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Angela Brooks-Wilson Publications

by Stephanie McInnis — last modified Nov 03, 2011 02:57 PM
Angela Brooks-Wilson Complete Bibliography

  1. Starczynowski DT, Vercauteren S, Sung S, Brooks-Wilson A, Lam WL, Karsan A. Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes. Leukemia research. 2011 Apr 25;35:444 -7.

  2. Smedby KE, Foo JN, Skibola CF, Darabi H, Conde L, Hjalgrim H, Kumar V, Chang ET, Rothman N, Cerhan JR, Brooks-Wilson AR, Rehnberg E, Irwan ID, Ryder LP, Brown PN, Bracci PM, Agana L, Riby J, Cozen W, Davis S, Hartge P, Morton LM, Severson RK, Wang SS, SLager SL, Fredericksen ZS, Novak AJ, Kay NE, Habermann TM, Armstrong B, Kricker A, Milliken S, Purdue MP, Vajdic CM, Boyle P, Lan Q, Zahm SH, Zhang Y, Zheng T, Leach S, Spinelli JJ, Smith MT, Chanock SJ, Padyukov L, Alfredsson L, Klareskog L, Glimelius B, Melbye M, Liu ET, Adami H, Humphreys K, Liu J. GWAS of Follicular Lymphoma Reveals Allelic Heterogeneity at 6p21.32 and Suggests Shared Genetic Susceptibility with Diffuse Large B-cell Lymphoma. PLoS Genet. 2011 Apr 1;7(4):e1001378.

  3. Pharoah PDP, Palmieri RT, Ramus SJ, Gayther SA, Andrulis IL, Anton-Vulver HA, Antonenkova N, Antoniou AC, Beattie MS, Beckmann M, Birrer MJ, Bogdanova N, Bolton KL, Brewster W, Brooks-Wilson A, Brown R, Bützow R, Caldes T, Caligo MA, Campbell IG, Chang-Claude J, Chen A, Chenevix-Trench G, Cook LS, Couch FJ, Cramer DW, Cunningham JM, Despierre E, Doherty JA, Dork T, Durst M, Eccles D, Ekici AB, Fasching PA, de Fazio A, Fenstermacher DA, Flanagan JM, Fridley BL, Friedman E, Gao B, Gentry-Maharaj A, Godwin AK, Goode E, Goodman MT, Gross J, Hansen TVO, Harnett PR, Heikkinen T, Hein R, Hogdall CK, Hogdall EV, Iversen E, Jakubowska A, Johnatty SE, Karlan BY, Kauff ND, Kaye SB, Kelemen LE, Kiemeney LA, Kjaer SK, Lambrechts D, Lapolla JP, Lazaro C, Le ND, Leminen A, Leunen K, Levine DA, Lu Y, Lundvall L, Macgregor S, Marees T, Massuger L, McLaughlin JR, Menon U, Montagna M, Moysich KB, Narod S, Nathanson KL, Nedergaard L, Ness RB, Nevanlinna HA, Nickels S, Osorio A, Paul J, Pearce CL, Phelan CM, Pike MC, Radice P, Rossing MA, Schildkraut J, Sellers TA, Singer CF, Song H, Stram DO, Sutphen R, Terry KL, Tsai Y, van Altena AM, Vergote I, Vierkant RA, Vitonis AF, Walsh C, Wang-Gohrke S, Wappenschmidt B, Wu AH, Ziogas A, Berchuck A, Risch HA. The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing. Clin Cancer Res. 2011 Jun 1;17(11):3742-50. [Epub 2011 Mar 8.]

  4. Morin RD, Mendez-Lago M, Mungall AJ, Goya R, Mungall KL, Corbett RD, Johnson NA, Severson TM, Chiu R, Field M, Jackman S, Krzywinski M, Scott DW, Trinh DL, Tamura-Wells J, Li S, Firme MR, Rogic S, Griffith M, Chan S, Yakovenko O, Meyer IM, Zhao EY, Smailus D, Moksa M, Chittaranjan S, Rimsza L, Brooks-Wilson A, Spinelli JJ, Ben-Neriah S, Meissner B, Woolcock B, Boyle M, McDonald H, Tam A, Zhao Y, Delaney A, Zeng T, Tse K, Butterfield Y, Birol I, Holt R, Schein J, Horsman DE, Moore R, Jones SJM, Connors JM, Hirst M, Gascoyne RD, Marra MA. Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma. Nature. 2011 Aug 18;476(7360):298-303.

