Alexander S. Whitehead - Publications

Affiliations: 
University of Pennsylvania, Philadelphia, PA, United States 
Area:
Genetics, Cell Biology

84 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Huang J, Liu Y, Vitale S, Penning TM, Whitehead AS, Blair IA, Vachani A, Clapper ML, Muscat JE, Lazarus P, Scheet P, Moore JH, Chen Y. On meta- and mega-analyses for gene-environment interactions. Genetic Epidemiology. PMID 29110346 DOI: 10.1002/gepi.22085  0.48
2016 Bagley SJ, Vitale S, Zhang S, Aggarwal C, Evans TL, Alley EW, Cohen RB, Langer CJ, Blair IA, Vachani A, Whitehead AS. Pretreatment Red Blood Cell Total Folate Concentration Is Associated With Response to Pemetrexed in Stage IV Nonsquamous Non-Small-cell Lung Cancer. Clinical Lung Cancer. PMID 27863923 DOI: 10.1016/j.cllc.2016.10.010  0.48
2016 Zanetti KA, Wang Z, Aldrich M, Amos CI, Blot WJ, Bowman ED, Burdette L, Cai Q, Caporaso N, Chung CC, Gillanders EM, Haiman CA, Hansen HM, Henderson BE, Kolonel LN, ... ... Whitehead AS, et al. Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Lung Cancer (Amsterdam, Netherlands). 98: 33-42. PMID 27393504 DOI: 10.1016/j.lungcan.2016.05.008  0.48
2014 Summers CM, Hammons AL, Arora J, Zhang S, Jochems J, Blair IA, Whitehead AS. Methotrexate modulates folate phenotype and inflammatory profile in EA.hy 926 cells. European Journal of Pharmacology. 732: 60-7. PMID 24657277 DOI: 10.1016/j.ejphar.2014.03.004  0.48
2013 Baldwin DA, Sarnowski CP, Reddy SA, Blair IA, Clapper M, Lazarus P, Li M, Muscat JE, Penning TM, Vachani A, Whitehead AS. Development of a genotyping microarray for studying the role of gene-environment interactions in risk for lung cancer. Journal of Biomolecular Techniques : Jbt. 24: 198-217. PMID 24294113 DOI: 10.7171/jbt.13-2404-004  0.48
2012 Hammons AL, Summers CM, Jochems J, Arora JS, Zhang S, Blair IA, Whitehead AS. Pemetrexed alters folate phenotype and inflammatory profile in EA.hy 926 cells grown under low-folate conditions. European Journal of Pharmacology. 696: 12-7. PMID 22975265 DOI: 10.1016/j.ejphar.2012.08.008  0.48
2010 Stanisławska-Sachadyn A, Woodside JV, Sayers CM, Yarnell JW, Young IS, Evans AE, Mitchell LE, Whitehead AS. The transcobalamin (TCN2) 776C>G polymorphism affects homocysteine concentrations among subjects with low vitamin B(12) status. European Journal of Clinical Nutrition. 64: 1338-43. PMID 20808328 DOI: 10.1038/ejcn.2010.157  0.48
2010 Summers CM, Mitchell LE, Stanislawska-Sachadyn A, Baido SF, Blair IA, Von Feldt JM, Whitehead AS. Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 679-88. PMID 20544798 DOI: 10.1002/bdra.20683  0.48
2009 StanisÅ‚awska-Sachadyn A, Mitchell LE, Woodside JV, Buckley PT, Kealey C, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women. Annals of Human Genetics. 73: 484-91. PMID 19650776 DOI: 10.1111/j.1469-1809.2009.00529.x  0.48
2009 Hammons AL, Summers CM, Woodside JV, McNulty H, Strain JJ, Young IS, Murray L, Boreham CA, Scott JM, Mitchell LE, Whitehead AS. Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1. Clinical Immunology (Orlando, Fla.). 133: 132-7. PMID 19625220 DOI: 10.1016/j.clim.2009.06.008  0.48
2009 Mitchell LE, Morales M, Khartulyari S, Huang Y, Murphy K, Mei M, Von Feldt JM, Blair IA, Whitehead AS. Folate and homocysteine phenotypes: Comparative findings using research and clinical laboratory data. Clinical Biochemistry. 42: 1275-81. PMID 19427846 DOI: 10.1016/j.clinbiochem.2009.04.014  0.48
