Seidman C - Search Results

1

Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.

LeMaire SA, McDonald ML, Guo DC, Russell L, Miller CC 3rd, Johnson RJ, Bekheirnia MR, Franco LM, Nguyen M, Pyeritz RE, Bavaria JE, Devereux R, Maslen C, Holmes KW, Eagle K, Body SC, Seidman C, Seidman JG, Isselbacher EM, Bray M, Coselli JS, Estrera AL, Safi HJ, Belmont JW, Leal SM, Milewicz DM. LeMaire SA, et al. Among authors: seidman jg, seidman c. Nat Genet. 2011 Sep 11;43(10):996-1000. doi: 10.1038/ng.934. Nat Genet. 2011. PMID: 21909107 Free PMC article.

2

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families.

Chou YH, Brown EM, Levi T, Crowe G, Atkinson AB, Arnqvist HJ, Toss G, Fuleihan GE, Seidman JG, Seidman CE. Chou YH, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1992 Jul;1(4):295-300. doi: 10.1038/ng0792-295. Nat Genet. 1992. PMID: 1302026

3

Sporadic hypertrophic cardiomyopathy due to de novo myosin mutations.

Watkins H, Thierfelder L, Hwang DS, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. J Clin Invest. 1992 Nov;90(5):1666-71. doi: 10.1172/JCI116038. J Clin Invest. 1992. PMID: 1430197 Free PMC article.

4

cis-dominance of rat atrial natriuretic factor gene regulatory sequences in transgenic mice.

Seidman CE, Schmidt EV, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Can J Physiol Pharmacol. 1991 Oct;69(10):1486-92. doi: 10.1139/y91-223. Can J Physiol Pharmacol. 1991. PMID: 1723347

5

Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy.

Seidman CE, Seidman JG. Seidman CE, et al. Among authors: seidman jg. Mol Biol Med. 1991 Apr;8(2):159-66. Mol Biol Med. 1991. PMID: 1806760 Review.

6

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE. Ho C, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1995 Dec;11(4):389-94. doi: 10.1038/ng1295-389. Nat Genet. 1995. PMID: 7493018

7

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1995 Dec;11(4):434-7. doi: 10.1038/ng1295-434. Nat Genet. 1995. PMID: 7493025

8

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation.

Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG. Pollak MR, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1994 Nov;8(3):303-7. doi: 10.1038/ng1194-303. Nat Genet. 1994. PMID: 7874174

9

A dinucleotide repeat polymorphism in the MYBPH gene.

Watkins H, MacRae CA, Fischman DA, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Hum Mol Genet. 1994 Dec;3(12):2267. doi: 10.1093/hmg/3.12.2267. Hum Mol Genet. 1994. PMID: 7881442 No abstract available.

10

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Among authors: seidman jg, seidman ce. Nat Genet. 1993 Apr;3(4):333-7. doi: 10.1038/ng0493-333. Nat Genet. 1993. PMID: 7981753

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