Collins FS - Search Results

1

MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability.

Lipkin SM, Wang V, Jacoby R, Banerjee-Basu S, Baxevanis AD, Lynch HT, Elliott RM, Collins FS. Lipkin SM, et al. Among authors: collins fs. Nat Genet. 2000 Jan;24(1):27-35. doi: 10.1038/71643. Nat Genet. 2000. PMID: 10615123

2

Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers.

Lipkin SM, Wang V, Stoler DL, Anderson GR, Kirsch I, Hadley D, Lynch HT, Collins FS. Lipkin SM, et al. Among authors: collins fs. Hum Mutat. 2001 May;17(5):389-96. doi: 10.1002/humu.1114. Hum Mutat. 2001. PMID: 11317354

3

Characterization of the CHD family of proteins.

Woodage T, Basrai MA, Baxevanis AD, Hieter P, Collins FS. Woodage T, et al. Among authors: collins fs. Proc Natl Acad Sci U S A. 1997 Oct 14;94(21):11472-7. doi: 10.1073/pnas.94.21.11472. Proc Natl Acad Sci U S A. 1997. PMID: 9326634 Free PMC article.

4

Mutations in the human Jagged1 gene are responsible for Alagille syndrome.

Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoli DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC. Oda T, et al. Among authors: collins fs. Nat Genet. 1997 Jul;16(3):235-42. doi: 10.1038/ng0797-235. Nat Genet. 1997. PMID: 9207787

5

Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis.

Hacia JG, Brody LC, Chee MS, Fodor SP, Collins FS. Hacia JG, et al. Among authors: collins fs. Nat Genet. 1996 Dec;14(4):441-7. doi: 10.1038/ng1296-441. Nat Genet. 1996. PMID: 8944024

6

Somatic mutation of the MEN1 gene in parathyroid tumours.

Heppner C, Kester MB, Agarwal SK, Debelenko LV, Emmert-Buck MR, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Doppman JL, Alexander RH, Kim YS, Saggar SK, Lubensky IA, Zhuang Z, Liotta LA, Chandrasekharappa SC, Collins FS, Spiegel AM, Burns AL, Marx SJ. Heppner C, et al. Among authors: collins fs. Nat Genet. 1997 Aug;16(4):375-8. doi: 10.1038/ng0897-375. Nat Genet. 1997. PMID: 9241276

7

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals.

Struewing JP, Abeliovich D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC. Struewing JP, et al. Among authors: collins fs. Nat Genet. 1995 Oct;11(2):198-200. doi: 10.1038/ng1095-198. Nat Genet. 1995. PMID: 7550349

8

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.

Hacia JG, Fan JB, Ryder O, Jin L, Edgemon K, Ghandour G, Mayer RA, Sun B, Hsie L, Robbins CM, Brody LC, Wang D, Lander ES, Lipshutz R, Fodor SP, Collins FS. Hacia JG, et al. Among authors: collins fs. Nat Genet. 1999 Jun;22(2):164-7. doi: 10.1038/9674. Nat Genet. 1999. PMID: 10369258

9

Evolutionary sequence comparisons using high-density oligonucleotide arrays.

Hacia JG, Makalowski W, Edgemon K, Erdos MR, Robbins CM, Fodor SP, Brody LC, Collins FS. Hacia JG, et al. Among authors: collins fs. Nat Genet. 1998 Feb;18(2):155-8. doi: 10.1038/ng0298-155. Nat Genet. 1998. PMID: 9462745

10

A high-density microsatellite map of the ataxia-telangiectasia locus.

Vanagaite L, James MR, Rotman G, Savitsky K, Bar-Shira A, Gilad S, Ziv Y, Uchenik V, Sartiel A, Collins FS, Sheffield VC, Richard CW 3rd, Weissenbach J, Shiloh Y. Vanagaite L, et al. Among authors: collins fs. Hum Genet. 1995 Apr;95(4):451-4. doi: 10.1007/BF00208975. Hum Genet. 1995. PMID: 7705845

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