  5. Beesley J, Pickett HA, Johnatty SE, Dunning AM, Chen X, Li J, Michailidou K, Lu Y, Rider DN, Palmieri RT, Stutz MD, Lambrechts D, Despierre E, Lambrechts S, Vergote I, Chang-Claude J, Nickels S, Vrieling A, Flesch-Janys D, Wang-Gohrke S, Eilber U, Bodanova N, Antonenkova N, Runnebaum IB, Dörk T, Goodman MT, Lurie G, Wilkens LR, Matsuno RK, Kiemeney LA, Aben KKH, Marees T, Massuger LFAG, Fridley BL, Vierkant RA, Bandera EV, Olson SH, Orlow I, Rodriguez-Rodriguez L, Cook LS, Le ND, Brooks-Wilson A, Kelemen LE, Campbell I, Gayther SA, Ramus SJ, Gentry-Maharaj A, Menon U, Ahmed S, Baynes C, Pharoah PD, Muir K, Lophatananon A, Chaiwerawattana A, Wiangnon S, Macgregor S, Easton DF, Reddel RR, Goode EL, Chenevix-Trench G. Functional Polymorphisms in the TERT Promoter Are Associated with Risk of Serous Epithelial Ovarian and Breast Cancers. PLoS ONE. 2011 Jan 1;6(9):e24987.

  6. Bashash M, Hislop TG, Shah AM, Le N, Brooks-Wilson A, Bajdik CD. The prognostic effect of ethnicity for gastric and esophageal cancer: the population-based experience in British Columbia, Canada. BMC cancer. 2011 May 9;11(1):164.

  7. Amankwah EK, Wang Q, Schildkraut JM, Tsai Y, Ramus SJ, Fridley BL, Beesley J, Johnatty SE, Webb PM, Chenevix-Trench G, Dale LC, Lambrechts D, Amant F, Despierre E, Vergote I, Gayther SA, Gentry-Maharaj A, Menon U, Chang-Claude J, Wang-Gohrke S, Anton-Culver H, Ziogas A, Dörk T, Dürst M, Antonenkova N, Bogdanova N, Brown R, Flanagan JM, Kaye SB, Paul J, Bützow R, Nevanlinna H, Campbell I, Eccles DM, Karlan BY, Gross J, Walsh C, Pharoah PDP, Song Honglin, Krüger Kjær S, Høgdall E, Høgdall C, Lundvall L, Nedergaard L, Kiemeney LALM, Massuger LFAG, van Altena AM, Vermeulen SHHM, Le ND, Brooks-Wilson A, Cook LS, Phelan CM, Cunningham JM, Vachon CM, Vierkant RA, Iversen ES, Berchuch A, Goode EL, Sellers TA, Kelemen LE. Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium. PLoS ONE. 2011 Jan 1;6(5):e19642.

  8. Goode EL, Genevix-Trench G, Song H, Ramus SJ, Notaridou M, Lawrenson K, Widschwendter M, Vierkant RA, Larson MC, Kjaer SK, Birrer MJ, Berchuck A, Schildkraut J, Tomlinson I, Kiemeney LA, Cook LS, Gronwald J, Garcia-Closas M, Gore ME, Campbell I, Whittemore AS, Sutphen R, Phelan C, Anton-Culver H, Pearce CL, Lambrechts D, Rossing MA, Chang-Claude J, Moysich KB, Goodman MT, Dörk T, Nevanlinna H, Ness RB, Rafnar T, Hogdall C, Hogdall E, Fridley BL, Cunningham JM, Sieh W, McGuire V, Godwin AK, Cramer DW, Hernandex D, Levine D, Lu K, Iversen ES, Palmieri RT, Houlston R, van Altena AM, Aben KKH, Massuger LFAG, Brooks-Wilson A, Kelemen LE, Le ND, Jakubowska A, Lubinski J, Medrek K, Stafford A, Easton DF, Tyrer J, Bolton KL, Harrington P, Eccles D, Chen A, Molina AN, Davila BN, Arango H, Tsai Y, Chen Z, RIsch HA, McLaughlin J, Narod SA, Ziogas A, Brewster W, Gentry-Maharaj A, Menon U, Wu AH, Stram DO, Pike MC, Beesley J, Webb PM, Chen X, Ekici AB, Thiel FC, Beckmann MW, Yang H, Wentzensen N, Lissowska J, Fasching PA, Despierre E, Amant F, Vergote Ignace, Doherty J, Hein R, Wang-Gohrke S, Lurie G, Carney ME, Thompson PJ, Runnebaum I, Hillemanns P, Dürst M, Antonenkova N, Bogdanova N, Leminen A, Butzow R, Hekkinen T, Stefansson K, Sulem P, Besenbacher S, Sellers TA, Gayther SA, Pharoah PDP. A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. Nature Genetics. 2010 Oct 1;42(10):874-9.

