Liddell M - Search Results

1

Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease.

Kehoe PG, Russ C, McIlory S, Williams H, Holmans P, Holmes C, Liolitsa D, Vahidassr D, Powell J, McGleenon B, Liddell M, Plomin R, Dynan K, Williams N, Neal J, Cairns NJ, Wilcock G, Passmore P, Lovestone S, Williams J, Owen MJ. Kehoe PG, et al. Among authors: liddell m. Nat Genet. 1999 Jan;21(1):71-2. doi: 10.1038/5009. Nat Genet. 1999. PMID: 9916793 No abstract available.

2

No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease.

Liddell MB, Bayer AJ, Owen MJ. Liddell MB, et al. Hum Mol Genet. 1995 May;4(5):853-8. doi: 10.1093/hmg/4.5.853. Hum Mol Genet. 1995. PMID: 7633445

3

Genetic risk of Alzheimer's disease: advising relatives.

Liddell MB, Lovestone S, Owen MJ. Liddell MB, et al. Br J Psychiatry. 2001 Jan;178(1):7-11. doi: 10.1192/bjp.178.1.7. Br J Psychiatry. 2001. PMID: 11136203 Review.

4

Role of amyloid beta-protein in Alzheimer's disease.

Liddell M, Owen MJ. Liddell M, et al. Lancet. 1992 Oct 3;340(8823):851. Lancet. 1992. PMID: 1357270 No abstract available.

5

Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease.

Liddell M, Williams J, Bayer A, Kaiser F, Owen M. Liddell M, et al. J Med Genet. 1994 Mar;31(3):197-200. doi: 10.1136/jmg.31.3.197. J Med Genet. 1994. PMID: 8014966 Free PMC article.

6

Alzheimer's disease.

Owen M, Liddell M, McGuffin P. Owen M, et al. Among authors: liddell m. BMJ. 1994 Mar 12;308(6930):672-3. doi: 10.1136/bmj.308.6930.672. BMJ. 1994. PMID: 8142788 Free PMC article. No abstract available.

7

Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease.

Kehoe P, Williams J, Holmans P, Liddell M, Lovestone S, Holmes C, Powell J, Neal J, Wilcock G, Owen MJ. Kehoe P, et al. Among authors: liddell m. Neuroreport. 1996 Sep 2;7(13):2155-8. doi: 10.1097/00001756-199609020-00019. Neuroreport. 1996. PMID: 8930979

8

Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease.

Harold D, Peirce T, Moskvina V, Myers A, Jones S, Hollingworth P, Moore P, Lovestone S, Powell J, Foy C, Archer N, Walter S, Edmonson A, McIlroy S, Craig D, Passmore PA, Goate A, Hardy J, O'Donovan M, Williams J, Liddell M, Owen MJ, Jones L. Harold D, et al. Among authors: liddell m. Hum Genet. 2003 Aug;113(3):258-67. doi: 10.1007/s00439-003-0960-2. Epub 2003 May 21. Hum Genet. 2003. PMID: 12759818

9

Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual.

Peake IR, Liddell MB, Moodie P, Standen G, Mancuso DJ, Tuley EA, Westfield LA, Sorace JM, Sadler JE, Verweij CL, et al. Peake IR, et al. Among authors: liddell mb. Blood. 1990 Feb 1;75(3):654-61. Blood. 1990. PMID: 2297569 Free article.

10

Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms.

Moodie P, Liddell MB, Peake IR, Bloom AL. Moodie P, et al. Among authors: liddell mb. Br J Haematol. 1988 Sep;70(1):77-84. doi: 10.1111/j.1365-2141.1988.tb02437.x. Br J Haematol. 1988. PMID: 2902876

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