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Correction to: Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario.
Published in:
2021
By:
- Lerner-Ellis, Jordan;
- Mighton, Chloe;
- Lazaro, Conxi;
- Watkins, Nicholas;
- Di Gioacchino, Vanessa;
- Wong, Andrew;
- Chang, Martin C.;
- Charames, George S.
Publication type:
Correction Notice
Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario.
Published in:
Journal of Cancer Research & Clinical Oncology, 2021, v. 147, n. 3, p. 871, doi. 10.1007/s00432-020-03377-6
By:
- Lerner-Ellis, Jordan;
- Mighton, Chloe;
- Lazaro, Conxi;
- Watkins, Nicholas;
- Di Gioacchino, Vanessa;
- Wong, Andrew;
- Chang, Martin C.;
- Charames, George S.
Publication type:
Article
Genetic testing for Lynch syndrome in the Province of Ontario.
Published in:
Canadian Journal of Pathology, 2016, v. 8, p. 6
By:
- Wang, Marina;
- Aldubayan, Saud;
- Connor, Ashton A.;
- Wong, Beatrix;
- Mcnamara, Kate;
- Khan, Tahsin;
- Semotiuk, Kara;
- Khalouei, Sam;
- Holter, Spring;
- Aronson, Melyssa;
- Cohen, Zane;
- Gallinger, Steve;
- Charames, George;
- Pollett, Aaron;
- Lerner-Ellis, Jordan
Publication type:
Article
Great expectations: patients' preferences for clinically significant results from genomic sequencing.
Published in:
Human Genetics, 2023, v. 142, n. 4, p. 553, doi. 10.1007/s00439-023-02543-3
By:
- Shickh, Salma;
- Sebastian, Agnes;
- Clausen, Marc;
- Mighton, Chloe;
- Elser, Christine;
- Eisen, Andrea;
- Waldman, Larissa;
- Panchal, Seema;
- Ward, Thomas;
- Carroll, June C.;
- Glogowski, Emily;
- Schrader, Kasmintan A.;
- Lerner-Ellis, Jordan;
- Kim, Raymond H.;
- Thorpe, Kevin E.;
- Bombard, Yvonne;
- the Incidental Genomics Team members to be indexed in PubMed;
- Armel, Susan R.;
- Aronson, Melyssa;
- Baxter, Nancy N.
Publication type:
Article
Patient and public preferences for being recontacted with updated genomic results: a mixed methods study.
Published in:
Human Genetics, 2021, v. 140, n. 12, p. 1695, doi. 10.1007/s00439-021-02366-0
By:
- Mighton, Chloe;
- Clausen, Marc;
- Sebastian, Agnes;
- Muir, Sarah M.;
- Shickh, Salma;
- Baxter, Nancy N.;
- Scheer, Adena;
- Glogowski, Emily;
- Schrader, Kasmintan A.;
- Thorpe, Kevin E.;
- Kim, Theresa H. M.;
- Lerner-Ellis, Jordan;
- Kim, Raymond H.;
- Regier, Dean A.;
- Bayoumi, Ahmed M.;
- Bombard, Yvonne
Publication type:
Article
Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings.
Published in:
Human Genetics, 2021, v. 140, n. 3, p. 493, doi. 10.1007/s00439-020-02220-9
By:
- Reble, Emma;
- Gutierrez Salazar, Mariana;
- Zakoor, Kathleen-Rose;
- Khalouei, Sam;
- Clausen, Marc;
- Kodida, Rita;
- Shickh, Salma;
- Mighton, Chloe;
- Cohn, Iris;
- Schrader, Kasmintan A.;
- Kim, Raymond H.;
- Lerner-Ellis, Jordan;
- Bombard, Yvonne
Publication type:
Article
Rapid Genetic Testing for BRCA1 and BRCA2 Mutations at the Time of Breast Cancer Diagnosis: An Observational Study.
