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Wendy Meschino

Research Profile

Physiology

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Genetic Counseling

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Tianhua Huang; Nathalie Lepage; Wendy S Meschino; Nan Okun; Shamim Rashid; Ritu Aul; Alan Dennis; Barry Hoffman; Sandra A Farrell
The impact of maternal weight discrepancies on prenatal screening results for Down syndrome.
Mary Jane Esplen; Jon Hunter; Kara Semotiuk; Brenda Wilson; Jiahui Wong; Judith Allanson; Melyssa Aronson; Louise Bordeleau; Joan L Bottorff; Mario Cappelli; June Carroll; Nicole Charlemagne; Michel Dorval; Wendy S Meschino
Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study.
June C Carroll; Mary Jane Esplen; Sandra Farrell; Gail E Graham; Jennifer MacKenzie; Wendy S Meschino; Preeti Prakash; Andrea Rideout; Cheryl Shuman; Sherry Taylor; Judith Allanson; Sean Blaine; Brenda J Wilson; Stasey Tobin
Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changes.

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2013: Tianhua Huang; Nathalie Lepage; Wendy S Meschino; Nan Okun; Shamim Rashid; Ritu Aul; Alan Dennis; Barry Hoffman; Sandra A Farrell
The impact of maternal weight discrepancies on prenatal screening results for Down syndrome.
Prenatal diagnosis 2013;33(5):471-6.
2013: Mary Jane Esplen; Jon Hunter; Kara Semotiuk; Brenda Wilson; Jiahui Wong; Judith Allanson; Melyssa Aronson; Louise Bordeleau; Joan L Bottorff; Mario Cappelli; June Carroll; Nicole Charlemagne; Michel Dorval; Wendy S Meschino
Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study.
BMJ open 2013;3(3):.
2013: June C Carroll; Mary Jane Esplen; Sandra Farrell; Gail E Graham; Jennifer MacKenzie; Wendy S Meschino; Preeti Prakash; Andrea Rideout; Cheryl Shuman; Sherry Taylor; Judith Allanson; Sean Blaine; Brenda J Wilson; Stasey Tobin
Maternal age-based prenatal screening for chromosomal disorders: attitudes of women and health care providers toward changes.
Canadian family physician Médecin de famille canadien 2013;59(1):e39-47.
2011: June C Carroll; Judith Allanson; Sean M Blaine; Jeremy Grimshaw; Wendy S Meschino; Joanne A Permaul; Brenda J Wilson; Ian D Graham
GenetiKit: a randomized controlled trial to enhance delivery of genetics services by family physicians.
Family practice 2011;28(6):615-23.
2010: Kenneth T E Chang; Glenn P Taylor; Wendy S Meschino; Paul F Kantor; Ernest Cutz
Mitogenic cardiomyopathy: a lethal neonatal familial dilated cardiomyopathy characterized by myocyte hyperplasia and proliferation.
Human pathology 2010;41(7):1002-8.
2010: Carol Cremin; June C Carroll; Judith Allanson; Sean M Blaine; Heather Dorman; Clare A Gibbons; Christina Honeywell; Wendy S Meschino; Joanne Permaul; Brenda J Wilson
Genetics: factor V Leiden.
Canadian family physician Médecin de famille canadien 2010;56(4):353.
2010: Clare A Gibbons; Judith Allanson; Sean M Blaine; Carol Cremin; Heather Dorman; Christina Honeywell; Wendy S Meschino; Joanne Permaul; June C Carroll
Genetics: Preimplantation genetic diagnosis.
Canadian family physician Médecin de famille canadien 2010;56(3):247.
2010: Carol Cremin; Sean M Blaine; Judith Allanson; Heather Dorman; Clare A Gibbons; Christina Honeywell; Wendy S Meschino; Joanne Permaul; June C Carroll
Genetics: familial melanoma.
Canadian family physician Médecin de famille canadien 2010;56(1):31.
2009: Andrea L Rideout; June C Carroll; Sean M Blaine; Carol Cremin; Heather Dorman; Clare A Gibbons; Christina Honeywell; Wendy S Meschino; Joanne Permaul; Judith Allanson
Genetics: schizophrenia.
Canadian family physician Médecin de famille canadien 2009;55(12):1207.
2009: June C Carroll; Andrea L Rideout; Brenda J Wilson; Judith Md Allanson; Sean M Blaine; Mary Jane Esplen; Sandra A Farrell; Gail E Graham; Jennifer MacKenzie; Wendy S Meschino; Fiona Miller; Preeti Prakash; Cheryl Shuman; Anne Summers; Sherry Taylor
Genetic education for primary care providers: improving attitudes, knowledge, and confidence.
