Leanne de Kock

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 13

Top Venues

Nature communications

Acta neuropathologica

Journal of medical genetics

Genes, chromosomes & cancer

McGill University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

McGill University

Canada

PHD :: Department of Human Genetics

Publications

Elena Denisenko, Leanne de Kock, Adeline Tan, Aaron B Beasley, Maria Beilin, Matthew E Jones, Rui Hou, Dáithí Ó Muirí, Sanela Bilic, G Raj K A Mohan, Stuart Salfinger, Simon A Fox, Khaing P W Hmon, Jiansha Wu, Youngmi Kim, Rhea John, Tami S Gilderman, Emily E Killingbeck, Elin Solomonovna Gray, Paul Andrew Cohen, Yu Yu, Alistair R R Forrest
Spatial transcriptomics reveals discrete tumour microenvironments and autocrine loops within ovarian cancer subclones. Nature communications 15 (1) (2024)
Elena Denisenko, Leanne de Kock, Adeline Tan, Aaron B Beasley, Maria Beilin, Matthew E Jones, Rui Hou, Dáithí Ó Muirí, Sanela Bilic, G Raj K A Mohan, Stuart Salfinger, Simon A Fox, Khaing P W Hmon, Jiansha Wu, Youngmi Kim, Rhea John, Tami S Gilderman, Emily E Killingbeck, Elin Solomonovna Gray, Paul Andrew Cohen, Yu Yu, Alistair R R Forrest
Spatial transcriptomics reveals discrete tumour microenvironments and autocrine loops within ovarian cancer subclones. Nature communications 15 (1) (2024)
Elena Denisenko, Leanne de Kock, Adeline Tan, Aaron B Beasley, Maria Beilin, Matthew E Jones, Rui Hou, Dáithí Ó Muirí, Sanela Bilic, G Raj K A Mohan, Stuart Salfinger, Simon A Fox, Khaing P W Hmon, Jiansha Wu, Youngmi Kim, Rhea John, Tami S Gilderman, Emily E Killingbeck, Elin Solomonovna Gray, Paul Andrew Cohen, Yu Yu, Alistair R R Forrest
Spatial transcriptomics reveals discrete tumour microenvironments and autocrine loops within ovarian cancer subclones. Nature communications 15 (1) (2024)
Leanne de Kock, Alexanne Cuillerier, Meredith Gillespie, Madeline Couse, Taila Hartley, Wendy Mears, Francois P Bernier, Albert E Chudley, Patrick Frosk, Sarah M Nikkel, A Micheil Innes, Julie Lauzon, Maryann Thomas, Andrea Guerin, Christine M Armour, Rosanna Weksberg, James N Scott, Debra Watkins, Shirley Harvey, Cheryl Cytrynbaum, null null, Kristin D Kernohan, Kym M Boycott
Molecular characterization of 13 patients with PIK3CA-related overgrowth spectrum using a targeted deep sequencing approach. American journal of medical genetics. Part A (2023)
Taila Hartley, Élisabeth Soubry, Meryl Acker, Matthew Osmond, Madeline Couse, Meredith K Gillespie, Yoko Ito, Aren E Marshall, Gabrielle Lemire, Lijia Huang, Caitlin Chisholm, Alison J Eaton, E Magda Price, James E Dowling, Arun K Ramani, Roberto Mendoza-Londono, Gregory Costain, Michelle M Axford, Anna Szuto, Vanda McNiven, Nadirah Damseh, Rebekah Jobling, Leanne de Kock, Bahareh A Mojarad, Ted Young, Zhuo Shao, Robin Z Hayeems, Ian D Graham, Mark A Tarnopolsky, Lauren Brady, Christine M Armour, Michael Geraghty, Julie Richer, Sarah Sawyer, Matthew Lines, Saadet Mercimek-Mahmutoglu, Melissa T Carter, Gail Graham, Peter Kannu, Joanna Lazier, Chumei Li, Ritu B Aul, Tugce B Balci, Nomazulu Dlamini, Lauren Badalato, Andrea Guerin, Jagdeep Walia, David Chitayat, Ronald Cohn, Hanna Faghfoury, Cynthia Forster-Gibson, Hernan Gonorazky, Eyal Grunebaum, Michal Inbar-Feigenberg, Natalya Karp, Chantal Morel, Alison Rusnak, Neal Sondheimer, Jodi Warman-Chardon, Priya T Bhola, Danielle K Bourque, Inara Chacon Fonseca, Lauren Chad, Pranesh Chakraborty, Karen Chong, Asif Doja, Elaine Suk-Ying Goh, Maha Saleh, null null, Beth K Potter, Christian R Marshall, David A Dyment, Kristin Kernohan, Kym M Boycott
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data. Clinical genetics (2022)
Anne-Sophie Chong, María Apellániz-Ruiz, Leanne de Kock, Dorothée Bouron-Dal Soglio, William R Doyle, John R Priest, Barbara Rivera, William D Foulkes
Likely foregut endoderm origin for a postzygotic mutation affecting the RNase IIIb domain of DICER1. Journal of medical genetics (2021)
Javad Nadaf, Leanne de Kock, Anne-Sophie Chong, Marta Korbonits, Paul Thorner, Naciba Benlimame, Lili Fu, Andrew Peet, Justin Warner, Oswald Ploner, Shanop Shuangshoti, Steffen Albrecht, Nancy Hamel, John R Priest, Barbara Rivera, Jiannis Ragoussis, William D Foulkes
Molecular characterization of DICER1-mutated pituitary blastoma. Acta neuropathologica 141 (6) (2021)
Emeli Pontén, Sofia Frisk, Fulya Taylan, Raquel Vaz, Sandra Wessman, Leanne de Kock, Niklas Pal, William D Foulkes, Kristina Lagerstedt-Robinson, Ann Nordgren
A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1. Journal of medical genetics (2020)
Leanne de Kock, Mona K Wu, William D Foulkes
Ten years of DICER1 mutations: Provenance, distribution, and associated phenotypes. Human mutation 40 (11) (2019)
Leanne de Kock, Morten Hillmer, Rabea Wagener, Dorothée Bouron-Dal Soglio, Nelly Sabbaghian, Reiner Siebert, John R Priest, Michal Miller, William D Foulkes
Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome. Genes, chromosomes & cancer 58 (8) (2019)
Leanne de Kock, John R Priest, William D Foulkes, Sanda Alexandrescu
An update on the central nervous system manifestations of DICER1 syndrome. Acta neuropathologica 139 (4) (2019)
Leanne de Kock, Dominique Geoffrion, Barbara Rivera, Rabea Wagener, Nelly Sabbaghian, Susanne Bens, Benjamin Ellezam, Dorothée Bouron-Dal Soglio, Jessica Ordóñez, Stephanie Sacharow, Jose Fernando Polo Nieto, R Paul Guillerman, Gordan M Vujanic, John R Priest, Reiner Siebert, William D Foulkes
Multiple DICER1-related tumors in a child with a large interstitial 14q32 deletion. Genes, chromosomes & cancer 57 (5) (2018)
Leanne de Kock, Somayyeh Fahiminiya, Pierre O Fiset, Itziar Astigarraga, Van-Hung Nguyen, Steffen Albrecht, William D Foulkes
Infantile Pulmonary Teratoid Tumor. The New England journal of medicine 378 (23) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Leanne de Kock