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Articles in Scholarly Journals [Incomplete List]

1. Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: The Cardiovascular Health Study
   Atherosclerosis, vol. 197, no. 2, pp. 922–930, 2008
2. Common ß-adrenergic receptor polymorphisms are not associated with risk of sudden cardiac death in patients with coronary artery disease
   Heart Rhythm, vol. 5, no. 6, pp. 814–821, 2008
3. Differences in allergic sensitization by self-reported race and genetic ancestry
   Journal of Allergy and Clinical Immunology, vol. 122, no. 4, pp. 820–827.e9, 2008
4. Natural variation in four human collagen genes across an ethnically diverse population
   Genomics, vol. 91, no. 4, pp. 307–314, 2008
5. Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus
   Nature Genetics, vol. 40, no. 9, Article ID ng.202, 2 pages, 2008
6. Endothelial Nitric Oxide Synthase Polymorphism (-786T->C) and Increased Risk of Angiographic Vasospasm After Aneurysmal Subarachnoid Hemorrhage
   Stroke, vol. 39, no. 4, pp. 1103–1108, 2008
7. A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci
   PLoS Genetics, vol. 4, no. 3, p. e1000041, 2008
8. SNPs Meet CNVs in Genome-Wide Association Studies: HGV2007 Meeting Report
   PLoS Genetics, vol. 4, no. 4, p. e1000068, 2008
9. An apolipoprotein A-V gene SNP is associated with marked hypertriglyceridemia among Asian-American patients
   The Journal of Lipid Research, vol. 49, no. 8, pp. 1846–1854, 2008
10. Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis
    Nature Genetics, vol. 39, no. 2, Article ID ng0207-153, 2 pages, 2007
11. Genome-wide detection and characterization of positive selection in human populations
    Nature, vol. 449, no. 7164, Article ID nature06250, 5 pages, 2007
12. A second generation human haplotype map of over 3.1 million SNPs
    Nature, vol. 449, no. 7164, Article ID nature06258, 10 pages, 2007
13. Recommendations of the 2006 Human Variome Project meeting
    Nature Genetics, vol. 39, no. 4, Article ID ng2024, 3 pages, 2007
14. Gene-trapped mouse embryonic stem cell-derived cardiac myocytes and human genetics implicate AKAP10 in heart rhythm regulation
    Proceedings of the National Academy of Sciences, vol. 104, no. 20, pp. 8461–8466, 2007
15. Admixture Mapping of an Allele Affecting Interleukin 6 Soluble Receptor and Interleukin 6 Levels
    The American Journal of Human Genetics, vol. 80, no. 4, pp. 716–726, 2007
16. Rapid DNA mapping by fluorescent single molecule detection
    Nucleic Acids Research, vol. 35, no. 3, pp. e16–e16, 2007
17. Apolipoprotein E e4 Allele Increases the Risk of Early Postoperative Delirium in Older Patients Undergoing Noncardiac Surgery
    Anesthesiology, vol. 107, no. 3, pp. 406–411, 2007
18. Identification of NR1I2 genetic variation using resequencing
    European Journal of Clinical Pharmacology, vol. 63, no. 6, pp. 547–554, 2007
19. Determination of haplotypes from single DNA molecules: a method for single-molecule barcoding
    Human Mutation, vol. 28, no. 9, pp. 913–921, 2007
20. Distribution of human SNPs and its effect on high-throughput genotyping
    Human Mutation, vol. 27, no. 3, pp. 249–254, 2006
21. Seventh international meeting on single nucleotide polymorphism and complex genome analysis: ‘ever bigger scans and an increasingly variable genome’
    Human Genetics, vol. 119, no. 4, pp. 451–456, 2006
22. A simple DNA stretching method for fluorescence imaging of single DNA molecules
    Nucleic Acids Research, vol. 34, no. 17, pp. e113–e113, 2006
23. Apolipoprotein E ϵ2 Is Associated with New Hemorrhage Risk in Brain Arteriovenous Malformations
    Neurosurgery, vol. 58, no. 5, pp. 838–843, 2006
24. African Ancestry, Socioeconomic Status, and Kidney Function in Elderly African Americans: A Genetic Admixture Analysis
    Journal of the American Society of Nephrology, vol. 17, no. 12, pp. 3491–3496, 2006
25. Human Variome Project: an international collaboration to catalogue human genetic variation
    Pharmacogenomics, vol. 7, no. 7, pp. 969–972, 2006
26. Adrenoceptor Polymorphisms and the Risk of Cardiac Injury and Dysfunction After Subarachnoid Hemorrhage
    Stroke, vol. 37, no. 7, pp. 1680–1685, 2006
27. Response to Letter by Atanassova
    Stroke, vol. 37, no. 12, pp. 2873–2873, 2006
