Multipoint analysis of human quantitative genetic variation.

Por Goldgar, D E
Publicado em 1990

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

Por Goldgar, D E, Oniki, R S
Publicado em 1992

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

Por Goldgar, D E, Easton, D F
Publicado em 1997

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

Por Goldgar, D E, Thompson, E A
Publicado em 1988

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

Por Goldgar, D E, Fain, P R
Publicado em 1988

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

Por Goldgar, D E, Green, P, Parry, D M, Mulvihill, J J
Publicado em 1989

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

Por Jefferies, S, Edwards, S M, Hamoudi, R A, A'Hern, R, Foulkes, W, Goldgar, D, Eeles, R
Publicado em 2001

Dinucleotide repeat polymorphism at the D17S513 locus

Por Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.
Publicado em 1991

Dinucleotide repeat polymorphism at the D17S514 locus

Por Oliphant, A.R., Wright, E.C., Swensen, J., Gruis, N.A., Goldgar, D., Skolnick, M.H.
Publicado em 1991

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

Por Parsons, M, Thompson, B, Goldgar, D, Hopper, J, Jenkins, M, Buchanan, D, Young, J, Spurdle, A
Publicado em 2012

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

Por Kerkhofs, C. H. H., Spurdle, A. B., Lindsey, P. J., Goldgar, D. E., Gómez-García, E. B.
Publicado no Hered Cancer Clin Pract (2016)

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

Por Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F
Publicado em 1989

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

Por Narod, S, Ford, D, Devilee, P, Barkardottir, R B, Eyfjord, J, Lenoir, G, Serova, O, Easton, D, Goldgar, D
Publicado em 1995

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

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

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

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

A genomic search for linkage of neurofibromatosis to RFLPs.

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

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

Por 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
Publicado em 1997

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

Por McKay, J, Thompson, D, Lesueur, F, Stankov, K, Pastore, A, Watfah, C, Strolz, S, Riccabona, G, Moncayo, R, Romeo, G, Goldgar, D
Publicado em 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...

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

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

Por 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
Publicado em 2012