovic

Jana Feberova

Karine Khatchadourian

Nadya Ben Fadel

Mélanie Beaulieu Bergeron

Bernard Brais

Dennis Bulman

Bernard Brais

John Woulfe

Genes Associated With Hypertrophic Cardiomyopathy: A Reappraisal by the ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel.