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Connection

Kevin Brown to Humans

This is a "connection" page, showing publications Kevin Brown has written about Humans.
Connection Strength

1.185
  1. A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR. Am J Hum Genet. 2021 09 02; 108(9):1611-1630.
    View in: PubMed
    Score: 0.043
  2. Cell-type-specific meQTLs extend melanoma GWAS annotation beyond eQTLs and inform melanocyte gene-regulatory mechanisms. Am J Hum Genet. 2021 09 02; 108(9):1631-1646.
    View in: PubMed
    Score: 0.043
  3. Novel MAPK/AKT-impairing germline NRAS variant identified in a melanoma-prone family. Fam Cancer. 2022 07; 21(3):347-355.
    View in: PubMed
    Score: 0.043
  4. Cancer regulatory variation. Curr Opin Genet Dev. 2021 02; 66:41-49.
    View in: PubMed
    Score: 0.042
  5. Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma. Nat Commun. 2020 06 01; 11(1):2718.
    View in: PubMed
    Score: 0.040
  6. Advancements in Composite Resin Material Enable Streamlined Direct Restoration Process. Compend Contin Educ Dent. 2019 Nov/Dec; 40(suppl 2):2-6.
    View in: PubMed
    Score: 0.038
  7. A Dynamic Cis-Regulation Pattern Underlying Epithelial Ovarian Cancer Susceptibility. Cancer Res. 2019 02 01; 79(3):439-440.
    View in: PubMed
    Score: 0.036
  8. Essential cGMP Signaling in Toxoplasma Is Initiated by a Hybrid P-Type ATPase-Guanylate Cyclase. Cell Host Microbe. 2018 12 12; 24(6):804-816.e6.
    View in: PubMed
    Score: 0.036
  9. Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes. Genome Res. 2018 11; 28(11):1621-1635.
    View in: PubMed
    Score: 0.036
  10. A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF. Nat Genet. 2017 Sep; 49(9):1326-1335.
    View in: PubMed
    Score: 0.033
  11. Plasma Membrane Association by N-Acylation Governs PKG Function in Toxoplasma gondii. mBio. 2017 05 02; 8(3).
    View in: PubMed
    Score: 0.032
  12. SDHD Promoter Mutations Ablate GABP Transcription Factor Binding in Melanoma. Cancer Res. 2017 04 01; 77(7):1649-1661.
    View in: PubMed
    Score: 0.032
  13. Serum Albumin Stimulates Protein Kinase G-dependent Microneme Secretion in Toxoplasma gondii. J Biol Chem. 2016 Apr 29; 291(18):9554-65.
    View in: PubMed
    Score: 0.030
  14. A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma. Pigment Cell Melanoma Res. 2012 Nov; 25(6):815-8.
    View in: PubMed
    Score: 0.024
  15. A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature. 2011 Nov 13; 480(7375):99-103.
    View in: PubMed
    Score: 0.022
  16. Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. Nat Genet. 2009 Aug; 41(8):873-5.
    View in: PubMed
    Score: 0.019
  17. Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet. 2008 Jul; 40(7):838-40.
    View in: PubMed
    Score: 0.017
  18. Developmental expression of Toll-like receptors-2 and -4 in preterm baboon lung. Dev Comp Immunol. 2008; 32(9):1088-98.
    View in: PubMed
    Score: 0.017
  19. Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions. Nat Genet. 2024 May; 56(5):809-818.
    View in: PubMed
    Score: 0.013
  20. Qualitative research in a cross-cultural context: Fijian experiences. Qual Health Res. 2003 Mar; 13(3):333-42.
    View in: PubMed
    Score: 0.012
  21. Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity. Am J Hum Genet. 2022 Dec 01; 109(12):2210-2229.
    View in: PubMed
    Score: 0.012
  22. Rare germline deleterious variants increase susceptibility for lung cancer. Hum Mol Genet. 2022 Oct 10; 31(20):3558-3565.
    View in: PubMed
    Score: 0.012
  23. Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Hum Mol Genet. 2022 08 25; 31(17):2845-2856.
    View in: PubMed
    Score: 0.012
  24. Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation of OBFC1. Hum Mol Genet. 2022 03 21; 31(6):863-874.
    View in: PubMed
    Score: 0.011
  25. Integrated Analysis of Coexpression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. J Invest Dermatol. 2022 09; 142(9):2464-2475.e5.
    View in: PubMed
    Score: 0.011
  26. A large Canadian cohort provides insights into the genetic architecture of human hair colour. Commun Biol. 2021 11 04; 4(1):1253.
    View in: PubMed
    Score: 0.011
  27. Prospective, Multicenter, Controlled Trial of Mobile Stroke Units. N Engl J Med. 2021 09 09; 385(11):971-981.
    View in: PubMed
    Score: 0.011
  28. Genomic and evolutionary classification of lung cancer in never smokers. Nat Genet. 2021 09; 53(9):1348-1359.
    View in: PubMed
    Score: 0.011
  29. Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus. Am J Hum Genet. 2021 09 02; 108(9):1590-1610.
    View in: PubMed
    Score: 0.011
  30. Developing youth capacity for community-based research: the Sarasota County demonstration project. J Public Health Manag Pract. 2001 Mar; 7(2):53-60.
    View in: PubMed
    Score: 0.011
  31. Youth and tattoos: what school health personnel should know. J Sch Health. 2000 Nov; 70(9):355-60.
    View in: PubMed
    Score: 0.010
  32. The genomic and epigenomic evolutionary history of papillary renal cell carcinomas. Nat Commun. 2020 06 18; 11(1):3096.
    View in: PubMed
    Score: 0.010
  33. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nat Genet. 2020 05; 52(5):494-504.
    View in: PubMed
    Score: 0.010
  34. Analysis of DNA methylation patterns in the tumor immune microenvironment of metastatic melanoma. Mol Oncol. 2020 05; 14(5):933-950.
    View in: PubMed
    Score: 0.010
  35. Overlapping genetic architecture between Parkinson disease and melanoma. Acta Neuropathol. 2020 02; 139(2):347-364.
    View in: PubMed
    Score: 0.010
  36. Genetic Heterogeneity of BRAF Fusion Kinases in Melanoma Affects Drug Responses. Cell Rep. 2019 10 15; 29(3):573-588.e7.
    View in: PubMed
    Score: 0.010
  37. Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma. Melanoma Res. 2019 10; 29(5):483-490.
    View in: PubMed
    Score: 0.010
  38. Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. BMC Genet. 2019 07 17; 20(1):59.
    View in: PubMed
    Score: 0.009
  39. Sex specific associations in genome wide association analysis of renal cell carcinoma. Eur J Hum Genet. 2019 10; 27(10):1589-1598.
    View in: PubMed
    Score: 0.009
  40. The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study. PLoS Med. 2019 01; 16(1):e1002724.
    View in: PubMed
    Score: 0.009
  41. Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma. Hum Mol Genet. 2018 12 01; 27(23):4145-4156.
    View in: PubMed
    Score: 0.009
  42. Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies. J Invest Dermatol. 2018 12; 138(12):2617-2624.
    View in: PubMed
    Score: 0.009
  43. Analysis of NRAS gain in 657 patients with melanoma and evaluation of its sensitivity to a MEK inhibitor. Eur J Cancer. 2018 01; 89:90-101.
    View in: PubMed
    Score: 0.008
  44. Loci associated with skin pigmentation identified in African populations. Science. 2017 11 17; 358(6365).
    View in: PubMed
    Score: 0.008
  45. Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma. Eur Urol. 2017 11; 72(5):747-754.
    View in: PubMed
    Score: 0.008
  46. Characterising cis-regulatory variation in the transcriptome of histologically normal and tumour-derived pancreatic tissues. Gut. 2018 03; 67(3):521-533.
    View in: PubMed
    Score: 0.008
  47. Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Nat Commun. 2017 06 09; 8:15724.