Published in:
Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2021, v. 28, n. 4, p. 2219, doi. 10.1245/s10434-020-09160-8
By:
- Metcalfe, Kelly A.;
- Eisen, Andrea;
- Poll, Aletta;
- Candib, Alexandra;
- McCready, David;
- Cil, Tulin;
- Wright, Frances;
- Lerner-Ellis, Jordan;
- McCuaig, Jeanna;
- Graham, Tracy;
- Sun, Ping;
- Akbari, Mohammad;
- Narod, Steven A.
Publication type:
Article
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers.
Published in:
Nature Genetics, 2015, v. 47, n. 3, p. 257, doi. 10.1038/ng.3202
By:
- Shlien, Adam;
- Meier, Bettina;
- Hong, Ye;
- Gartner, Anton;
- Remke, Marc;
- Thakkar, Neha P;
- Pearson, Christopher E;
- Hodel, Karl P;
- Henninger, Erin E;
- Göksenin, A Yasemin;
- Pursell, Zachary F;
- Bakry, Doua;
- Grant, Ronald;
- Nathan, Paul C;
- Alexander, Sarah;
- Charames, George S;
- Druker, Harriet;
- Lerner-Ellis, Jordan;
- Dvir, Rina;
- Elhasid, Ronit
Publication type:
Article
Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Published in:
2006
By:
- Lerner-Ellis, Jordan P.;
- Tirone, Jamie C.;
- Pawelek, Peter D.;
- Doré, Carole;
- Atkinson, Janet L.;
- Watkins, David;
- Morel, Chantal F.;
- Fujiwara, T. Mary;
- Moras, Emily;
- Hosack, Angela R.;
- Dunbar, Gail V.;
- Antonicka, Hana;
- Forgetta, Vince;
- Dobson, C. Melissa;
- Leclerc, Daniel;
- Gravel, Roy A.;
- Shoubridge, Eric A.;
- Coulton, James W.;
- Lepage, Pierre;
- Rommens, Johanna M.
Publication type:
Correction Notice
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Published in:
Nature Genetics, 2006, v. 38, n. 1, p. 93, doi. 10.1038/ng1683
By:
- Lerner-Ellis, Jordan P;
- Tirone, Jamie C;
- Pawelek, Peter D;
- Doré, Carole;
- Atkinson, Janet L;
- Watkins, David;
- Morel, Chantal F;
- Fujiwara, T Mary;
- Moras, Emily;
- Hosack, Angela R;
- Dunbar, Gail V;
- Antonicka, Hana;
- Forgetta, Vince;
- Dobson, C Melissa;
- Leclerc, Daniel;
- Gravel, Roy A;
- Shoubridge, Eric A;
- Coulton, James W;
- Lepage, Pierre;
- Rommens, Johanna M
Publication type:
Article
Principles of molecular testing for hereditary cancer.
Published in:
Genes, Chromosomes & Cancer, 2022, v. 61, n. 6, p. 356, doi. 10.1002/gcc.23048
By:
- Mighton, Chloe;
- Lerner‐Ellis, Jordan P.
Publication type:
Article
De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities.
Published in:
NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00268-8
By:
- Okur, Volkan;
- Chen, Zefu;
- Vossaert, Liesbeth;
- Peacock, Sandra;
- Rosenfeld, Jill;
- Zhao, Lina;
- Du, Haowei;
- Calamaro, Emily;
- Gerard, Amanda;
- Zhao, Sen;
- Kelsay, Jill;
- Lahr, Ashley;
- Mighton, Chloe;
- Porter, Hillary M.;
- Siemon, Amy;
- Silver, Josh;
- Svihovec, Shayna;
- Fong, Chin-To;
- Grant, Christina L.;
- Lerner-Ellis, Jordan
Publication type:
Article
Tumor BRCA Testing in High Grade Serous Carcinoma: Mutation Rates and Optimal Tissue Requirements.
Published in:
Cancers, 2020, v. 12, n. 11, p. 3468, doi. 10.3390/cancers12113468
By:
- Turashvili, Gulisa;
- Lazaro, Conxi;
- Ying, Shengjie;
- Charames, George;
- Wong, Andrew;
- Hamilton, Krista;
- Yee, Denise;
- Agro, Evangeline;
- Chang, Martin;
- Pollett, Aaron;
- Lerner-Ellis, Jordan
Publication type:
Article
A high frequency of PALB2 mutations in Jamaican patients with breast cancer.