Canadian family physician Médecin de famille canadien 2009;55(12):e92-9.
2009: Christina Honeywell; Wendy S Meschino; Judith Allanson; Sean M Blaine; Carol Cremin; Heather Dorman; Clare A Gibbons; Joanne Permaul; June C Carroll
Genetics: Hypertrophic cardiomyopathy.
Canadian family physician Médecin de famille canadien 2009;55(11):1095.
2009: Wendy S Meschino; Clare A Gibbons; Judith Allanson; Sean M Blaine; Carol Cremin; Heather Dorman; Christina Honeywell; Joanne Permaul; Brenda J Wilson; June C Carroll
Genetics: Newborn screening for sickle cell anemia.
Canadian family physician Médecin de famille canadien 2009;55(10):1001.
2009: Heather Dorman; Wendy S Meschino; Judith Allanson; Sean M Blaine; Carol Cremin; Clare A Gibbons; Christina Honeywell; Joanne Permaul; June C Carroll
Genetics: type 2 diabetes.
Canadian family physician Médecin de famille canadien 2009;55(9):893.
2009: Sean M Blaine; Christina Honeywell; Judith Allanson; Carol Cremin; Heather Dorman; Clare A Gibbons; Wendy S Meschino; Joanne Permaul; June C Carroll
Genetics: prostate cancer.
Canadian family physician Médecin de famille canadien 2009;55(7):710.
2009: Heather Dorman; Wendy S Meschino; Judith Allanson; Sean M Blaine; Carol Cremin; Clare A Gibbons; Christina Honeywell; Joanne Permaul; June C Carroll
Genetics: Alzheimer disease.
Canadian family physician Médecin de famille canadien 2009;55(6):603.
2009: Hillel Aviezer; Shlomo Bentin; Ran R Hassin; Wendy S Meschino; Jeanne Kennedy; Sonya Grewal; Sherali Esmail; Sharon Cohen; Morris Moscovitch
Not on the face alone: perception of contextualized face expressions in Huntington's disease.
Brain : a journal of neurology 2009;132(Pt 6):1633-44.
2009: June C Carroll; Clare A Gibbons; Sean M Blaine; Carol Cremin; Heather Dorman; Christina Honeywell; Wendy S Meschino; Joanne Permaul; Judith Allanson
Genetics: newborn screening for MCAD deficiency.
Canadian family physician Médecin de famille canadien 2009;55(5):487.
2009: Clare A Gibbons; Sean M Blaine; Judith Allanson; Carol Cremin; Heather Dorman; Christina Honeywell; Wendy S Meschino; Joanne Permaul; June C Carroll
Genetics: Codeine metabolism.
Canadian family physician Médecin de famille canadien 2009;55(2):164.
2009: Judith Allanson; Christina Honeywell; Sean M Blaine; Carol Cremin; Heather Dorman; Clare A Gibbons; Jeremy Grimshaw; Wendy S Meschino; Joanne Permaul; Brenda J Wilson; June C Carroll
Genetics: hereditary hemochromatosis.
Canadian family physician Médecin de famille canadien 2009;55(1):53.
2007: Wendy S Meschino
Fetal Alert Network: Surveying congenital anomalies.
Paediatrics & child health 2007;12(5):365-6.
2007: Douglas E Horsman; Brenda J Wilson; Denise Avard; Wendy S Meschino; Charmaine Kim-Sing; Marie Plante; Andrea Eisen; Heather E Howley; Jacques Simard
Clinical management recommendations for surveillance and risk-reduction strategies for hereditary breast and ovarian cancer among individuals carrying a deleterious BRCA1 or BRCA2 mutation.
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstétrique et gynécologie du Canada : JOGC 2007;29(1):45-60.
2006: Mario Masellis; Parastoo Momeni; Wendy S Meschino; Reid Heffner; Joshua Elder; Christine Sato; Yan Liang; Peter St George-Hyslop; John Hardy; Juan Bilbao; Sandra Black; Ekaterina Rogaeva
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.
Brain : a journal of neurology 2006;129(Pt 11):3115-23.
2005: Joan L Bottorff; Sean Blaine; June C Carroll; Mary Jane Esplen; Jane Evans; Mary Lou Nicolson Klimek; Wendy S Meschino; Paul Ritvo
The educational needs and professional roles of Canadian physicians and nurses regarding genetic testing and adult onset hereditary disease.
Community genetics 2005;8(2):80-7.
2004: Ellen Warner; Donald B Plewes; Kimberley A Hill; Petrina A Causer; Judit Zubovits; Roberta A Jong; Margaret R Cutrara; Gerrit DeBoer; Martin J Yaffe; Sandra J Messner; Wendy S Meschino; Cameron A Piron; Steven A Narod
Surveillance of BRCA1 and BRCA2 mutation carriers with magnetic resonance imaging, ultrasound, mammography, and clinical breast examination.