2009 Lu ZY, Jensen LE, Huang Y, Kealey C, Blair IA, Whitehead AS. The up-regulation of monocyte chemoattractant protein-1 (MCP-1) in Ea.hy 926 endothelial cells under long-term low folate stress is mediated by the p38 MAPK pathway. Atherosclerosis. 205: 48-54. PMID 19152916 DOI: 10.1016/j.atherosclerosis.2008.12.008  0.48
2008 Lu ZY, Morales M, Khartulyari S, Mei M, Murphy KM, Stanislawska-Sachadyn A, Summers CM, Huang Y, Von Feldt JM, Blair IA, Mitchell LE, Whitehead AS. Genetic and biochemical determinants of serum concentrations of monocyte chemoattractant protein-1, a potential neural tube defect risk factor. Birth Defects Research. Part a, Clinical and Molecular Teratology. 82: 736-41. PMID 18937353 DOI: 10.1002/bdra.20507  0.48
2008 Summers CM, Cucchiara AJ, Nackos E, Hammons AL, Mohr E, Whitehead AS, Von Feldt JM. Functional polymorphisms of folate-metabolizing enzymes in relation to homocysteine concentrations in systemic lupus erythematosus. The Journal of Rheumatology. 35: 2179-86. PMID 18785313 DOI: 10.3899/jrheum.080071  0.48
2008 Huang Y, Khartulyari S, Morales ME, Stanislawska-Sachadyn A, Von Feldt JM, Whitehead AS, Blair IA. Quantification of key red blood cell folates from subjects with denned MTHFR 677C>T genotypes using stable isotope dilution liquid chromatography/mass spectrometry Rapid Communications in Mass Spectrometry. 22: 2403-2412. PMID 18634122 DOI: 10.1002/rcm.3624  0.48
2008 Schelleman H, Chen J, Chen Z, Christie J, Newcomb CW, Brensinger CM, Price M, Whitehead AS, Kealey C, Thorn CF, Samaha FF, Kimmel SE. Dosing algorithms to predict warfarin maintenance dose in Caucasians and African Americans. Clinical Pharmacology and Therapeutics. 84: 332-9. PMID 18596683 DOI: 10.1038/clpt.2008.101  0.48
2008 Summers CM, Hammons AL, Mitchell LE, Woodside JV, Yarnell JW, Young IS, Evans A, Whitehead AS. Influence of the cystathionine beta-synthase 844ins68 and methylenetetrahydrofolate reductase 677C>T polymorphisms on folate and homocysteine concentrations. European Journal of Human Genetics : Ejhg. 16: 1010-3. PMID 18398434 DOI: 10.1038/ejhg.2008.69  0.48
2008 StanisÅ‚awska-Sachadyn A, Brown KS, Mitchell LE, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. An insertion/deletion polymorphism of the dihydrofolate reductase (DHFR) gene is associated with serum and red blood cell folate concentrations in women. Human Genetics. 123: 289-95. PMID 18247058 DOI: 10.1007/s00439-008-0475-y  0.48
2008 StanisÅ‚awska-Sachadyn A, Woodside JV, Brown KS, Young IS, Murray L, McNulty H, Strain JJ, Boreham CA, Scott JM, Whitehead AS, Mitchell LE. Evidence for sex differences in the determinants of homocysteine concentrations. Molecular Genetics and Metabolism. 93: 355-62. PMID 18180190 DOI: 10.1016/j.ymgme.2007.11.004  0.48
2008 Kimmel SE, Christie J, Kealey C, Chen Z, Price M, Thorn CF, Brensinger CM, Newcomb CW, Whitehead AS. Apolipoprotein E genotype and warfarin dosing among Caucasians and African Americans. The Pharmacogenomics Journal. 8: 53-60. PMID 17325732 DOI: 10.1038/sj.tpj.6500445  0.48
2007 Casley WL, Ogrodowczyk C, Larocque L, Jaentschke B, LeBlanc-Westwood C, Menzies JA, Whitehouse L, Hefford MA, Aubin RA, Thorn CF, Whitehead AS, Li X. Cytotoxic doses of ketoconazole affect expression of a subset of hepatic genes Journal of Toxicology and Environmental Health - Part a: Current Issues. 70: 1946-1955. PMID 17966066 DOI: 10.1080/15287390701551407  0.48