  9. Conde L, Halperin E, Akers NK, Brown KM, Smedby KE, Rothman N, Nieters A, Slager SL, Brooks-Wilson A, Agana L, Riby J, Liu J, Adami H, Darabi H, Hjalgrim H, Low H, Humphreys K, Melbye M, Chang ET, Glimelius B, Cozen W, Davis S, Hartge P, Morton LM, Schenk M, Wang SS, Armstrong B, Kricker A, Milliken S, Purdue MP, Vajdic CM, Boyle P, Lan Q, Zahm SH, Zhang Y, Zheng T, Becker N, Benavente Y, Boffetta Paolo, Brennan P, Butterbach K, Cocco P, Foretova L, Maynadié M, de Sanjosé S, Staines A, Spinelli JJ, Achenbach SJ, Call TG, Camp NJ, Glenn M, Caporaso NE, Cerhan JR, Cunningham JM, Goldin LR, Hanson CA, Kay NE, Lanasa MC, Leis JF, Marti GE, Rabe KG, Rassenti LZ, Spector LG, Strom SS, Vachon CM, Weinberg JB, Holly EA, Chanock S, Smith MT, Bracci PM, Skibola CF. Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Nature Genetics. 2010 Aug 1;42(8):661-4.

  10. Bretherick KL, Bu R, Gascoyne RD, Connors JM, Spinelli JJ, Brooks-Wilson AR. Elevated circulating t(14;18) translocation levels prior to diagnosis of follicular lymphoma. Blood. 2010 Dec 23;116(26):6146-7.

  11. Bashash M, Yavari P, Hislop TG, Shah A, Sadjadi A, Babaei M, Le N, Brooks-Wilson A, Malekzadeh R, Bajdik C. Comparison of Two Diverse Populations, British Columbia, Canada, and Ardabil, Iran, Indicates Several Variables Associated with Gastric and Esophageal Cancer Survival. Journal of Gastrointestinal Cancer. 2010 Nov 20.

