Faculty profile

Yiming Wang

ResearcherPediatrics/Human GeneticsUniversity of Toronto

This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Toronto directory, so their courses and email address may be missing. Find their university profile.

Yiming Wang

Researcher

Pediatrics/Human Genetics

Health Sciences

University of Toronto

Toronto, Ontario, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
11 publications in the last five years, latest in 2026.
Senior (last) author on 2 recent papers, a sign of leading a research group.
Principal investigator on 1 research grant (1 CIHR), most recently in 2024.

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

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Publications

Citations

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Collaborators

Grants

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

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Signals and details

Research

Copy Number Variants (Cnv)Noninvasive Prenatal Diagnosis Placental Methylome

Latest papers

Future Trends in Cancer Prevention and Interception in Cancer Predisposition Syndromes: Leveraging Insights From High-Risk Populations.
International journal of cancer · 2026 · first author
Bridging the Diagnostic Gap in Neurofibromatosis Type 1: When to Consider NF1 cDNA Sequencing.
Pediatric dermatology · 2026 · senior author
Multigenerational Huriez syndrome with marked intrafamilial heterogeneity and cutaneous squamous cell carcinoma burden.
Clinical and experimental dermatology · 2026

All 29 publications

Latest funding

Mapping variant effects and genetic modifiers for NF1
CIHR · 2026 · Co-investigator
$1,174,276
Development of a novel approach for noninvasive prenatal CNV detection by establishing the human placental methylome in early pregnancy
CIHR · 2024 · Nominated PI
$300,000

All 2 grants and awards

29 publications.

Future Trends in Cancer Prevention and Interception in Cancer Predisposition Syndromes: Leveraging Insights From High-Risk Populations.

Wang Y, Malkin D, Lipkin SM

International journal of cancer2026First author

DOI: 10.1002/ijc.70674 PMID: 42538617

Bridging the Diagnostic Gap in Neurofibromatosis Type 1: When to Consider NF1 cDNA Sequencing.

Doolan BJ, Chiramel MJ, Hendry M, Shugar A, Chen Y, Lara-Corrales I, Wang Y

Pediatric dermatology2026Senior author

DOI: 10.1111/pde.70257 PMID: 42125802

Multigenerational Huriez syndrome with marked intrafamilial heterogeneity and cutaneous squamous cell carcinoma burden.

Doolan BJ, Wang Y, Lara-Corrales I, Lee M, Shugar A, Pope E

Clinical and experimental dermatology2026

DOI: 10.1093/ced/llag413 PMID: 42786959

Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti.

Pipko N, Oh RY, Kaplan A, Shugar A, Szuto A, Weinstein M, Yoon G, Mendoza-Londono R, Pope E, Young T, Marshall CR, Costain G, Lara-Corrales I, Wang Y

The British journal of dermatology2025Senior author

DOI: 10.1093/bjd/ljae462 PMID: 39579378

Salvianolic acid B inhibits thrombosis and directly blocks the thrombin catalytic site.

Neves MAD, Ni TT, Mackeigan DT, Shoara AA, Lei X, Slavkovic S, Yu SY, Stratton TW, Gallant RC, Zhang D, Xu XR, Fernandes C, Zhu G, Hu X, Chazot N, Donaldson LW, Johnson PE, Connelly K, Rand M, Wang Y, Ni H

Research and practice in thrombosis and haemostasis2024

DOI: 10.1016/j.rpth.2024.102443 PMID: 38993621

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

Blayney GV, Laffan E, Jacob PA, Baptiste CD, Gabriel H, Sparks TN, Yaron Y, Norton ME, Diderich K, Wang Y, Chong K, Chitayat D, Saini N, Aggarwal S, Pauta M, Borrell A, Gilmore K, Chandler NJ, Allen S, Vora N, Noor A, Monaghan C, Kilby MD, Wapner RJ, Chitty LS, Mone F

Prenatal diagnosis2024

DOI: 10.1002/pd.6466 PMID: 38054560

Germline whole genome sequencing in adults with multiple primary tumors.

