Simpson SA - Search Results

1

A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis.

Hayward C, Swingler RJ, Simpson SA, Brock DJ. Hayward C, et al. Among authors: simpson sa. Am J Hum Genet. 1996 Nov;59(5):1165-7. Am J Hum Genet. 1996. PMID: 8900247 Free PMC article. No abstract available.

2

Superoxide dismutase mutations in an unselected cohort of Scottish amyotrophic lateral sclerosis patients.

Jones CT, Swingler RJ, Simpson SA, Brock DJ. Jones CT, et al. Among authors: simpson sa. J Med Genet. 1995 Apr;32(4):290-2. doi: 10.1136/jmg.32.4.290. J Med Genet. 1995. PMID: 7643359 Free PMC article.

3

Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees.

Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A, Armstrong C, Bierut LJ, Reich T, Detera-Wadleigh SD, Goldin LR, Badner JA, Guroff JJ, Gershon ES, McMahon FJ, Simpson S, MacKinnon D, McInnis M, Stine OC, DePaulo JR, Blehar MC, Nurnberger JI Jr. Foroud T, et al. Am J Med Genet. 2000 Feb 7;96(1):18-23. Am J Med Genet. 2000. PMID: 10686547

4

Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype.

Friddle C, Koskela R, Ranade K, Hebert J, Cargill M, Clark CD, McInnis M, Simpson S, McMahon F, Stine OC, Meyers D, Xu J, MacKinnon D, Swift-Scanlan T, Jamison K, Folstein S, Daly M, Kruglyak L, Marr T, DePaulo JR, Botstein D. Friddle C, et al. Am J Hum Genet. 2000 Jan;66(1):205-15. doi: 10.1086/302697. Am J Hum Genet. 2000. PMID: 10631152 Free PMC article.

5

Huntington disease in black African populations.

Scrimgeour EM, Simpson SA. Scrimgeour EM, et al. Among authors: simpson sa. Hum Genet. 1992 Sep-Oct;90(1-2):186-7. doi: 10.1007/BF00210775. Hum Genet. 1992. PMID: 1427779 No abstract available.

6

Allelic and locus heterogeneity in inherited venous malformations.

Calvert JT, Riney TJ, Kontos CD, Cha EH, Prieto VG, Shea CR, Berg JN, Nevin NC, Simpson SA, Pasyk KA, Speer MC, Peters KG, Marchuk DA. Calvert JT, et al. Among authors: simpson sa. Hum Mol Genet. 1999 Jul;8(7):1279-89. doi: 10.1093/hmg/8.7.1279. Hum Mol Genet. 1999. PMID: 10369874

7

Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity.

Calvert JT, Burns S, Riney TJ, Sahoo T, Orlow SJ, Nevin NC, Haisley-Royster C, Prose N, Simpson SA, Speer MC, Marchuk DA. Calvert JT, et al. Among authors: simpson sa. Hum Hered. 2001;51(3):180-2. doi: 10.1159/000053340. Hum Hered. 2001. PMID: 11173970

8

Interstitial deletion of chromosome 13: prognosis and adult phenotype.

Dean JC, Simpson S, Couzin DA, Stephen GS. Dean JC, et al. J Med Genet. 1991 Aug;28(8):533-5. doi: 10.1136/jmg.28.8.533. J Med Genet. 1991. PMID: 1920369 Free PMC article.

9

Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation.

Batstone PJ, Simpson S, Bonthron DT, Keng WT, Hamilton D, Forsyth L, Sales M, Pratt N, Goudie D. Batstone PJ, et al. Am J Med Genet A. 2003 Apr 30;118A(3):241-6. doi: 10.1002/ajmg.a.10204. Am J Med Genet A. 2003. PMID: 12673654

10

Ambient Teens Sleep Study: Protocol for a co-produced feasibility study in adolescents using a contactless radar-based sleep sensor.

Caddick L, Gaggioni G, Haughton D, Brown J, Inchley J, Simpson SA, Lyall LM, Murray A, Romaniuk L, Krondorf L, Lopez LM, Smith DJ, Wyse C, Whalley H. Caddick L, et al. Among authors: simpson sa. PLoS One. 2024 Nov 14;19(11):e0313286. doi: 10.1371/journal.pone.0313286. eCollection 2024. PLoS One. 2024. PMID: 39541279 Free PMC article.

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