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Elena Greenfeld

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Associate ProfessorDepartment of Laboratory Medicine & PathobiologyUniversity of Toronto

Elena Greenfeld

Associate Professor

Department of Laboratory Medicine & Pathobiology

Temerty Faculty of Medicine

University of Toronto

Toronto, Ontario, Canada

Supervision signals

Professors usually supervise graduate students in their department's programs.
12 publications in the last five years, latest in 2026.
Senior (last) author on 3 recent papers, a sign of leading a research group.

These signals come from public records, including federal and provincial funding decisions. Ask the professor or the graduate program whether they are taking new students.

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Publications

Citations

Collaborators

Publications by year

Counts cover the publications linked to this profile. Citations and the h-index appear when the source records them.

Roles and appointments

Co-Head of the Division of Diagnostic Medical Genetics

Profiles and links

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Signals and details

Research

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

Latest papers

Transforming blood-derived episignatures into cell-type-agnostic classifiers: A shortcut to prenatal episignatures
American Journal of Human Genetics · 2026
Findings from comprehensive genome sequencing in the Canadian population: Results from the GENCOV Study
Genetics in Medicine Open · 2026
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens
Genetics in Medicine · 2026

All 12 publications

12 publications.

Transforming blood-derived episignatures into cell-type-agnostic classifiers: A shortcut to prenatal episignatures

Reko N, Torabi-Marashi A, Kallurkar P, Goodman SJ, Awamleh Z, Turinsky AL, Grafodatskaya D, Russell BE, Chong K, Ko JM

American Journal of Human Genetics2026Open Access

DOI: 10.1016/j.ajhg.2026.06.017

Findings from comprehensive genome sequencing in the Canadian population: Results from the GENCOV Study

Casalino S, Aujla N, Frangione E, Mahajan R, Di Iorio D, Fung CYJ, Jayachandran L, MacDonald G, Morgan G, Wolday D

Genetics in Medicine Open2026Open Access

DOI: 10.1016/j.gimo.2026.104372

Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens

Mighton C, Reble E, Sam J, Kodida R, Shickh S, Clausen M, Hirjikaka D, Grewal S, Panchal S, Piccinin C

Genetics in Medicine2026Open Access

DOI: 10.1016/j.gim.2025.101599

A digital microfluidic platform for cell-based non-invasive testing.

Siriwardena D, Dryden MDM, Chamberlain MD, Taylor C, Dupoiron L, Gulati S, Abbas F, Lamanna J, Chitayat D, Wheeler AR, Greenfeld E

iScience2026Senior authorOpen Access

DOI: 10.1016/j.isci.2026.116413 PMID: 42375540

The spectrum of copy number variation in the Pan-Canadian HostSeq databank.

Aujla N, Thiruvahindrapuram B, Casalino S, Frangione E, Mahajan R, Di Iorio D, Fung CYJ, Jayachandran L, MacDonald G, Morgan G, Wolday D, Young J, Arshad M, Clausen M, Arnoldo S, Binnie A, Borgundvaag B, Chowdhary S, Dagher M, Devine L, Friedman SM, Gingras AC, Goneau LW, Khan Z, Lapadula E, Mazzulli T, McGeer A, McLeod S, Mighton C, Pugh TJ, Richardson D, Simpson J, Stern S, Taher A, Strug L, Bombard Y, Faghfoury H, Greenfeld E, CGEn HostSeq Initiative, Scherer SW, Taher J, Noor A, Lerner-Ellis J

PloS one2026

DOI: 10.1371/journal.pone.0359210 PMID: 42789588

Opportunistic genomic screening has clinical utility: An interventional cohort study

Mighton C, Kodida R, Shickh S, Clausen M, Reble E, Sam J, Grewal S, Hirjikaka D, Panchal S, Piccinin C

Genetics in Medicine202510 citationsOpen Access

DOI: 10.1016/j.gim.2024.101323

Validation of low-pass genome sequencing for prenatal diagnosis.