2007 Laing ME, Dicker P, Moloney FJ, Ho WL, Murphy GM, Conlon P, Whitehead AS, Shields DC. Association of methylenetetrahydrofolate reductase polymorphism and the risk of squamous cell carcinoma in renal transplant patients. Transplantation. 84: 113-6. PMID 17627246 DOI: 10.1097/01.tp.0000266069.41882.28  0.48
2007 Brown KS, Nackos E, Morthala S, Jensen LE, Whitehead AS, Von Feldt JM. Monocyte chemoattractant protein-1: Plasma concentrations and A(-2518)G promoter polymorphism of its gene in systemic lupus erythematosus Journal of Rheumatology. 34: 740-746. PMID 17407231  0.48
2007 Schelleman H, Chen Z, Kealey C, Whitehead AS, Christie J, Price M, Brensinger CM, Newcomb CW, Thorn CF, Samaha FF, Kimmel SE. Warfarin response and vitamin K epoxide reductase complex 1 in African Americans and Caucasians. Clinical Pharmacology and Therapeutics. 81: 742-7. PMID 17329985 DOI: 10.1038/sj.clpt.6100144  0.48
2007 Kealey C, Chen Z, Christie J, Thorn CF, Whitehead AS, Price M, Samaha FF, Kimmel SE. Warfarin and cytochrome P450 2C9 genotype: possible ethnic variation in warfarin sensitivity. Pharmacogenomics. 8: 217-25. PMID 17324110 DOI: 10.2217/14622416.8.3.217  0.48
2007 Huang Y, Lu ZY, Brown KS, Whitehead AS, Blair IA. Quantification of intracellular homocysteine by stable isotope dilution liquid chromatography/tandem mass spectrometry. Biomedical Chromatography : Bmc. 21: 107-12. PMID 17121413 DOI: 10.1002/bmc.735  0.48
2006 StanisÅ‚awska-Sachadyn A, Jensen LE, Kealey C, Woodside JV, Young IS, Scott JM, Murray L, Boreham CA, McNulty H, Strain JJ, Whitehead AS. Association between the NAT1 1095C > A polymorphism and homocysteine concentration. American Journal of Medical Genetics. Part A. 140: 2374-7. PMID 17036310 DOI: 10.1002/ajmg.a.31475  0.48
2006 Von Feldt JM, Scalzi LV, Cucchiara AJ, Morthala S, Kealey C, Flagg SD, Genin A, Van Dyke AL, Nackos E, Chander A, Gehrie E, Cron RQ, Whitehead AS. Homocysteine levels and disease duration independently correlate with coronary artery calcification in patients with systemic lupus erythematosus. Arthritis and Rheumatism. 54: 2220-7. PMID 16802358 DOI: 10.1002/art.21967  0.48
2006 Jensen LE, Hoess K, Mitchell LE, Whitehead AS. Loss of function polymorphisms in NAT1 protect against spina bifida. Human Genetics. 120: 52-7. PMID 16680433 DOI: 10.1007/s00439-006-0181-6  0.48
2006 Jensen LE, Etheredge AJ, Brown KS, Mitchell LE, Whitehead AS. Maternal genotype for the monocyte chemoattractant protein 1 A(-2518)G promoter polymorphism is associated with the risk of spina bifida in offspring. American Journal of Medical Genetics. Part A. 140: 1114-8. PMID 16596675 DOI: 10.1002/ajmg.a.31212  0.48
2006 Brown KS, Huang Y, Lu ZY, Jian W, Blair IA, Whitehead AS. Mild folate deficiency induces a proatherosclerotic phenotype in endothelial cells. Atherosclerosis. 189: 133-41. PMID 16469322 DOI: 10.1016/j.atherosclerosis.2005.12.018  0.48
2005 Jensen LE, Hoess K, Whitehead AS, Mitchell LE. The NAT1 C1095A polymorphism, maternal multivitamin use and smoking, and the risk of spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 73: 512-6. PMID 15959877 DOI: 10.1002/bdra.20143  0.48