  12. Yamada S, Richardson K, Tang M, Moadebi S, Halaschek-Wiener J, Fitzgerald JM, Elwood K,  Marra F* and Brooks-Wilson A*. Genetic Variation in Carboxylesterase Genes and Susceptibility to Isoniazid-induced Hepatotoxicity. Pharmacogenomics J. 2010 Mar 2. [Epub ahead of print].
  13. Skibola CF, Bracci PM, Nieters A, Brooks-Wilson A, de Sanjose S, Hughes AM, Cerhan JR, Skibola DR, Purdue M, Willett E, Lan Q, Foretova L, Schenk M, Spinelli JJ, Slager SL, DeRoos A, Smith MT, Roman E,  Cozen W, Boffetta P, Kricker A, Zheng T, Lightfoot T, Cocco P, Benavente Y, Zhang Y, Hartge T, Linet M, Becker N, Brennan P, Zhang L, Armstrong B, Smith A, Shiao R, Novak AJ, Maynadie M, Chanock S, Staines A, Holford TR, Holly EA, Rothman R, and Wang SS. Tumor necrosis factor (TNF) and lymphotoxin-alpha (LTA) polymorphisms and risk of non-Hodgkin lymphoma in the InterLymph Consortium. American Journal of Epidemiology. 2010 Feb  1;171(3):267-76.
  14. Krajden M, Yu A, Braybrook H, Lai AS, Mak A, Chow R, Cook D, Tellier R, Petric M, Gascoyne RD, Connors JM, Brooks-Wilson AR, Gallagher RP, Spinelli JJ. GBV-C/hepatitis G virus infection and non-hodgkin lymphoma: A case control study. International Journal of Cancer. 2009 Nov 10. [Epub ahead of print]
  15. Schuetz JM, Leach S, MacArthur AC, Lai AS, Gallagher RP, Connors JM, Gascoyne RD, Spinelli JJ, Brooks-Wilson AR. Genetic Variation in the NBS1, MRE11, RAD50 and BLM Genes and Susceptibility to non-Hodgkin Lymphoma (NHL). Accepted by BMC Medical Genetics. 2009 Nov 16;10:117.
  16. Halaschek-Wiener J, Amirabbasi-Beik M, Monfared N, Pieczyk M, Sailer C, Kollar A, Turnbull R, Agalaridis G, Yamada S, Oliveira L, Collins JA, Meneilly G, Marra MA, Madden KM, Le ND, Connors JM and Brooks-Wilson AR. Genetic variation in healthy oldest old. PLoS ONE 2009 Aug 14; 4(8): e6641. doi:10.1371/journal.pone.0006641.
  17. Ng CH , Janoo-Gilani R, Sipahimalani P, Gallagher RP, Gascoyne RD, Connors JM, Weber JP, Lai AS, Leach S, Le ND, Brooks-Wilson AR, Spinelli JJ. Interaction between organochlorines and the AHR gene, and risk of non-Hodgkin lymphoma. Cancer Causes Control. 2009 Sept 26, Epub ahead of print.
  18. Hossain S, Brooks-Wilson A, Le N and Spinelli JJ. Impact of Genotype Misclassification on Genetic Association Estimates and the Bayesian Adjustment. American Journal of Epidemiology. 2009 170(8): 994 - 1004. Epub Sept 26 2009 ahead of print.
  19. Yamada S, Tang M, Richardson K, Halaschek-Wiener J, Chan M, Cook VJ, FitzGerald JM, Elwood RK, Brooks-Wilson A* and Marra F*. Genetic variations of the NAT-2, CYP450 2E1 and isoniazid hepatotoxicity in a diverse population. Accepted by Pharmacogenetics. *These authors co-led the study.
  20. Skibola CF, Bracci PR, Halperin E, Agana L, Craig DW, Conde L, Iyadurai K, Nieters A, Brooks-Wilson AR, Curry JD, Spinelli J, Holly EA, Riby J, Becker N, Smith MT and Brown KM. Genetic variants at 6p21.33 influence follicular lymphoma risk. Nature Genetics. 2009 Aug;41(8):873-5. Epub 2009 Jul 20.
  21. Moore RA, Ogilvie G, Fornika DJ, Moravan V, Amirabbasi-Biek M, Kollar A, Burgess T, Hsu R, Towers L, Lo J, Brisson M, Matisic J and Brooks-Wilson AR. Prevalence and type distribution of human papillomavirus in 5,000 British Columbia women – Implications for vaccination. Cancer Causes Control. 2009 May 29. [Epub ahead of print]
  22. Johnson NA, Boyle M, Bashashati A, Leach S, Brooks-Wilson A, Sehn L, Chhanabhai M, Brinkman RR, Connors JM, Weng AP and Gascoyne RD. Diffuse large B cell lymphoma: reduced CD20 expression is associated with an inferior survival. Blood. 2009 Apr. 16;113(16):3773-80. Epub 2008 Nov 24.