Mighton C, Noor A, Watkins N, Di Gioacchino V, Lerner-Ellis J, Wong A, Mukharryamova E, Anggala N, Chitayat D, Greenfeld E

Prenatal diagnosis20247 citationsSenior authorOpen Access

DOI: 10.1002/pd.6525 PMID: 38279846

A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention Study.

Casalino S, Mighton C, Clausen M, Frangione E, Aujla N, MacDonald G, Young J, Fung CYJ, Morgan G, Arnoldo S, Bearss E, Binnie A, Borgundvaag B, Chowdhary S, Dagher M, Devine L, Friedman SM, Hao L, Khan Z, Lane W, Lapadula E, Lebo M, Richardson D, Stern S, Strug L, Taher A, Greenfeld E, Noor A, Faghfoury H, Taher J, Bombard Y, Lerner-Ellis J, GENCOV Study Workgroup

Genetics in medicine : official journal of the American College of Medical Genetics20246 citationsOpen Access

DOI: 10.1016/j.gim.2024.101272 PMID: 39301805

Revisiting the Implications of a Wide or Narrow Fetal Cavum Septi Pellucidi.

Sichitiu J, Ghannad-Zadeh K, Van Mieghem T, Toi A, Greenfeld E, Chitayat D, Shinar S

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine2024

DOI: 10.1002/jum.16470 PMID: 38708946

Genome screening, reporting, and genetic counseling for healthy populations.

Casalino S, Frangione E, Chung M, MacDonald G, Chowdhary S, Mighton C, Faghfoury H, Bombard Y, Strug L, Pugh TJ, Simpson J, Arnoldo S, Aujla N, Bearss E, Binnie A, Borgundvaag B, Chertkow H, Clausen M, Dagher M, Devine L, Di Iorio D, Friedman SM, Fung CYJ, Gingras AC, Goneau LW, Kaushik D, Khan Z, Lapadula E, Lu T, Mazzulli T, McGeer A, McLeod SL, Morgan G, Richardson D, Singh H, Stern S, Taher A, Wong I, Zarei N, Greenfeld E, Hao L, Lebo M, Lane W, Noor A, Taher J, Lerner-Ellis J

Human genetics202312 citationsOpen Access

DOI: 10.1007/s00439-022-02480-7 PMID: 36331656

Profile data last refreshed on September 29, 2026 from the university directory, publication records and public research funding records.

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Elena Greenfeld

Research

Latest papers

Transforming blood-derived episignatures into cell-type-agnostic classifiers: A shortcut to prenatal episignatures

Findings from comprehensive genome sequencing in the Canadian population: Results from the GENCOV Study

Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens

A digital microfluidic platform for cell-based non-invasive testing.

The spectrum of copy number variation in the Pan-Canadian HostSeq databank.

Opportunistic genomic screening has clinical utility: An interventional cohort study

Validation of low-pass genome sequencing for prenatal diagnosis.

A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention Study.

Revisiting the Implications of a Wide or Narrow Fetal Cavum Septi Pellucidi.

Genome screening, reporting, and genetic counseling for healthy populations.

Frequent collaborators

Abdul Noor

Jordan Lerner-Ellis

David Chitayat

Yvonne Bombard

Luke Devine

Ahmed Taher

Saranya Arnoldo

Alexandra Binnie

Jennifer Taher

Hanna Faghfoury

Tony Mazzulli

Allison McGeer

Anne-Claude Gingras

Raymond Kim

Kelvin Chan

Kasmintan Schrader

Lisa Strug

Trevor Pugh

Kevin Thorpe

Andrea Eisen

Yiming Wang

Shelley McLeod

Ants Toi

Tim Van Mieghem

Shiri Shinar

Patrick Shannon

Ebba Alkhunaizi

Christian Marshall

Christine Elser

Aaron Wheeler

Dawit Wolday