    View in: PubMed
    Score: 0.008
  48. Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. Nat Commun. 2017 05 02; 8:15034.
    View in: PubMed
    Score: 0.008
  49. A melanin-bleaching methodology for molecular and histopathological analysis of formalin-fixed paraffin-embedded tissue. Lab Invest. 2016 10; 96(10):1116-27.
    View in: PubMed
    Score: 0.008
  50. A Transcriptionally Inactive ATF2 Variant Drives Melanomagenesis. Cell Rep. 2016 05 31; 15(9):1884-92.
    View in: PubMed
    Score: 0.008
  51. The genomic landscape of cutaneous melanoma. Pigment Cell Melanoma Res. 2016 May; 29(3):266-83.
    View in: PubMed
    Score: 0.007
  52. An interaction proteomics survey of transcription factor binding at recurrent TERT promoter mutations. Proteomics. 2016 Feb; 16(3):417-26.
    View in: PubMed
    Score: 0.007
  53. Germline TERT promoter mutations are rare in familial melanoma. Fam Cancer. 2016 Jan; 15(1):139-44.
    View in: PubMed
    Score: 0.007
  54. SBI-0640756 Attenuates the Growth of Clinically Unresponsive Melanomas by Disrupting the eIF4F Translation Initiation Complex. Cancer Res. 2015 Dec 15; 75(24):5211-8.
    View in: PubMed
    Score: 0.007
  55. Computational and human observer image quality evaluation of low dose, knowledge-based CT iterative reconstruction. Med Phys. 2015 Oct; 42(10):6098-111.
    View in: PubMed
    Score: 0.007
  56. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nat Genet. 2015 Sep; 47(9):987-995.
    View in: PubMed
    Score: 0.007
  57. Downregulation of the Ubiquitin Ligase RNF125 Underlies Resistance of Melanoma Cells to BRAF Inhibitors via JAK1 Deregulation. Cell Rep. 2015 Jun 09; 11(9):1458-73.
    View in: PubMed
    Score: 0.007
  58. Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. J Natl Cancer Inst. 2015 Feb; 107(2).
    View in: PubMed
    Score: 0.007
  59. A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma. Clin Genet. 2015 Sep; 88(3):267-72.
    View in: PubMed
    Score: 0.007
  60. The effect on melanoma risk of genes previously associated with telomere length. J Natl Cancer Inst. 2014 Oct; 106(10).
    View in: PubMed
    Score: 0.007
  61. Peptidyl arginine deiminase-4 activation exacerbates kidney ischemia-reperfusion injury. Am J Physiol Renal Physiol. 2014 Nov 01; 307(9):F1052-62.
    View in: PubMed
    Score: 0.007
  62. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. Int J Cancer. 2015 Mar 15; 136(6):1351-60.
    View in: PubMed
    Score: 0.007
  63. Identification of a melanoma susceptibility locus and somatic mutation in TET2. Carcinogenesis. 2014 Sep; 35(9):2097-101.
    View in: PubMed
    Score: 0.007
  64. Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One. 2014; 9(6):e100683.
    View in: PubMed
    Score: 0.007
  65. The volatile anesthetic isoflurane increases endothelial adenosine generation via microparticle ecto-5'-nucleotidase (CD73) release. PLoS One. 2014; 9(6):e99950.
    View in: PubMed
    Score: 0.007
  66. Whole genome profiling of spontaneous and chemically induced mutations in Toxoplasma gondii. BMC Genomics. 2014 May 10; 15:354.
    View in: PubMed
    Score: 0.007
  67. POT1 loss-of-function variants predispose to familial melanoma. Nat Genet. 2014 May; 46(5):478-481.
    View in: PubMed
    Score: 0.007
  68. Critical role of interleukin-11 in isoflurane-mediated protection against ischemic acute kidney injury in mice. Anesthesiology. 2013 Dec; 119(6):1389-401.