  23. Johnson NA, Leach S, Woolcock B, deLeeuw RJ, Bashashati A, Sehn L, Connors JM, Brooks-Wilson A and Gascoyne RD. CD20 mutations involving the rituximab epitope are rare in diffuse large B cell lymphomas and are not a significant cause of R-CHOP failure. Haematologica 2009 Mar; 94(3):423-7. Epub 2009 Feb 11.
  24. Halaschek-Wiener J, Vulto I, Fornika D, Collins J, Connors J, Le N, Lansdorp PM and Brooks-Wilson A. 2008. Reduced telomere length variation in healthy oldest old. Mechanisms of Ageing and Development. 129 (2008): 638-641.
  25. Starczynowski DT, Vercauteren S, Telenius A, Sung S, Tohyama K, Brooks-Wilson A, Spinelli JJ, Eaves CJ, Eaves AC, Horsman DE, Lam WL and Karsan A. High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival. Blood. 2008 Oct 15;112(8):3412-24. Epub 2008 Jul 28.
  26. Kumar RA, McLean A, Leach S, Bonaguro R, McGee KA, Aguirre-Hennandez R, Abrahams BS, Coccaro EF, Hodgins S, Turecki G, Condon A, Muir W, Brooks-Wilson AR, Blackwood D and Simpson EM. Initial Association of NR2E1 with Bipolar Disorder and Identification of Candidate Mutations in Bipolar Disorder, Schizophrenia and Aggression through Resequencing. Am J Med Genet B Neuropsychiatr. Genet. 2008 Sep 5;147B(6):880-9.
  27. Bashash M, Shah A, Hislop G, Brooks-Wilson A, Le N and Bajdik C. Incidence and Survival of Gastric and Esophageal Cancer Diagnosed in British Columbia, Canada, during 1990-1999. The Canadian Journal of Gastroenterology. 2008 Feb; 22(2):143-8.
  28. Spinelli JJ, Lai AS, Krajden M, Andonov A, Gascoyne RD, Connors JM, Brooks-Wilson AR and Gallagher RP. Hepatitis C virus and risk of non-Hodgkin lymphoma in British Columbia, Canada. Int. J. Cancer. 2008 Feb 1;122(3):630-3.
  29. Spinelli JJ, Ng CH, Weber J-P, Connors JM, Gascoyne RD, Lai AS, Brooks-Wilson AR, Le ND, Berry BR, Gallagher RP. Organochlorines and risk of non-Hodgkin lymphoma. International Journal of Cancer. 2007 Dec 15;121(12):2767-75.
  30. Sipahimalani P; Spinelli J; MacArthur A, Lai A, Connors J, Gascoyne R, Gallagher R and Brooks-Wilson AR. Common Genetic Variation in ATM Does Not Determine Susceptibility to non-Hodgkin Lymphoma. International Journal of Cancer. 2007 Nov 1;121(9):1967-75.
  31. Montgomery SB, Griffith OL, Schuetz JM, Brooks-Wilson A and Jones SJM. A Survey of Genomic Properties for the Detection of Regulatory Polymorphisms. PLoS Computational Biology (2007) 3(6) e106: 1-11.
  32. Novik KL, Spinelli JJ, MacArthur A, Shumansky K, Sipahimalani P, Leach S, Lai A, Connors JM, Gascoyne RD, Gallagher RP, Brooks-Wilson AR. Genetic Variation in H2AFX Contributes to Risk of Lymphoma. Cancer Epidemiology Biomarkers and Prevention 2007. 16(6): 1098-1106.
  33. Kumar RA, Leach S, Bonaguro R, Chen J, Yokom DW, Abrahams BS, Seaver L, Schwartz CE, Dobyns WB, Brooks-Wilson A, and Simpson EM. Mutation and Evolutionary Analyses of Identify NR2E1 Candidate Regulatory Mutations in Humans with Severe Cortical Malformations. Genes, Brain and Behavior 2007. 6: 503-516.
  34. Bajdik CD, Abanto ZU, Spinelli JJ, Brooks-Wilson A, Gallagher RP. Identifying related cancer types based on their incidence among people with multiple cancers. Emerging Themes in Epidemiology 2006. 3:17.
  35. Rothman N, Skibola CF, Wang SS, Morgan G, Lan Q, Smith MT, Spinelli JJ, Willett E, De Sanjose S, Cocco P, Berndt SI, Brennan P, Brooks-Wilson A, Wacholder S, Becker N, Hartge P, Zheng T, Roman E, Holly EA, Boffetta P, Armstrong B, Cozen W, Linet M, Bosch GX, Ennas MG, Holford TR, Gallagher RP, Rollinson S, Bracci PM, Cerhan JR, Whitby D, Moore PS, Leaderer B, Lai A, Spink C, Davis S, Bosch R, Scarpa A, Zhang Y, Severson RK, Yeager-Jeffery M, Chanock S, Nieters A. Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: A report from the InterLymph Consortium. Lancet Oncology 2006. 7(1): 27-38. This paper was the subject of a commentary by G. Salles and B. Coiffier, 2006. Lancet Oncology 7(1): 3-4.