Published in:
Breast Cancer Research & Treatment, 2017, v. 162, n. 3, p. 591, doi. 10.1007/s10549-017-4148-1
By:
- Lerner-Ellis, Jordan;
- Donenberg, Talia;
- Ahmed, Humayun;
- George, Sophia;
- Wharfe, Gilian;
- Chin, Sheray;
- Lowe, Dwight;
- Royer, Robert;
- Zhang, Shiyu;
- Narod, Steven;
- Hurley, Judith;
- Akbari, Mohammad
Publication type:
Article
Phenotypic variability in deficiency of the α subunit of succinate‐CoA ligase.
Published in:
Journal of Inherited Metabolic Disease Reports, 2019, v. 46, n. 1, p. 63, doi. 10.1002/jmd2.12018
By:
- Demirbas, Didem;
- Harris, David J.;
- Arn, Pamela H.;
- Huang, Xiaoping;
- Waisbren, Susan E.;
- Anselm, Irina;
- Lerner‐Ellis, Jordan P.;
- Wong, Lee‐Jun;
- Levy, Harvey L.;
- Berry, Gerard T.
Publication type:
Article
Genetic testing women with newly diagnosed breast cancer: What criteria are the most predictive of a positive test?
Published in:
Cancer Medicine, 2023, v. 12, n. 6, p. 7580, doi. 10.1002/cam4.5515
By:
- Metcalfe, Kelly A.;
- Narod, Steven A.;
- Eisen, Andrea;
- Poll, Aletta;
- Zamani, Neda;
- McCready, David;
- Cil, Tulin D.;
- Wright, Frances C.;
- Lerner‐Ellis, Jordan;
- McCuaig, Jeanna;
- Graham, Tracy;
- Sun, Ping;
- Akbari, Mohammad R.
Publication type:
Article
Canadian COVID-19 host genetics cohort replicates known severity associations.
Published in:
PLoS Genetics, 2024, v. 20, n. 3, p. 1, doi. 10.1371/journal.pgen.1011192
By:
- Garg, Elika;
- Arguello-Pascualli, Paola;
- Vishnyakova, Olga;
- Halevy, Anat R.;
- Yoo, Samantha;
- Brooks, Jennifer D.;
- Bull, Shelley B.;
- Gagnon, France;
- Greenwood, Celia M. T.;
- Hung, Rayjean J.;
- Lawless, Jerald F.;
- Lerner-Ellis, Jordan;
- Dennis, Jessica K.;
- Abraham, Rohan J. S.;
- Garant, Jean-Michel;
- Thiruvahindrapuram, Bhooma;
- Jones, Steven J. M.;
- Strug, Lisa J.;
- Paterson, Andrew D.;
- Sun, Lei
Publication type:
Article
HLA Variation and SARS-CoV-2 Specific Antibody Response.
Published in:
Viruses (1999-4915), 2023, v. 15, n. 4, p. 906, doi. 10.3390/v15040906
By:
- Wolday, Dawit;
- Fung, Chun Yiu Jordan;
- Morgan, Gregory;
- Casalino, Selina;
- Frangione, Erika;
- Taher, Jennifer;
- Lerner-Ellis, Jordan P.
Publication type:
Article
Oestrogen receptor status and survival in women with BRCA2-associated breast cancer.
Published in:
2019
By:
- Metcalfe, Kelly;
- Lynch, Henry T.;
- Foulkes, William D.;
- Tung, Nadine;
- Olopade, Olufunmilayo I.;
- Eisen, Andrea;
- Lerner-Ellis, Jordan;
- Snyder, Carrie;
- Kim, Shana J.;
- Sun, Ping;
- Narod, Steven A.
Publication type:
journal article
The clinical implementation of whole genome sequencing: a conversation with seven scientific experts.
Published in:
Journal of Inherited Metabolic Disease, 2012, v. 35, n. 4, p. 689, doi. 10.1007/s10545-012-9463-4
By:
- Lerner-Ellis, Jordan
Publication type:
Article
Germline whole genome sequencing in adults with multiple primary tumors.
