Ingram CJ - Search Results

1

Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group.

Ingram CJ, Raga TO, Tarekegn A, Browning SL, Elamin MF, Bekele E, Thomas MG, Weale ME, Bradman N, Swallow DM. Ingram CJ, et al. J Mol Evol. 2009 Dec;69(6):579-88. doi: 10.1007/s00239-009-9301-y. Epub 2009 Nov 24. J Mol Evol. 2009. PMID: 19937006

2

A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?

Ingram CJ, Elamin MF, Mulcare CA, Weale ME, Tarekegn A, Raga TO, Bekele E, Elamin FM, Thomas MG, Bradman N, Swallow DM. Ingram CJ, et al. Hum Genet. 2007 Feb;120(6):779-88. doi: 10.1007/s00439-006-0291-1. Epub 2006 Nov 21. Hum Genet. 2007. PMID: 17120047

3

Lactose digestion and the evolutionary genetics of lactase persistence.

Ingram CJ, Mulcare CA, Itan Y, Thomas MG, Swallow DM. Ingram CJ, et al. Hum Genet. 2009 Jan;124(6):579-91. doi: 10.1007/s00439-008-0593-6. Epub 2008 Nov 26. Hum Genet. 2009. PMID: 19034520

4

A worldwide correlation of lactase persistence phenotype and genotypes.

Itan Y, Jones BL, Ingram CJ, Swallow DM, Thomas MG. Itan Y, et al. Among authors: ingram cj. BMC Evol Biol. 2010 Feb 9;10:36. doi: 10.1186/1471-2148-10-36. BMC Evol Biol. 2010. PMID: 20144208 Free PMC article.

5

Group-based pharmacogenetic prediction: is it feasible and do current NHS England ethnic classifications provide appropriate data?

Ingram CJE, Ekong R, Ansari-Pour N, Bradman N, Swallow DM. Ingram CJE, et al. Pharmacogenomics J. 2021 Feb;21(1):47-59. doi: 10.1038/s41397-020-0175-0. Epub 2020 Jul 18. Pharmacogenomics J. 2021. PMID: 32683419

6

Analysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosis.

Ingram CJ, Weale ME, Plaster CA, Morrison KE, Goodall EF, Pall HS, Beck M, Jablonka S, Sendtner M, Fisher EM, Bradman N, Kasperavičiūtė D. Ingram CJ, et al. Amyotroph Lateral Scler. 2012 Jun;13(4):341-6. doi: 10.3109/17482968.2012.654394. Epub 2012 Mar 13. Amyotroph Lateral Scler. 2012. PMID: 22409358

7

Pitfalls in LightCycler diagnosis of the single-nucleotide polymorphism 13.9 kb upstream of the lactase gene that is associated with adult-type hypolactasia.

Weiskirchen R, Tag CG, Mengsteab S, Gressner AM, Ingram CJ, Swallow DM. Weiskirchen R, et al. Among authors: ingram cj. Clin Chim Acta. 2007 Sep;384(1-2):93-8. doi: 10.1016/j.cca.2007.06.008. Epub 2007 Jun 16. Clin Chim Acta. 2007. PMID: 17651714

8

Common inherited mitochondrial DNA mutations and nucleoside reverse transcriptase inhibitor-induced severe hyperlactataemia in HIV-infected adults: an exploratory study.

Arenas-Pinto A, Weller I, Ekong R, Grant A, Karstaedt A, Reiss P, Telisinghe L, Weber R, Bolhaar M, Bradman N, Ingram C. Arenas-Pinto A, et al. Antivir Ther. 2012;17(2):275-82. doi: 10.3851/IMP1947. Epub 2011 Nov 7. Antivir Ther. 2012. PMID: 22293466

9

Evaluation of a novel reverse-hybridization StripAssay for typing DNA variants useful in diagnosis of adult-type hypolactasia.

Tag CG, Oberkanins C, Kriegshäuser G, Ingram CJ, Swallow DM, Gressner AM, Ledochowski M, Weiskirchen R. Tag CG, et al. Among authors: ingram cj. Clin Chim Acta. 2008 Jun;392(1-2):58-62. doi: 10.1016/j.cca.2008.03.006. Epub 2008 Mar 18. Clin Chim Acta. 2008. PMID: 18396155

10

Multidisciplinary Lessons from Palliative Extubations at Home.

Breyre AM, Grammatico M, Policastro A, Ingram CJ, Prisc E, Sussman LS, Couturier K. Breyre AM, et al. Among authors: ingram cj. Prehosp Emerg Care. 2024 Nov 15:1-4. doi: 10.1080/10903127.2024.2420198. Online ahead of print. Prehosp Emerg Care. 2024. PMID: 39475704

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