    View in: PubMed
    Score: 0.006
  69. A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers. PLoS One. 2013; 8(8):e72144.
    View in: PubMed
    Score: 0.006
  70. IL-11 is required for A1 adenosine receptor-mediated protection against ischemic AKI. J Am Soc Nephrol. 2013 Oct; 24(10):1558-70.
    View in: PubMed
    Score: 0.006
  71. A variant in FTO shows association with melanoma risk not due to BMI. Nat Genet. 2013 Apr; 45(4):428-32, 432e1.
    View in: PubMed
    Score: 0.006
  72. The volatile anesthetic isoflurane induces ecto-5'-nucleotidase (CD73) to protect against renal ischemia and reperfusion injury. Kidney Int. 2013 Jul; 84(1):90-103.
    View in: PubMed
    Score: 0.006
  73. A1 adenosine receptor allosteric enhancer PD-81723 protects against renal ischemia-reperfusion injury. Am J Physiol Renal Physiol. 2012 Sep; 303(5):F721-32.
    View in: PubMed
    Score: 0.006
  74. Array-comparative genomic hybridization reveals loss of SOCS6 is associated with poor prognosis in primary lung squamous cell carcinoma. PLoS One. 2012; 7(2):e30398.
    View in: PubMed
    Score: 0.006
  75. Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing. Nat Genet. 2011 Dec 25; 44(2):165-9.
    View in: PubMed
    Score: 0.006
  76. Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. J Invest Dermatol. 2012 Feb; 132(2):485-7.
    View in: PubMed
    Score: 0.005
  77. Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nat Genet. 2011 Oct 09; 43(11):1114-8.
    View in: PubMed
    Score: 0.005
  78. Genome-wide association study identifies three new melanoma susceptibility loci. Nat Genet. 2011 Oct 09; 43(11):1108-13.
    View in: PubMed
    Score: 0.005
  79. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Hum Mol Genet. 2011 Dec 15; 20(24):5012-23.
    View in: PubMed
    Score: 0.005
  80. A toll-like receptor-4-interacting surfactant protein-A-derived peptide suppresses tumor necrosis factor-a release from mouse JAWS II dendritic cells. J Pharmacol Exp Ther. 2011 Mar; 336(3):672-81.
    View in: PubMed
    Score: 0.005
  81. Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Nat Genet. 2010 Aug; 42(8):661-4.
    View in: PubMed
    Score: 0.005
  82. A versatile gene-based test for genome-wide association studies. Am J Hum Genet. 2010 Jul 09; 87(1):139-45.
    View in: PubMed
    Score: 0.005
  83. Toxoplasma gondii activates hypoxia-inducible factor (HIF) by stabilizing the HIF-1alpha subunit via type I activin-like receptor kinase receptor signaling. J Biol Chem. 2010 Aug 27; 285(35):26852-26860.
    View in: PubMed
    Score: 0.005
  84. Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies. PLoS One. 2010 May 28; 5(5):e10858.
    View in: PubMed
    Score: 0.005
  85. Protection against acute kidney injury via A(1) adenosine receptor-mediated Akt activation reduces liver injury after liver ischemia and reperfusion in mice. J Pharmacol Exp Ther. 2010 Jun; 333(3):736-47.
    View in: PubMed
    Score: 0.005
  86. Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet. 2009 Aug; 41(8):920-5.
    View in: PubMed
    Score: 0.005
  87. Human heat shock protein 27 overexpressing mice are protected against hepatic ischemia and reperfusion injury. Transplantation. 2009 May 27; 87(10):1478-87.
    View in: PubMed
    Score: 0.005
  88. Should all patients with duodenal adenocarcinoma be considered for aggressive surgical resection? Am J Surg. 2007 Mar; 193(3):319-24; discussion 324-5.
    View in: PubMed
    Score: 0.004
  89. Quantitation of heteroplasmy of mtDNA sequence variants identified in a population of AD patients and controls by array-based resequencing. Mitochondrion. 2006 Aug; 6(4):194-210.