2004 Kelly CB, McDonnell AP, Johnston TG, Mulholland C, Cooper SJ, McMaster D, Evans A, Whitehead AS. The MTHFR C677T polymorphism is associated with depressive episodes in patients from Northern Ireland. Journal of Psychopharmacology (Oxford, England). 18: 567-71. PMID 15582924 DOI: 10.1177/0269881104047285  0.48
2004 Mitchell LE, Adzick NS, Melchionne J, Pasquariello PS, Sutton LN, Whitehead AS. Spina bifida. Lancet (London, England). 364: 1885-95. PMID 15555669 DOI: 10.1016/S0140-6736(04)17445-X  0.48
2004 Jensen LE, Whitehead AS. The 3′ untranslated region of the membrane-bound IL-1R accessory protein mRNA confers tissue-specific destabilisation Journal of Immunology. 173: 6248-6258. PMID 15528363  0.48
2004 Jensen LE, Barbaux S, Hoess K, Fraterman S, Whitehead AS, Mitchell LE. The human T locus and spina bifida risk. Human Genetics. 115: 475-82. PMID 15449172 DOI: 10.1007/s00439-004-1185-8  0.48
2004 Kane D, Jensen LE, Grehan S, Whitehead AS, Bresnihan B, Fitzgerald O. Quantitation of metalloproteinase gene expression in rheumatoid and psoriatic arthritis synovial tissue distal and proximal to the cartilage-pannus junction. The Journal of Rheumatology. 31: 1274-80. PMID 15229943  0.48
2004 Jensen LE, Wall AM, Cook M, Hoess K, Thorn CF, Whitehead AS, Mitchell LE. A common ABCC2 promoter polymorphism is not a determinant of the risk of spina bifida. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 396-9. PMID 15211708 DOI: 10.1002/bdra.20023  0.48
2004 Brown KS, Kluijtmans LA, Young IS, Murray L, McMaster D, Woodside JV, Yarnell JW, Boreham CA, McNulty H, Strain JJ, McPartlin J, Scott JM, Mitchell LE, Whitehead AS. The 5,10-methylenetetrahydrofolate reductase C677T polymorphism interacts with smoking to increase homocysteine. Atherosclerosis. 174: 315-22. PMID 15136061 DOI: 10.1016/j.atherosclerosis.2004.01.023  0.48
2004 Brown KS, Cook M, Hoess K, Whitehead AS, Mitchell LE. Evidence that the risk of spina bifida is influenced by genetic variation at the NOS3 locus. Birth Defects Research. Part a, Clinical and Molecular Teratology. 70: 101-6. PMID 15039923 DOI: 10.1002/bdra.20002  0.48
2004 Brown KS, Kluijtmans LA, Young IS, McNulty H, Mitchell LE, Yarnell JW, Woodside JV, Boreham CA, McMaster D, Murray L, Strain JJ, Whitehead AS. The thymidylate synthase tandem repeat polymorphism is not associated with homocysteine concentrations in healthy young subjects. Human Genetics. 114: 182-5. PMID 14586640 DOI: 10.1007/s00439-003-1039-9  0.48
2003 Jensen LE, Whitehead AS. Ubiquitin activated tumor necrosis factor receptor associated factor-6 (TRAF6) is recycled via deubiquitination Febs Letters. 553: 190-194. PMID 14550571 DOI: 10.1016/S0014-5793(03)00998-0  0.48
2003 Jensen LE, Whitehead AS. Pellino3, a novel member of the pellino protein family, promotes activation of c-Jun and Elk-1 and may act as a scaffolding protein Journal of Immunology. 171: 1500-1506. PMID 12874243  0.48
2003 Jensen LE, Whitehead AS. ELAM-1/E-selectin promoter contains an inducible AP-1/CREB site and is not NF-κB-specific Biotechniques. 35: 54-58. PMID 12866405  0.48
2003 Jensen LE, Whitehead AS. Pellino2 activates the mitogen activated protein kinase pathway Febs Letters. 545: 199-202. PMID 12804775 DOI: 10.1016/S0014-5793(03)00533-7  0.48
2003 Jensen LE, Whitehead AS. Expression of alternatively spliced interleukin-1 receptor accessory protein mRNAs is differentially regulated during inflammation and apoptosis Cellular Signalling. 15: 793-802. PMID 12781872 DOI: 10.1016/S0898-6568(03)00039-1  0.48
