Farrer LA - Search Results

1

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.

Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, Sebastiani P, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. Farrell JJ, et al. Among authors: farrer la. Blood. 2011 May 5;117(18):4935-45. doi: 10.1182/blood-2010-11-317081. Epub 2011 Mar 8. Blood. 2011. PMID: 21385855 Free PMC article.

2

Linkage of early-onset osteoarthritis and chondrocalcinosis to human chromosome 8q.

Baldwin CT, Farrer LA, Adair R, Dharmavaram R, Jimenez S, Anderson L. Baldwin CT, et al. Among authors: farrer la. Am J Hum Genet. 1995 Mar;56(3):692-7. Am J Hum Genet. 1995. PMID: 7887424 Free PMC article.

3

Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.

Farrer LA, Arnos KS, Asher JH Jr, Baldwin CT, Diehl SR, Friedman TB, Greenberg J, Grundfast KM, Hoth C, Lalwani AK, et al. Farrer LA, et al. Am J Hum Genet. 1994 Oct;55(4):728-37. Am J Hum Genet. 1994. PMID: 7942851 Free PMC article.

4

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.

Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B. Baldwin CT, et al. Among authors: farrer la. Hum Mol Genet. 1995 Sep;4(9):1637-42. doi: 10.1093/hmg/4.9.1637. Hum Mol Genet. 1995. PMID: 8541853

5

A novel mutation in the MITF gene causes Waardenburg syndrome type 2.

Lautenschlager NT, Milunsky A, DeStefano A, Farrer L, Baldwin CT. Lautenschlager NT, et al. Genet Anal. 1996 Jul;13(2):43-4. doi: 10.1016/1050-3862(95)00148-4. Genet Anal. 1996. PMID: 8880147

6

Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.

DeStefano AL, Baldwin CT, Burzstyn M, Gavras I, Handy DE, Joost O, Martel T, Nicolaou M, Schwartz F, Streeten DH, Farrer LA, Gavras H. DeStefano AL, et al. Among authors: farrer la. Am J Hum Genet. 1998 Nov;63(5):1425-30. doi: 10.1086/302096. Am J Hum Genet. 1998. PMID: 9792870 Free PMC article.

7

Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.

Baima J, Nicolaou M, Schwartz F, DeStefano AL, Manolis A, Gavras I, Laffer C, Elijovich F, Farrer L, Baldwin CT, Gavras H. Baima J, et al. Hypertension. 1999 Jul;34(1):4-7. doi: 10.1161/01.hyp.34.1.4. Hypertension. 1999. PMID: 10406815

8

Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension.

Baldwin CT, Schwartz F, Baima J, Burzstyn M, DeStefano AL, Gavras I, Handy DE, Joost O, Martel T, Manolis A, Nicolaou M, Bresnahan M, Farrer L, Gavras H. Baldwin CT, et al. Am J Hypertens. 1999 Sep;12(9 Pt 1):853-7. doi: 10.1016/s0895-7061(99)00070-9. Am J Hypertens. 1999. PMID: 10509541

9

Genetic predisposition to stroke in relatives of hypertensives.

Nicolaou M, DeStefano AL, Gavras I, Cupples LA, Manolis AJ, Baldwin CT, Gavras H, Farrer LA. Nicolaou M, et al. Among authors: farrer la. Stroke. 2000 Feb;31(2):487-92. doi: 10.1161/01.str.31.2.487. Stroke. 2000. PMID: 10657427

10

Maternal component in the familial aggregation of hypertension.

DeStefano AL, Gavras H, Heard-Costa N, Bursztyn M, Manolis A, Farrer LA, Baldwin CT, Gavras I, Schwartz F. DeStefano AL, et al. Among authors: farrer la. Clin Genet. 2001 Jul;60(1):13-21. doi: 10.1034/j.1399-0004.2001.600103.x. Clin Genet. 2001. PMID: 11531965

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