Wang Y, Ding Q, Prokopec S, Farncombe KM, Bruce J, Casalino S, McCuaig J, Szybowska M, van Engelen K, Lerner-Ellis J, Pugh TJ, Kim RH

Familial cancer2023First author

DOI: 10.1007/s10689-023-00343-2 PMID: 37481477

Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report.

Wang Y, Lazier J, Myles-Reid D, Noor A, Chitayat D, Greenfeld E

Clinical case reports2023First author

DOI: 10.1002/ccr3.6632 PMID: 37102101

Career development of international medical graduates in Canada: status of the unmatched.

Wang Y, Das RLV, Lapa T, Marosan P, Pawliuk R, Chable HD, Lake D, Lofters A

Humanities & social sciences communications2023First author

DOI: 10.1057/s41599-023-01534-z PMID: 36741982

c-Mpl-del, a c-Mpl alternative splicing isoform, promotes AMKL progression and chemoresistance.

Li F, Xiong Y, Yang M, Chen P, Zhang J, Wang Q, Xu M, Wang Y, He Z, Zhao X, Huang J, Gu X, Zhang L, Sun R, Sun X, Li J, Ou J, Xu T, Huang X, Cao Y, Xu XR, Karakas D, Li J, Ni H, Zhang Q

Cell death & disease2022

DOI: 10.1038/s41419-022-05315-5 PMID: 36229456

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Yiming Wang

Research

Latest papers

Latest funding

Future Trends in Cancer Prevention and Interception in Cancer Predisposition Syndromes: Leveraging Insights From High-Risk Populations.

Bridging the Diagnostic Gap in Neurofibromatosis Type 1: When to Consider NF1 cDNA Sequencing.

Multigenerational Huriez syndrome with marked intrafamilial heterogeneity and cutaneous squamous cell carcinoma burden.

Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti.

Salvianolic acid B inhibits thrombosis and directly blocks the thrombin catalytic site.

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

Germline whole genome sequencing in adults with multiple primary tumors.

Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report.

Career development of international medical graduates in Canada: status of the unmatched.

c-Mpl-del, a c-Mpl alternative splicing isoform, promotes AMKL progression and chemoresistance.

Mapping variant effects and genetic modifiers for NF1

Development of a novel approach for noninvasive prenatal CNV detection by establishing the human placental methylome in early pregnancy

Frequent collaborators

Heyu Ni

Slava Epelman

Abdul Noor

David Chitayat

Mansoor Husain

Seema Mital

Filio Billia

David Malkin

Myron Cybulsky

Jordan Lerner-Ellis

Kim Connelly

Khosrow Adeli

Aisha Lofters

Aisha Lofters

Gregory Costain

Catherine Pauline Ma Hayward

Deidre Lake

William Sheffield

Peter Lawrence Gross

David Lillicrap

Yiming Wang

Research

Latest papers

Latest funding

Future Trends in Cancer Prevention and Interception in Cancer Predisposition Syndromes: Leveraging Insights From High-Risk Populations.

Bridging the Diagnostic Gap in Neurofibromatosis Type 1: When to Consider NF1 cDNA Sequencing.

Multigenerational Huriez syndrome with marked intrafamilial heterogeneity and cutaneous squamous cell carcinoma burden.

Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti.

Salvianolic acid B inhibits thrombosis and directly blocks the thrombin catalytic site.

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

Germline whole genome sequencing in adults with multiple primary tumors.

Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A&#xa0;case&#xa0;report.

Career development of international medical graduates in Canada: status of the unmatched.

c-Mpl-del, a c-Mpl alternative splicing isoform, promotes AMKL progression and chemoresistance.

Mapping variant effects and genetic modifiers for NF1

Development of a novel approach for noninvasive prenatal CNV detection by establishing the human placental methylome in early pregnancy

Frequent collaborators

Heyu Ni

Slava Epelman

Abdul Noor

David Chitayat

Mansoor Husain

Seema Mital

Filio Billia

David Malkin

Myron Cybulsky

Jordan Lerner-Ellis

Kim Connelly

Khosrow Adeli

Aisha Lofters

Aisha Lofters

Gregory Costain

Catherine Pauline Ma Hayward

Deidre Lake

William Sheffield

Peter Lawrence Gross

David Lillicrap

Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report.