  36. Bajdik CD, Kuo B, Rusaw S, Jones S and Brooks-Wilson A. 2005. CGMIM: Automated text-mining of Online Mendelian Inheritance in Man (OMIM) to identify genetically-associated cancers and candidate genes. BMC Bioinformatics 6:78-84.
  37. Halaschek-Wiener J, Khattra J, McKay S, Pouzyrev A, Stott J, Yang G, Holt R, Jones SM, Marra MA, Brooks-Wilson A* and Riddle D. 2005. Analysis of Long Lived C. Elegans daf-2 Mutants Using Serial Analysis of Gene Expression. Genome Research 15: 603-615. *Corresponding Author
  38. Anglesio MS, Evdokimova V, Melnyk N, Zhang L, Fernandez CV, Grundy PE, Leach S, Marra MA, Brooks-Wilson AR, Penninger J, and Sorensen PHB. Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms’ tumour versus normal kidney. Hum Mol Genet. 2004. 13: 2061-74.
  39. Brooks-Wilson AR, Kaurah P, Suriano G, Leach S, Senz J, Grehan N, Butterfield YSN, Jeyes J, Schinas J, Bacani J, Kelsey M, Ferreira P, MacGillivray B, MacLeod P, Ford J, Foulkes W, Greenberg C, Gilchrist D, Hughes R, Monaghan K, Oliveira MJ, Seruca R, Caldas C, Huntsman D. Germline E-Cadherin Mutations in Hereditary Diffuse Gastric Cancer: Assessment of 42 New Families and Review of Genetic Screening Criteria. J Med Genet. 2004. 41:508-17.
  40. Marra MA, Jones SJ, Astell CR, Holt RA, Brooks-Wilson A, Butterfield YS, Khattra J, Asano JK, Barber SA, Chan SY, Cloutier A, Coughlin SM, Freeman D, Girn N, Griffith OL, Leach SR, Mayo M, McDonald H, Montgomery SB, Pandoh PK, Petrescu AS, Robertson AG, Schein JE, Siddiqui A, Smailus DE, Stott JM, Yang GS, Plummer F, Andonov A, Artsob H, Bastien N, Bernard K, Booth TF, Bowness D, Czub M, Drebot M, Fernando L, Flick R, Garbutt M, Gray M, Grolla A, Jones S, Feldmann H, Meyers A, Kabani A, Li Y, Normand S, Stroher U, Tipples GA, Tyler S, Vogrig R, Ward D, Watson B, Brunham RC, Krajden M, Petric M, Skowronski DM, Upton C, Roper RL. 2003 The Genome sequence of the SARS-associated coronavirus. Science 300: 1399-404.
  41. Attie AD, Hamon Y, Brooks-Wilson AR, Gray-Keller MP, MacDonald ML, Rigot V, Tebon A, Zhang LH, Mulligan JD, Singaraja RR, Bitgood JJ, Cook ME, Kastelein JJ, Chimini G, Hayden MR. Identification and functional analysis of a naturally occurring E89K mutation in the ABCA1 gene of the WHAM chicken. J. Lipid Res. 2002; 43:1610-7.
  42. van Dam MJ, de Groot E, Clee SM, Hovingh GK, Roelants R, Brooks-Wilson A, Zwinderman AH, Smit AJ, Smelt AH, Groen AK, Hayden MR, Kastelein JJ. Association between increased arterial-wall thickness and impairment in ABCA1-driven cholesterol efflux: an observational study. Lancet 2002; 359:37-42.
  43. Lu K, Lee MH, Hazard S, Brooks-Wilson A, Hidaka H, Kojima H, Ose L, Stalenhoef AFH, Mietinnen T, Bjorkhem I, Bruckert E, Pandya A, Jr. Brewer HB, Salen G, Dean M, Patel SB. Two genes that map to the STSL locus cause sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and sterolin-2 encoded by ABCG5 and ABCG8 respectively. American Journal of Human Genetics 2001; 69:278-290.
  44. Singaraja RR, Bocher V, James ER, Clee SM, Zhang LH, Leavitt BR, Tan B, Brooks-Wilson A, Kwok A, Bissada N, Yang Y, Liu G, Tafuri SR, Fievet C, Wellington CL, Staels B, Hayden MR. Human ABCA1 BAC transgenic mice show increased HDL-C and ApoAI dependant efflux stimulated by an internal promoter containing LXREs in intron 1. J. Biol. Chem. 2001; 276:33969-33979.