2003 Brown KS, Kluijtmans LA, Young IS, Woodside J, Yarnell JW, McMaster D, Murray L, Evans AE, Boreham CA, McNulty H, Strain JJ, Mitchell LE, Whitehead AS. Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1014-20. PMID 12689917 DOI: 10.1161/01.ATV.0000071348.70527.F4  0.48
2003 Meleady R, Ueland PM, Blom H, Whitehead AS, Refsum H, Daly LE, Vollset SE, Donohue C, Giesendorf B, Graham IM, Ulvik A, Zhang Y, Bjorke Monsen AL. Thermolabile methylenetetrahydrofolate reductase, homocysteine, and cardiovascular disease risk: the European Concerted Action Project. The American Journal of Clinical Nutrition. 77: 63-70. PMID 12499324  0.48
2002 Doolin MT, Barbaux S, McDonnell M, Hoess K, Whitehead AS, Mitchell LE. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. American Journal of Human Genetics. 71: 1222-6. PMID 12375236 DOI: 10.1086/344209  0.48
2001 Rygg M, Uhlar CM, Thorn C, Jensen LE, Gaughan DJ, Varley AW, Munford RS, Göke R, Chen Y, Whitehead AS. In vitro evaluation of an enhanced human serum amyloid A (SAA2) promoter-regulated soluble TNF receptor fusion protein for anti-inflammatory gene therapy. Scandinavian Journal of Immunology. 53: 588-95. PMID 11422907 DOI: 10.1046/j.1365-3083.2001.00919.x  0.48
2001 Jensen LE, Whitehead AS. IRAK1b, a Novel Alternative Splice Variant of Interleukin-1 Receptor-associated Kinase (IRAK), Mediates Interleukin-1 Signaling and Has Prolonged Stability Journal of Biological Chemistry. 276: 29037-29044. PMID 11397809 DOI: 10.1074/jbc.M103815200  0.48
2001 Cahill M, Karabatzaki M, Donoghue C, Meleady R, Mynett-Johnson LA, Mooney D, Graham IM, Whitehead AS, Shields DC. Thermolabile MTHFR genotype and retinal vascular occlusive disease. The British Journal of Ophthalmology. 85: 88-90. PMID 11133719 DOI: 10.1136/bjo.85.1.88  0.48
2000 Shields DC, Ramsbottom D, Donoghue C, Pinjon E, Kirke PN, Molloy AM, Edwards YH, Mills JL, Mynett-Johnson L, Weir DG, Scott JM, Whitehead AS. Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury). American Journal of Medical Genetics. 92: 206-11. PMID 10817656 DOI: 10.1002/(SICI)1096-8628(20000529)92:3<206::AID-AJMG9>3.0.CO;2-W  0.48
2000 Jensen LE, Muzio M, Mantovani A, Whitehead AS. IL-1 signaling cascade in liver cells and the involvement of a soluble form of the IL-1 receptor accessory protein Journal of Immunology. 164: 5277-5286. PMID 10799889 DOI: 10.4049/JIMMUNOL.164.10.5277  0.48
1999 Harmon DL, Shields DC, Woodside JV, McMaster D, Yarnell JWG, Young IS, Peng K, Shane B, Evans AE, Whitehead AS. Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations Genetic Epidemiology. 17: 298-309. PMID 10520212 DOI: 10.1002/(SICI)1098-2272(199911)17:4<298::AID-GEPI5>3.0.CO;2-V  0.48
1999 Whitehead AS, Molloy AM, Ramsbottom D, Weir DG, Kirke PN, Mills JL, Gallagher PM, Scott JM. Gene-gene interactions and neural tube defects. Clinical Genetics. 55: 133-4. PMID 10189094 DOI: 10.1034/j.1399-0004.1999.550213.x  0.48
1999 Shields DC, Kirke PN, Mills JL, Ramsbottom D, Molloy AM, Burke H, Weir DG, Scott JM, Whitehead AS. The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. American Journal of Human Genetics. 64: 1045-55. PMID 10090889 DOI: 10.1086/302310  0.48
1999 Harmon DL, Doyle RM, Meleady R, Doyle M, Shields DC, Barry R, Coakley D, Graham IM, Whitehead AS. Genetic analysis of the thermolabile variant of 5,10- methylenetetrahydrofolate reductase as a risk factor for ischemic stroke Arteriosclerosis, Thrombosis, and Vascular Biology. 19: 208-211. PMID 9974399  0.48
