Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 22

1.

Placing negative multi-gene panel results into clinical context.

Hermel DJ, McKinnon WC, Wood ME, Greenblatt MS.

Fam Cancer. 2017 Oct;16(4):595. doi: 10.1007/s10689-017-9974-0. No abstract available.

PMID:
28455554
2.

Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program.

Hermel DJ, McKinnon WC, Wood ME, Greenblatt MS.

Fam Cancer. 2017 Jan;16(1):159-166. doi: 10.1007/s10689-016-9913-5.

PMID:
27401692
3.

Universal Versus Targeted Screening for Lynch Syndrome: Comparing Ascertainment and Costs Based on Clinical Experience.

Erten MZ, Fernandez LP, Ng HK, McKinnon WC, Heald B, Koliba CJ, Greenblatt MS.

Dig Dis Sci. 2016 Oct;61(10):2887-2895. doi: 10.1007/s10620-016-4218-y. Epub 2016 Jul 6.

PMID:
27384051
4.

The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype.

Kwok CT, Vogelaar IP, van Zelst-Stams WA, Mensenkamp AR, Ligtenberg MJ, Rapkins RW, Ward RL, Chun N, Ford JM, Ladabaum U, McKinnon WC, Greenblatt MS, Hitchins MP.

Eur J Hum Genet. 2014 May;22(5):617-24. doi: 10.1038/ejhg.2013.200. Epub 2013 Oct 2.

5.

Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors.

Riley BD, Culver JO, Skrzynia C, Senter LA, Peters JA, Costalas JW, Callif-Daley F, Grumet SC, Hunt KS, Nagy RS, McKinnon WC, Petrucelli NM, Bennett RL, Trepanier AM.

J Genet Couns. 2012 Apr;21(2):151-61. doi: 10.1007/s10897-011-9462-x. Epub 2011 Dec 2.

PMID:
22134580
6.

Life after BRCA1/2 testing: family communication and support issues.

DeMarco TA, McKinnon WC.

Breast Dis. 2006-2007;27:127-36. Review.

PMID:
17917144
7.

Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study.

Park JG, Kim DW, Hong CW, Nam BH, Shin YK, Hong SH, Kim IJ, Lim SB, Aronson M, Bisgaard ML, Brown GJ, Burn J, Chow E, Conrad P, Douglas F, Dunlop M, Ford J, Greenblatt MS, Heikki J, Heinimann K, Lynch EL, Macrae F, McKinnon WC, Möeslein G, Rossi BM, Rozen P, Schofield L, Vaccaro C, Vasen H, Velthuizen M, Viel A, Wijnen J; International Society for Gastrointestinal Hereditary Tumours.

Clin Cancer Res. 2006 Jun 1;12(11 Pt 1):3389-93.

8.

Genetic testing for breast and ovarian cancer susceptibility: a family experience.

Van Riper M, McKinnon WC.

J Midwifery Womens Health. 2004 May-Jun;49(3):210-9. Review.

PMID:
15134674
9.

Identifying women at risk for inherited breast cancer using a mammography registry.

Geller BM, Mickey RM, Rairikar CJ, McKinnon WC.

J Cancer Educ. 2001 Spring;16(1):46-9.

PMID:
11270900
10.

Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1.

Bourdeau A, Cymerman U, Paquet ME, Meschino W, McKinnon WC, Guttmacher AE, Becker L, Letarte M.

Am J Pathol. 2000 Mar;156(3):911-23.

11.

Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors.

McKinnon WC, Baty BJ, Bennett RL, Magee M, Neufeld-Kaiser WA, Peters KF, Sawyer JC, Schneider KA.

JAMA. 1997 Oct 15;278(15):1217-20. No abstract available.

PMID:
9333247
12.

The Familial Cancer Program of the Vermont Cancer Center: Development of a Cancer Genetics Program in a Rural Area.

McKinnon WC, Guttmacher AE, Greenblatt MS, Compas BE, May S, Cutler RE, Yandell DW.

J Genet Couns. 1997 Jun;6(2):131-45. doi: 10.1023/A:1025603900839.

PMID:
26142091
13.

Von Hippel-Lindau disease presenting as pancreatic neuroendocrine tumour.

Mount SL, Weaver DL, Taatjes DJ, McKinnon WC, Hebert JC.

Virchows Arch. 1995;426(5):523-8.

PMID:
7633663
14.

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J, et al.

Nat Genet. 1994 Dec;8(4):345-51.

PMID:
7894484
15.

Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

McAllister KA, Lennon F, Bowles-Biesecker B, McKinnon WC, Helmbold EA, Markel DS, Jackson CE, Guttmacher AE, Pericak-Vance MA, Marchuk DA.

J Med Genet. 1994 Dec;31(12):927-32.

16.

Hereditary hemorrhagic telangiectasia: a disorder in search of the genetics community.

Guttmacher AE, McKinnon WC, Upton MD.

Am J Med Genet. 1994 Aug 15;52(2):252-3. No abstract available.

PMID:
7802026
17.

A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34.

McDonald MT, Papenberg KA, Ghosh S, Glatfelter AA, Biesecker BB, Helmbold EA, Markel DS, Zolotor A, McKinnon WC, Vanderstoep JL, et al.

Nat Genet. 1994 Feb;6(2):197-204.

PMID:
8162075
18.
19.

Effect of nocodazole on vesicular traffic to the apical and basolateral surfaces of polarized MDCK cells.

Breitfeld PP, McKinnon WC, Mostov KE.

J Cell Biol. 1990 Dec;111(6 Pt 1):2365-73.

20.
21.

Transepithelial transport of immunoglobulins: a model of protein sorting and transcytosis.

Breitfeld PP, Casanova JE, Simister NE, Ross SA, McKinnon WC, Mostov KE.

Am J Respir Cell Mol Biol. 1989 Oct;1(4):257-62. Review. No abstract available.

PMID:
2696513
22.

Sorting signals.

Breitfeld PP, Casanova JE, Simister NE, Ross SA, McKinnon WC, Mostov KE.

Curr Opin Cell Biol. 1989 Aug;1(4):617-23. Review. No abstract available.

PMID:
2576381

Supplemental Content

Loading ...
Support Center