  45. Clee SM, Zwinderman AH, Engert JC, Zwarts KY, Molhuizen HO, Roomp K, Jukema JW, van Wijland M, van Dam M, Hudson TJ, Brooks-Wilson A, Jr. Genest J, Kastelein JJ, Hayden MR. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease. Circulation 2001; 103:1198-205.
  46. Clee SM, Kastelein JJ, van Dam M, Marcil M, Roomp K, Zwarts KY, Collins JA, Roelants R, Tamasawa M, Stule T, Suda T, Ceska R, Boucher B, Rondeau C, DuSouich C, Brooks-Wilson A, Molhuizen HO, Frohlich J, Jr. Genest J, Hayden MR. Age and Residual Cholesterol Efflux Affect HDL Cholesterol Levels and Coronary Artery Disease in ABCA1 Heterozygotes. J. Clin. Invest. 2000; 106:1205-7.
  47. Marcil M, Brooks-Wilson A, Clee SM, Roomp K, Zhang L-H, Yu L, Collins JA, van Dam M, Molhuizen HOF, Loubster O, Ouellette BFF, Sensen CW, Fichter K, Mott S, Denis M, Boucher B, Pimstone S, Jr. Genest J, Kastelein JJ, Hayden MR. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. Lancet 1999; 354:1341-46.
  48. Brooks-Wilson A, Marcil M, Clee SM, Zhang L-H, Roomp K, van Dam M, Yu L, Brewer C, Collins JA, Molhuizen HOF, Loubster O, Ouellette BFF, Fichter K, Ashbourne-Excoffon KJD, Sensen CW, Scherer S, Mott S, Denis M, Martindale D, Frohlich J, Morgan K, Koop B, Pimstone S, Kastelein JJ, Jr. Genest J, Hayden MR. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nature Genetics 1999; 22:336-345.
  49. Brooks-Wilson AR, Emond MJ, Jr. Monnat RJ. Unexpectedly low loss of heterozygosity in genetically unstable Werner syndrome cell lines. Genes, Chromosomes and Cancer, 1997; 18:133-142.
  50. Brooks-Wilson AR, Lichter JB, Ward DC, Kidd KK, Goodfellow PJ. Genomic and yeast artificial chromosome long-range physical maps linking six loci in 10q11.2 and spanning the multiple endocrine neoplasia type 2A (MEN2A) region. Genomics, 1993; 17:611-617.
  51. Lichter JB, Wu J, Brooks-Wilson AR, Difillipantonio M, Brewster S, Ward DC, Goodfellow PJ, Kidd KK. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus. Human Genet, 1993; 90:516-20.
  52. Brooks-Wilson AR, Smailus D, Gilchrist D, Goodfellow PJ. Additional RFLPs at D10S94 and the development of PCR based variant detection systems: Implications for disease genotype prediction in MEN 2A, MEN 2B and MTC1 families. Genomics, 1992; 13:233-234.
  53. Brooks-Wilson AR, Smailus DE, Goodfellow PJ. A Cluster of CpG islands at D10S94, near the locus responsible for multiple endocrine neoplasia type 2A (MEN2A). Genomics, 1992; 13:339-343.
  54. Brooks-Wilson AR, Smailus DE, Weier HUG, Goodfellow PJ. Human Repeat Element-Mediated PCR: Cloning and Mapping of Chromosome 10 DNA Markers. Genomics, 1992; 13:409-414.
  55. Bernard LE, Brooks-Wilson AR, Wood S. Isolation of DNA Fragments from A Human Chromosomal Subregion by Alu PCR Differential Hybridization. Genomics, 1991; 9:241-246.
  56. Brooks-Wilson AR, Goodfellow PN, Povey S, Nevanlinna HA, de Jong PJ, Goodfellow PJ. Rapid Cloning and Characterization of New Chromosome 10 DNA Markers by Alu Element-Mediated PCR. Genomics, 1990; 7:614-620.
  57. Goodfellow PJ, Myers S, Anderson LL, Brooks-Wilson AR, Simpson NE. A New DNA Marker (D10S94) Very Tightly Linked to the Multiple Endocrine Neoplasia Type 2A Locus (MEN2A). Am. J. Hum. Genet, 1990; 47:952-956.
  58. Brooks-Wilson AR, Smailus D, Myers S, Anderson L, Simpson NE, Goodfellow PJ. Two polymorphisms at the D10S94 locus. Nucleic Acids Res., 1990; 18:4959.
  59. Goodfellow PJ, Brooks-Wilson AR, Smailus D, Myers S, Anderson L, Simpson NE. Three polymorphisms at the D10S85 locus. Nucleic Acids Res., 1990; 18:4960.

    60. Brooks-Wilson AR, Ball E, Pawson T. The Myristylation Signal of p60v-src Functionally Complements the N-Terminal fps-Specific Region of P130gag-fps. Mol. Cell Biol., 1989; 9:2214-2219.

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