1998 Gallagher PM, Naughten E, Hanson NQ, Schwichtenberg K, Bignell M, Yuan M, Ward P, Yap S, Whitehead AS, Tsai MY. Characterization of mutations in the cystathionine beta-synthase gene in Irish patients with homocystinuria. Molecular Genetics and Metabolism. 65: 298-302. PMID 9889017 DOI: 10.1006/mgme.1998.2771  0.48
1998 Jensen LE, Whitehead AS. Competitive reverse transcription polymerase chain reaction for quantifying pre-MRNA and mRNA of major acute phase proteins Journal of Immunological Methods. 215: 45-58. PMID 9744747 DOI: 10.1016/S0022-1759(98)00085-4  0.48
1998 Jensen LE, Whitehead AS. Regulation of serum amyloid A protein expression during the acute-phase response Biochemical Journal. 334: 489-503. PMID 9729453 DOI: 10.1042/BJ3340489  0.48
1998 Adderley S, Fitzgerald D, O'Neill S, Moran N, Smith R, Stephens G, O'Hara AM, Moran AP, Orren A, Hobart MJ, Fernie BA, Connaughton JJ, Walsh AM, O'Connor JJ, Murphy RP, ... ... Whitehead AS, et al. Royal academy of medicine in ireland section of biomedical sciences - Proceedings of meeting held 9th January 1998 Irish Journal of Medical Science. 167: 197-205. DOI: 10.1007/BF02937936  0.48
1997 Kim CE, Gallagher PM, Guttormsen AB, Refsum H, Ueland PM, Ose L, Folling I, Whitehead AS, Tsai MY, Kruger WD. Functional modeling of vitamin responsiveness in yeast: a common pyridoxine-responsive cystathionine beta-synthase mutation in homocystinuria. Human Molecular Genetics. 6: 2213-21. PMID 9361025 DOI: 10.1093/hmg/6.13.2213  0.48
1997 Harmon DL, McMaster D, McCluskey DR, Shields DC, Whitehead AS. A common genetic variant affecting folate metabolism is not over-represented in chronic fatigue syndrome Annals of Clinical Biochemistry. 34: 427-429. PMID 9247678  0.48
1997 Harmon DL, McMaster D, Shields DC, Whitehead AS, Rea IM. MTHFR thermolabile genotype frequencies and longevity in Northern Ireland Atherosclerosis. 131: 137-138. PMID 9180255 DOI: 10.1016/S0021-9150(97)06096-6  0.48
1997 Ramsbottom D, Scott JM, Molloy A, Weir DG, Kirke PN, Mills JL, Gallagher PM, Whitehead AS. Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects? Clinical Genetics. 51: 39-42. PMID 9084933 DOI: 10.1111/j.1399-0004.1997.tb02412.x  0.48
1996 Shields DC, Butler A, Mosurski KR, Walsh MT, Whitehead AS. Mapping genes within a YAC by computer-assisted interpretation of partial restriction digestions Nucleic Acids Research. 24: 4495-4500. PMID 8948640 DOI: 10.1093/nar/24.22.4495  0.48
1996 Steel DM, Donoghue FC, O'Neill RM, Uhlar CM, Whitehead AS. Expression and regulation of constitutive and acute phase serum amyloid A mRNAs in hepatic and non-hepatic cell lines. Scandinavian Journal of Immunology. 44: 493-500. PMID 8947601 DOI: 10.1046/j.1365-3083.1996.d01-341.x  0.48
1996 Gallagher PM, Meleady R, Shields DC, Tan KS, McMaster D, Rozen R, Evans A, Graham IM, Whitehead AS. Homocysteine and risk of premature coronary heart disease: Evidence for a common gene mutation Circulation. 94: 2154-2158. PMID 8901666  0.48
1996 Uhlar CM, Black IL, Shields DC, Brack CM, Schreiber G, Whitehead AS. Wallaby serum amyloid A protein: cDNA cloning, sequence and evolutionary analysis Scandinavian Journal of Immunology. 43: 271-276. PMID 8602460  0.48