    View in: PubMed
    Score: 0.004
  90. Epigenetic transdifferentiation of normal melanocytes by a metastatic melanoma microenvironment. Cancer Res. 2005 Nov 15; 65(22):10164-9.
    View in: PubMed
    Score: 0.004
  91. Gene expression correlates of neurofibrillary tangles in Alzheimer's disease. Neurobiol Aging. 2006 Oct; 27(10):1359-71.
    View in: PubMed
    Score: 0.004
  92. An expression signature classifies chemotherapy-resistant pediatric osteosarcoma. Cancer Res. 2005 Mar 01; 65(5):1748-54.
    View in: PubMed
    Score: 0.003
  93. Sarcoidosis: social predictors of severity at presentation. Eur Respir J. 2004 Oct; 24(4):601-8.
    View in: PubMed
    Score: 0.003
  94. Inter-platform comparability of microarrays in acute lymphoblastic leukemia. BMC Genomics. 2004 Sep 23; 5:71.
    View in: PubMed
    Score: 0.003
  95. The use of gene expression analysis to gain insights into signaling mechanisms of metastatic medulloblastoma. Pediatr Neurosurg. 2003 Jul; 39(2):68-74.
    View in: PubMed
    Score: 0.003
  96. Overexpression of the EGFR/FKBP12/HIF-2alpha pathway identified in childhood astrocytomas by angiogenesis gene profiling. Cancer Res. 2003 Apr 15; 63(8):1865-70.
    View in: PubMed
    Score: 0.003
  97. Occurrence of NKX3.1 C154T polymorphism in men with and without prostate cancer and studies of its effect on protein function. Cancer Res. 2002 May 01; 62(9):2654-9.
    View in: PubMed
    Score: 0.003
  98. Variation in the ESR1 and ESR2 genes and genetic susceptibility to anorexia nervosa. Mol Psychiatry. 2002; 7(1):86-9.
    View in: PubMed
    Score: 0.003
  99. No missense mutation of WKL1 in a subgroup of probands with schizophrenia. Mol Psychiatry. 2002; 7(4):419-23.
    View in: PubMed
    Score: 0.003
  100. Severe autosomal recessive rippling muscle disease. Muscle Nerve. 2001 Nov; 24(11):1542-7.
    View in: PubMed
    Score: 0.003
  101. Expression profiling of medulloblastoma: PDGFRA and the RAS/MAPK pathway as therapeutic targets for metastatic disease. Nat Genet. 2001 Oct; 29(2):143-52.
    View in: PubMed
    Score: 0.003
  102. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation. 2001 Jan 30; 103(4):485-90.
    View in: PubMed
    Score: 0.003
  103. A cholesterol-lowering diet does not produce adverse psychological effects in children: three-year results from the dietary intervention study in children. Health Psychol. 1999 Nov; 18(6):604-13.
    View in: PubMed
    Score: 0.002
  104. Epithelin/granulin growth factors: extracellular cofactors for HIV-1 and HIV-2 Tat proteins. Biochem Biophys Res Commun. 1999 Mar 16; 256(2):299-306.
    View in: PubMed
    Score: 0.002
  105. Maternal acceptability of a dietary intervention designed to lower children's intake of saturated fat and cholesterol: the Dietary Intervention Study in Children (DISC). J Am Diet Assoc. 1998 Jan; 98(1):31-4.
    View in: PubMed
    Score: 0.002
  106. Automated detection of prevalent mutations in BRCA1 and BRCA2 genes, using a fluorogenic PCR allelic discrimination assay. Genet Test. 1997-1998; 1(3):171-80.
    View in: PubMed
    Score: 0.002
  107. A 36-kilodalton cellular transcription factor mediates an indirect interaction of human T-cell leukemia/lymphoma virus type I TAX1 with a responsive element in the viral long terminal repeat. Mol Cell Biol. 1990 Aug; 10(8):4192-201.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.

THIS IS A DEVELOPMENT VERSION OF PROFILES. PLEASE GO TO THE PRODUCTION ENVIRONMENT FOR UPDATES