JAMA : the journal of the American Medical Association 2004;292(11):1317-25.
2004: Wendy S Meschino
Genetics and insurance.
CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2004;171(5):432.
2004: Douglas R Stewart; Alina Huang; Francesca Faravelli; Britt-Marie Anderlid; Livija Medne; Karen L Ciprero; Maninder Kaur; Elena Rossi; Romano Tenconi; Magnus Nordenskjöld; Karen W Gripp; Linda Nicholson; Wendy S Meschino; Esther Capua; Oliver W J Quarrell; Jonathon Flint; Mira Irons; Philip F Giampietro; David B Schowalter; Christina Zaleski; Michela Malacarne; Elaine H Zackai; Nancy B Spinner; Ian D Krantz
Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome.
American journal of medical genetics. Part A 2004;128A(4):340-51.
2004: Isabelle Thiffault; Nancy Hamel; T Pal; Susan McVety; Victoria A Marcus; David Farber; Shannon Cowie; Jean Deschênes; Wendy S Meschino; Fabrice Odefrey; David E Goldgar; T Graham; Steven A Narod; A Kevin Watters; Elizabeth MacNamara; Desirée Du Sart; George Chong; William D Foulkes
Germline truncating mutations in both MSH2 and BRCA2 in a single kindred.
British journal of cancer 2004;90(2):483-91.
2003: S Creighton; Elisabeth W Almqvist; D Macgregor; B Fernandez; H Hogg; J Beis; J Philip Welch; C Riddell; R Lokkesmoe; M Khalifa; J MacKenzie; A Sajoo; S Farrell; F Robert; A Shugar; A Summers; Wendy S Meschino; D Allingham-Hawkins; T Chiu; A Hunter; J Allanson; H Hare; J Schween; L Collins; S Sanders; C Greenberg; S Cardwell; Edmond G Lemire; Patrick M MacLeod; Michael R Hayden
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
Clinical genetics 2003;63(6):462-75.
2003: Wendy S Meschino
The child with developmental delay: An approach to etiology.
Paediatrics & child health 2003;8(1):16-9.
2003: Ellen Warner; June C Carroll; Ruth E Heisey; Vivek Goel; Wendy S Meschino; H Lavina A Lickley; Brian D Doan; Pamela L Chart; Vanessa Orr; Shelley Lothian
Educating women about breast cancer. An intervention for women with a family history of breast cancer.
Canadian family physician Médecin de famille canadien 2003;49():56-63.
2002: Kathy Chun; Ahmad S Teebi; Jack H Jung; Shelley Kennedy; Rachel Laframboise; Wendy S Meschino; Kazuhiko Nakabayashi; Stephen W Scherer; Peter N Ray; Ikuko Teshima
Genetic analysis of patients with the Saethre-Chotzen phenotype.
American journal of medical genetics 2002;110(2):136-43.
2001: LS Di Prospero; M Seminsky; J Honeyford; Brian D Doan; Edmee Franssen; Wendy S Meschino; Pamela L Chart; Ellen Warner
Psychosocial issues following a positive result of genetic testing for BRCA1 and BRCA2 mutations: findings from a focus group and a needs-assessment survey.
CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2001;164(7):1005-9.
2000: K A Phillips; Ellen Warner; Wendy S Meschino; Jon Hunter; Mohamed Abdolell; Gord Glendon; Irene L Andrulis; P J Goodwin
Perceptions of Ashkenazi Jewish breast cancer patients on genetic testing for mutations in BRCA1 and BRCA2.
Clinical genetics 2000;57(5):376-83.
1999: William D Foulkes; Jean-Sebastien Brunet; Ellen Warner; P J Goodwin; Wendy S Meschino; Steven A Narod; P E Goss; Gord Glendon
The importance of a family history of breast cancer in predicting the presence of a BRCA mutation.
American journal of human genetics 1999;65(6):1776-9.
1999: Ellen Warner; William D Foulkes; P Goodwin; Wendy S Meschino; John Blondal; C Paterson; Hilmi Ozcelik; P Goss; D Allingham-Hawkins; Nancy Hamel; LS Di Prospero; V Contiga; C Serruya; M Klein; Roxana Moslehi; J Honeyford; Alexander Liede; Gord Glendon; Jean-Sebastien Brunet; Steven A Narod
Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer.
Journal of the National Cancer Institute 1999;91(14):1241-7.
1997: Elisabeth W Almqvist; S Adam; M Bloch; A Fuller; P Welch; D Eisenberg; D Whelan; D Macgregor; Wendy S Meschino; Michael R Hayden
Risk reversals in predictive testing for Huntington disease.
American journal of human genetics 1997;61(4):945-52.