28. Lack of Support for the Association between GAD2 Polymorphisms and Severe Human Obesity
    PLoS Biology, vol. 3, no. 9, p. e315, 2005
29. Polymorphism discovery in 51 chemotherapy pathway genes
    Human Molecular Genetics, vol. 14, no. 23, pp. 3595–3603, 2005
30. Population Structure, Admixture, and Aging-Related Phenotypes in African American Adults: The Cardiovascular Health Study
    The American Journal of Human Genetics, vol. 76, no. 3, pp. 463–477, 2005
31. Polymorphisms in Transforming Growth Factor- -Related Genes ALK1 and ENG Are Associated With Sporadic Brain Arteriovenous Malformations
    Stroke, vol. 36, no. 10, pp. 2278–2280, 2005
32. Tumor Necrosis Factor- -238G>A Promoter Polymorphism Is Associated With Increased Risk of New Hemorrhage in the Natural Course of Patients With Brain Arteriovenous Malformations
    Stroke, vol. 37, no. 1, pp. 231–234, 2005
33. High-density single-nucleotide polymorphism maps of the human genome
    Genomics, vol. 86, no. 2, pp. 117–126, 2005
34. Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR
    Human Genetics, vol. 118, no. 3-4, pp. 466–476, 2005
35. Population stratification confounds genetic association studies among Latinos
    Human Genetics, vol. 118, no. 5, pp. 652–664, 2005
36. Interleukin-6 involvement in brain arteriovenous malformations
    Annals of Neurology, vol. 59, no. 1, pp. 72–80, 2005
37. Genetic admixture and asthma-related phenotypes in Mexican American and Puerto Rican asthmatics
    Genetic Epidemiology, vol. 29, no. 1, pp. 76–86, 2005
38. Variations in human HM74 (GPR109B) and HM74A (GPR109A) niacin receptors
    Human Mutation, vol. 25, no. 1, pp. 18–21, 2004
39. Pharmacogenomic assessment of carboxylesterases 1 and 2
    Genomics, vol. 84, no. 4, pp. 661–668, 2004
40. Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens
    Genomics, vol. 84, no. 6, pp. 899–912, 2004
41. Role of Excess Inorganic Pyrophosphate in Primer-Extension Genotyping Assays
    Genome Research, vol. 14, no. 9, pp. 1749–1755, 2004
42. High-throughput Genotyping Methods for Pharmacogenomic Studies
    Current Pharmacogenomics, vol. 2, no. 1, pp. 21–33, 2004
43. Polymorphisms in Genes Involved in Inflammatory and Angiogenic Pathways and the Risk of Hemorrhagic Presentation of Brain Arteriovenous Malformations
    Stroke, vol. 35, no. 10, pp. 2294–2300, 2004
44. ADAM33 Is Not Associated with Asthma in Puerto Rican or Mexican Populations
    American Journal of Respiratory and Critical Care Medicine, vol. 168, no. 11, pp. 1312–1316, 2003
45. Efficient High-Throughput Resequencing of Genomic DNA
    Genome Research, vol. 13, no. 4, pp. 717–720, 2003
46. DNA Analysis by Fluorescence Quenching Detection
    Genome Research, vol. 13, no. 5, pp. 932–939, 2003
47. A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis
    Nature Genetics, vol. 35, no. 4, Article ID ng1268, 7 pages, 2003
48. Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility
    Human Genetics, vol. 112, no. 1, pp. 34–41, 2003
49. Identification of a frequent variant inALG6, the cause of Congenital Disorder of Glycosylation-Ic
    Human Mutation, vol. 22, no. 5, pp. 420–421, 2003
50. Paternal Origins of Complete Hydatidiform Moles Proven by Whole Genome Single-Nucleotide Polymorphism Haplotyping
    Genomics, vol. 79, no. 1, pp. 58–62, 2002
51. SNP genotyping with fluorescence polarization detection
    Human Mutation, vol. 19, no. 4, pp. 315–323, 2002
52. SNP databases and pharmacogenetics: great start, but a long way to go
    Human Mutation, vol. 20, no. 3, pp. 174–179, 2002
53. Making 'random amplification' predictable in whole genome analysis
    Trends in Biotechnology, vol. 20, no. 10, pp. 411–412, 2002
54. Sequence variations in the public human genome data reflect a bottlenecked population history
    Proceedings of the National Academy of Sciences, vol. 100, no. 1, pp. 376–381, 2002
55. The optimal measure of allelic association
    Proceedings of the National Academy of Sciences, vol. 98, no. 9, pp. 5217–5221, 2001
56. 3rd International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis: SNPs: ‘Some Notable Progress’
    European Journal of Human Genetics, vol. 9, no. 4, Article ID 5200616, 2 pages, 2001
57. Advances in molecular medicine
    Journal of the American Academy of Dermatology, vol. 44, no. 5, pp. 847–855, 2001