Published in:
Familial Cancer, 2023, v. 22, n. 4, p. 513, doi. 10.1007/s10689-023-00343-2
By:
- Wang, Yiming;
- Ding, Qiliang;
- Prokopec, Stephenie;
- Farncombe, Kirsten M.;
- Bruce, Jeffrey;
- Casalino, Selina;
- McCuaig, Jeanna;
- Szybowska, Marta;
- van Engelen, Kalene;
- Lerner-Ellis, Jordan;
- Pugh, Trevor J.;
- Kim, Raymond H.
Publication type:
Article
Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.
Published in:
Familial Cancer, 2015, v. 14, n. 1, p. 69, doi. 10.1007/s10689-014-9765-9
By:
- Connor, Ashton;
- Katzov-Eckert, Hagit;
- Whelan, Thomas;
- Aronson, Melyssa;
- Lau, Lynette;
- Marshall, Christian;
- Charames, George;
- Pollett, Aaron;
- Gallinger, Steven;
- Lerner-Ellis, Jordan
Publication type:
Article
Genetic testing for Lynch syndrome in the province of Ontario.
Published in:
2016
By:
- Wang, Marina;
- Aldubayan, Saud;
- Connor, Ashton A.;
- Wong, Beatrix;
- Mcnamara, Kate;
- Khan, Tahsin;
- Semotiuk, Kara;
- Khalouei, Sam;
- Holter, Spring;
- Aronson, Melyssa;
- Cohen, Zane;
- Gallinger, Steve;
- Charames, George;
- Pollett, Aaron;
- Lerner‐Ellis, Jordan
Publication type:
journal article
Performance characteristics of screening strategies for Lynch syndrome in unselected women with newly diagnosed endometrial cancer who have undergone universal germline mutation testing.
Published in:
Cancer (0008543X), 2014, v. 120, n. 24, p. 3932, doi. 10.1002/cncr.28933
By:
- Ferguson, Sarah E.;
- Aronson, Melyssa;
- Pollett, Aaron;
- Eiriksson, Lua R.;
- Oza, Amit M.;
- Gallinger, Steven;
- Lerner‐Ellis, Jordan;
- Alvandi, Zahra;
- Bernardini, Marcus Q.;
- MacKay, Helen J.;
- Mojtahedi, Golnessa;
- Tone, Alicia A.;
- Massey, Christine;
- Clarke, Blaise A.
Publication type:
Article
Ethics and genomic medicine, how to navigate decisions in surgical oncology.
Published in:
Journal of Surgical Oncology, 2015, v. 111, n. 1, p. 18, doi. 10.1002/jso.23771
By:
- Devon, Karen M.;
- Lerner-Ellis, Jordan P.;
- Ganai, Sabha;
- Angelos, Peter
Publication type:
Article
Validation of low‐pass genome sequencing for prenatal diagnosis.
Published in:
Prenatal Diagnosis, 2024, v. 44, n. 4, p. 443, doi. 10.1002/pd.6525
By:
- Mighton, Chloe;
- Noor, Abdul;
- Watkins, Nicholas;
- Di Gioacchino, Vanessa;
- Lerner‐Ellis, Jordan;
- Wong, Andrew;
- Mukharryamova, Elvira;
- Anggala, Nina;
- Chitayat, David;
- Greenfeld, Elena
Publication type:
Article
Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
Published in:
Human Mutation, 2009, v. 30, n. 7, p. 1072, doi. 10.1002/humu.21001
By:
- Lerner-Ellis, Jordan P.;
- Anastasio, Natascia;
- Liu, Junhui;
- Coelho, David;
- Suormala, Terttu;
- Stucki, Martin;
- Loewy, Amanda D.;
- Gurd, Scott;
- Grundberg, Elin;
- Morel, Chantal F.;
- Watkins, David;
- Baumgartner, Matthias R.;
- Pastinen, Tomi;
- Rosenblatt, David S.;
- Fowler, Brian
Publication type:
Article
Mutations in the MMAA Gene in Patients With the cblA Disorder of Vitamin B<sub>12</sub> Metabolism.