1995 Butler A, Rochelle JM, Seldin MF, Whitehead AS. The gene encoding the mouse serum amyloid A protein, apo-SAA5, maps to proximal chromosome 7 Immunogenetics. 42: 153-155. PMID 7607707 DOI: 10.1007/BF00178591  0.48
1995 Gallagher PM, Ward P, Tan S, Naughten E, Kraus JP, Sellar GC, McConnell DJ, Graham I, Whitehead AS. High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients Human Mutation. 6: 177-180. PMID 7581402 DOI: 10.1002/humu.1380060211  0.48
1994 Uhlar CM, Burgess CJ, Sharp PM, Whitehead AS. Evolution of the serum amyloid A (SAA) protein superfamily. Genomics. 19: 228-35. PMID 8188253 DOI: 10.1006/geno.1994.1052  0.48
1994 Sellar GC, Jordan SA, Bickmore WA, Fantes JA, Van Heyningen V, Whitehead AS. The human serum amyloid A protein (SAA) superfamily gene cluster: Mapping to chromosome 11p15.1 by physical and genetic linkage analysis Genomics. 19: 221-227. PMID 8188252 DOI: 10.1006/geno.1994.1051  0.48
1994 Seery LT, McCabe BD, Schoenberg DR, Whitehead AS. S-adenosyl-L-homocysteine hydrolase from Xenopus laevis--identification, developmental expression and evolution. Biochemical and Biophysical Research Communications. 205: 1539-46. PMID 7811234 DOI: 10.1006/bbrc.1994.2842  0.48
1993 Rubio N, Sharp PM, Rits M, Zahedi K, Whitehead AS. Structure, expression, and evolution of guinea pig serum amyloid P component and C-reactive protein Journal of Biochemistry. 113: 277-284. PMID 8486600  0.48
1993 Seery LT, Schoenberg DR, Barbaux S, Sharp PM, Whitehead AS. Identification of a novel member of the pentraxin family in Xenopus laevis Proceedings of the Royal Society B: Biological Sciences. 253: 263-270. PMID 7694301  0.48
1993 Sellar GC, Keane J, Mehdi H, Peeples ME, Browne N, Whitehead AS. Characterization and Acute-Phase Modulation of Canine Apolipoprotein H (β2-Glycoprotein 1) Biochemical and Biophysical Research Communications. 191: 1288-1293. PMID 7682067 DOI: 10.1006/bbrc.1993.1357  0.48
1991 Mehdi H, Nunn M, Steel DM, Whitehead AS, Perez M, Walker L, Peeples ME. Nucleotide sequence and expression of the human gene encoding apolipoprotein H (β2-glycoprotein I) Gene. 108: 293-298. PMID 1748314 DOI: 10.1016/0378-1119(91)90449-L  0.48
1990 Shelley CS, Remold-O'Donnell E, Rosen FS, Whitehead AS. Structure of the human sialophorin (CD43) gene. Identification of features atypical of genes encoding integral membrane proteins. The Biochemical Journal. 270: 569-76. PMID 2241892 DOI: 10.1042/bj2700569  0.48
1988 Whitehead AS, Rits M, Michaelson J. Molecular genetics of mouse serum amyloid P component (SAP): cloning and gene mapping Immunogenetics. 28: 388-390. PMID 3169883 DOI: 10.1007/BF00364241  0.48
1987 Falus A, Wakeland EK, McConnell TJ, Gitlin J, Whitehead AS, Colten HR. DNA polymorphism of MHC III genes in inbred and wild mouse strains Immunogenetics. 25: 290-298. PMID 2883115 DOI: 10.1007/BF00404421  0.48
1987 Rao AG, Howard OMZ, Ng SC, Whitehead AS, Colten HR, Sodetz JM. Complementary DNA and derived amino acid sequence of the α subunit of human complement protein C8: Evidence for the existence of a separate α subunit messenger RNA Biochemistry. 26: 3556-3564. PMID 2820471  0.48
1984 Whitehead AS, Woods DE, Fleischnick E, Chin JE, Yunis EJ, Katz AJ, Gerald PS, Alper CA, Colten HR. DNA polymorphism of the C4 genes. A new marker for analysis of the major histocompatibility complex New England Journal of Medicine. 310: 88-91. PMID 6581384 DOI: 10.1056/NEJM198401123100204  0.48
Show low-probability matches.