Multipoint analysis of human quantitative genetic variation.

von Goldgar, D E
Veröffentlicht 1990

Comparison of a multipoint identity-by-descent method with parametric multipoint linkage analysis for mapping quantitative traits.

von Goldgar, D E, Oniki, R S
Veröffentlicht 1992

Optimal strategies for mapping complex diseases in the presence of multiple loci.

von Goldgar, D E, Easton, D F
Veröffentlicht 1997

Bayesian interval estimation of genetic relationships: application to paternity testing.

von Goldgar, D E, Thompson, E A
Veröffentlicht 1988

Models of multilocus recombination: nonrandomness in chiasma number and crossover positions.

von Goldgar, D E, Fain, P R
Veröffentlicht 1988

Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.

von Goldgar, D E, Green, P, Parry, D M, Mulvihill, J J
Veröffentlicht 1989

No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours

von Jefferies, S, Edwards, S M, Hamoudi, R A, A'Hern, R, Foulkes, W, Goldgar, D, Eeles, R
Veröffentlicht 2001

Dinucleotide repeat polymorphism at the D17S513 locus

von Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.
Veröffentlicht 1991

Dinucleotide repeat polymorphism at the D17S514 locus

von Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.
Veröffentlicht 1991

Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance

von Parsons, M, Thompson, B, Goldgar, D, Hopper, J, Jenkins, M, Buchanan, D, Young, J, Spurdle, A
Veröffentlicht 2012

Assessing biases of information contained in pedigrees for the classification of BRCA-genetic variants: a study arising from the ENIGMA analytical working group

von Kerkhofs, C. H. H., Spurdle, A. B., Lindsey, P. J., Goldgar, D. E., Gómez-García, E. B.
Veröffentlicht in Hered Cancer Clin Pract (2016)

Refined physical and genetic mapping of the NF1 region on chromosome 17.

von Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F
Veröffentlicht 1989

Genetic heterogeneity of breast-ovarian cancer revisited. Breast Cancer Linkage Consortium.

von Narod, S, Ford, D, Devilee, P, Barkardottir, R B, Eyfjord, J, Lenoir, G, Serova, O, Easton, D, Goldgar, D
Veröffentlicht 1995

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

von Puget, N, Sinilnikova, O M, Stoppa-Lyonnet, D, Audoynaud, C, Pagès, S, Lynch, H T, Goldgar, D, Lenoir, G M, Mazoyer, S
Veröffentlicht 1999

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

von Stern, H J, Saal, H M, Lee, J S, Fain, P R, Goldgar, D E, Rosenbaum, K N, Barker, D F
Veröffentlicht 1992

A genomic search for linkage of neurofibromatosis to RFLPs.

von Barker, D, Wright, E, Nguyen, K, Cannon, L, Fain, P, Goldgar, D, Bishop, D T, Carey, J, Kivlin, J, Willard, H
Veröffentlicht 1987

Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

von Serova, O M, Mazoyer, S, Puget, N, Dubois, V, Tonin, P, Shugart, Y Y, Goldgar, D, Narod, S A, Lynch, H T, Lenoir, G M
Veröffentlicht 1997

Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer

von McKay, J, Thompson, D, Lesueur, F, Stankov, K, Pastore, A, Watfah, C, Strolz, S, Riccabona, G, Moncayo, R, Romeo, G, Goldgar, D
Veröffentlicht 2004

Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonin...

von Schuffenecker, I, Ginet, N, Goldgar, D, Eng, C, Chambe, B, Boneu, A, Houdent, C, Pallo, D, Schlumberger, M, Thivolet, C, Lenoir, G M
Veröffentlicht 1997

The challenges of finding the gene responsible for a rare, autosomal dominant gastric cancer susceptibility syndrome

von Li, JJ, Healey, S, Phillips, K, Makunin, I, Wayte, N, Schrader, I, Worthley, D, Lindor, N, Huntsman, D, Goldgar, D, Suthers, G, Chenevix-Trench, G
Veröffentlicht 2012