Published in:
Human Mutation, 2005, v. 25, n. 3, p. 317, doi. 10.1002/humu.20149
By:
- Lerner-Ellis, Jordan P.;
- Dobson, C. Melissa;
- Wai, Timothy;
- Watkins, David;
- Tirone, Jamie C.;
- Leclerc, Daniel;
- Doré, Carole;
- Lepage, Pierre;
- Gravel, Roy A.;
- Rosenblatt, David S.
Publication type:
Article
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B<sub>12</sub> metabolism.
Published in:
Human Mutation, 2004, v. 24, n. 6, p. 509, doi. 10.1002/humu.20104
By:
- Lerner-Ellis, Jordan P.;
- Dobson, C. Melissa;
- Wai, Timothy;
- Watkins, David;
- Tirone, Jamie C.;
- Leclerc, Daniel;
- Doré, Carole;
- Lepage, Pierre;
- Gravel, Roy A.;
- Rosenblatt, David S.
Publication type:
Article
Genome Reporting for Healthy Populations—Pipeline for Genomic Screening from the GENCOV COVID‐19 Study.
Published in:
Current Protocols, 2022, v. 2, n. 10, p. 1, doi. 10.1002/cpz1.534
By:
- Frangione, Erika;
- Chung, Monica;
- Casalino, Selina;
- MacDonald, Georgia;
- Chowdhary, Sunakshi;
- Mighton, Chloe;
- Faghfoury, Hanna;
- Bombard, Yvonne;
- Strug, Lisa;
- Pugh, Trevor;
- Simpson, Jared;
- Hao, Limin;
- Lebo, Matthew;
- Lane, William J.;
- Taher, Jennifer;
- Lerner‐Ellis, Jordan
Publication type:
Article
Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 26, p. 3361, doi. 10.1093/hmg/11.26.3361
By:
- Dobson, C. Melissa;
- Wai, Timothy;
- Leclerc, Daniel;
- Kadir, Hakan;
- Narang, Monica;
- Lerner-Ellis, Jordan P.;
- Hudson, Thomas J.;
- Rosenblatt, David S.;
- Gravel, Roy A.
Publication type:
Article
Maximizing cancer prevention through genetic navigation for Lynch syndrome detection in women with newly diagnosed endometrial and nonserous/nonmucinous epithelial ovarian cancer.
Published in:
Cancer (0008543X), 2021, v. 127, n. 17, p. 3082, doi. 10.1002/cncr.33625
By:
- Kim, Soyoun Rachel;
- Tone, Alicia;
- Kim, Raymond H.;
- Cesari, Matthew;
- Clarke, Blaise A.;
- Eiriksson, Lua;
- Hart, Tae L.;
- Aronson, Melyssa;
- Holter, Spring;
- Lytwyn, Alice;
- Maganti, Manjula;
- Oldfield, Leslie;
- Gallinger, Steven;
- Bernardini, Marcus Q.;
- Oza, Amit M.;
- Djordjevic, Bojana;
- Lerner‐Ellis, Jordan;
- Van de Laar, Emily;
- Vicus, Danielle;
- Pugh, Trevor J.
Publication type:
Article
Performance characteristics of screening strategies to identify Lynch syndrome in women with ovarian cancer.
Published in:
Cancer (0008543X), 2020, v. 126, n. 22, p. 4886, doi. 10.1002/cncr.33144
By:
- Kim, Soyoun Rachel;
- Tone, Alicia;
- Kim, Raymond H.;
- Cesari, Matthew;
- Clarke, Blaise A.;
- Eiriksson, Lua;
- Hart, Tae;
- Aronson, Melyssa;
- Holter, Spring;
- Lytwyn, Alice;
- Maganti, Manjula;
- Oldfield, Leslie;
- Gallinger, Steven;
- Bernardini, Marcus Q.;
- Oza, Amit M.;
- Djordjevic, Bojana;
- Lerner‐Ellis, Jordan;
- Van de Laar, Emily;
- Vicus, Danielle;
- Pugh, Trevor J.
Publication type:
Article

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