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Michael Woods

Research Profile

Geographic Areas

Newfoundland and Labrador

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Disorders

Physiology

Phenomena

Founder Effect

Chemicals & Drugs

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Publications

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Erica Clarke; Jane S Green; Roger C Green; Krista Mahoney; Patrick S Parfrey; H Banfield Younghusband; Michael O Woods
Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.
Bridget A Fernandez; Sara Fernandez; Jane S Green; Andrée MacMillan; Krista Mahoney; Sarah McColl; Sergio L Pereira; Proton Rahman; Stephen W Scherer; Michael O Woods; Brendan Barrett; Kym M Boycott; Ford Bursey
Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.
Bridget A Fernandez; Dzintra Fernandez; George Fox; Fady Kamel; Krista Mahoney; Barbara Noble; Patrick S Parfrey; Eric Sala; Susan Stuckless; Rick Bhatia; Nash Denic; Amanda Dohey; Nigel Duguid; Laura Edwards; Michael O Woods
A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features.

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All Publications

2012: Erica Clarke; Jane S Green; Roger C Green; Krista Mahoney; Patrick S Parfrey; H Banfield Younghusband; Michael O Woods
Inherited deleterious variants in GALNT12 are associated with CRC susceptibility.
Human mutation 2012;33(7):1056-8.
2012: Bridget A Fernandez; Sara Fernandez; Jane S Green; Andrée MacMillan; Krista Mahoney; Sarah McColl; Sergio L Pereira; Proton Rahman; Stephen W Scherer; Michael O Woods; Brendan Barrett; Kym M Boycott; Ford Bursey
Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.
BMC medical genetics 2012;13():111.
2012: Bridget A Fernandez; Dzintra Fernandez; George Fox; Fady Kamel; Krista Mahoney; Barbara Noble; Patrick S Parfrey; Eric Sala; Susan Stuckless; Rick Bhatia; Nash Denic; Amanda Dohey; Nigel Duguid; Laura Edwards; Michael O Woods
A Newfoundland cohort of familial and sporadic idiopathic pulmonary fibrosis patients: clinical and genetic features.
Respiratory research 2012;13():64.
2009: Roger C Green; Patrick S Parfrey; Michael O Woods; H Banfield Younghusband
Prediction of Lynch syndrome in consecutive patients with colorectal cancer.
Journal of the National Cancer Institute 2009;101(5):331-40.
2007: Peter Campbell; Laura Edwards; John R McLaughlin; Jane Green; H Banfield Younghusband; Michael O Woods
Cytochrome P450 17A1 and catechol O-methyltransferase polymorphisms and age at Lynch syndrome colon cancer onset in Newfoundland.
Clinical cancer research : an official journal of the American Association for Cancer Research 2007;13(13):3783-8.
2007: Michael O Woods; Phillip Williams; Amanda Careen; Laura Edwards; Sylvia Bartlett; John R McLaughlin; H Banfield Younghusband
A new variant database for mismatch repair genes associated with Lynch syndrome.
Human mutation 2007;28(7):669-73.
2007: Susan Stuckless; Patrick S Parfrey; Michael O Woods; Janet Cox; G William Fitzgerald; Jane S Green; Roger C Green
The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome.
Familial cancer 2007;6(1):1-12.
2005: Michael O Woods; Angela J Hyde; Fiona K Curtis; Susan Stuckless; Jane S Green; Aaron F Pollett; J Desmond Robb; Roger C Green; Marina E Croitoru; Amanda Careen; Jason A W Chaulk; Jegan Jegathesan; John R McLaughlin; Steven Gallinger; H Banfield Younghusband; Bharati Bapat; Patrick S Parfrey
High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.
Clinical cancer research : an official journal of the American Association for Cancer Research 2005;11(19 Pt 1):6853-61.
2001: Philip L Beales; Nicholas Katsanis; R A Lewis; Stephen J Ansley; Nursel Elcioglu; J Raza; Michael O Woods; Jane S Green; Patrick S Parfrey; William S Davidson; James R Lupski
Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci.
American journal of human genetics 2001;68(3):606-16.
2000: Nicholas Katsanis; Philip L Beales; Michael O Woods; R A Lewis; Jane S Green; Patrick S Parfrey; Stephen J Ansley; William S Davidson; James R Lupski
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome.
Nature genetics 2000;26(1):67-70.
1999: TL Young; Michael O Woods; Patrick S Parfrey; Jane S Green; Donna Hefferton; William S Davidson
A founder effect in the newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM.
American journal of human genetics 1999;65(6):1680-7.
1999: TL Young; L Penney; Michael O Woods; Patrick S Parfrey; Jane S Green; Donna Hefferton; William S Davidson
A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31.
American journal of human genetics 1999;64(3):900-4.
1999: Michael O Woods; TL Young; Patrick S Parfrey; Donna Hefferton; Jane S Green; William S Davidson
Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus.
Genomics 1999;55(1):2-9.
1998: TL Young; Michael O Woods; Patrick S Parfrey; Jane S Green; E O'Leary; Donna Hefferton; William S Davidson
Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.
American journal of medical genetics 1998;78(5):461-7.