58. Nature Biotechnology, vol. 19, no. 1, pp. 18–19, 2001
59. Nature Genetics, vol. 27, no. 4, pp. 371–372, 2001
60. GENOMICS: Genetic Association by Whole-Genome Analysis?
    Science, vol. 294, no. 5547, pp. 1669–1670, 2001
61. METHODS FOR GENOTYPING SINGLE NUCLEOTIDE POLYMORPHISMS
    Annual Review of Genomics and Human Genetics, vol. 2, no. 1, pp. 235–258, 2001
62. Fluorescence Polarization in Homogeneous Nucleic Acid Analysis II: 5'-Nuclease Assay
    Genome Research, vol. 11, no. 3, pp. 436–440, 2001
63. The birth and death of human single-nucleotide polymorphisms: new experimental evidence and implications for human history and medicine
    Human Molecular Genetics, vol. 10, no. 20, pp. 2195–2198, 2001
64. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
    Nature, vol. 409, no. 6822, Article ID 35057149, 5 pages, 2001
65. SNiPpets from the Third International Meeting on Single Nucleotide Polymorphism and Complex Genome Analysis, September 8-11, 2000, Taos, New Mexico, USA
    Human Mutation, vol. 17, no. 4, pp. 241–242, 2001
66. Allelic association with SNPs: Metrics, populations, and the linkage disequilibrium map
    Human Mutation, vol. 17, no. 4, pp. 255–262, 2001
67. Regions of Low Single-Nucleotide Polymorphism Incidence in Human and Orangutan Xq: Deserts and Recent Coalescences
    Genomics, vol. 71, no. 1, pp. 78–88, 2001
68. A High-Density Single-Nucleotide Polymorphism Map of Xq25–q28
    Genomics, vol. 65, no. 3, pp. 195–202, 2000
69. Linkage of a Gene for Familial Hypobetalipoproteinemia to Chromosome 3p21.1-22
    The American Journal of Human Genetics, vol. 66, no. 5, pp. 1699–1704, 2000
70. Nature Genetics, vol. 25, no. 3, pp. 324–328, 2000
71. Alternative splicing for the α1 subunit of soluble guanylate cyclase
    Biochemical Journal, vol. 346, no. 3, p. 811, 2000
72. High-throughput genotyping assay approaches
    Pharmacogenomics, vol. 1, no. 1, pp. 95–100, 2000
73. Approaches to allele frequency determination
    Pharmacogenomics, vol. 1, no. 2, pp. 231–235, 2000
74. Nature Genetics, vol. 23, no. 4, pp. 452–456, 1999
75. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes
    Human Molecular Genetics, vol. 8, no. 9, pp. 1631–1636, 1999
76. Homogeneous genotyping assays for single nucleotide polymorphisms with fluorescence resonance energy transfer detection
    Genetic Analysis: Biomolecular Engineering, vol. 14, no. 5-6, pp. 157–163, 1999
77. Single nucleotide polymorphism libraries: why and how are we building them?
    Molecular Medicine Today, vol. 5, no. 12, pp. 538–543, 1999
78. Nature Biotechnology, vol. 16, no. 13, pp. 1314–1315, 1998
79. Diabetes mellitus in a new kindred with familial hypobetalipoproteinemia and an apolipoprotein B truncation (apoB-55)
    Atherosclerosis, vol. 136, no. 2, pp. 289–295, 1998
80. Single nucleotide polymorphism hunting in cyberspace
    Human Mutation, vol. 12, no. 4, pp. 221–225, 1998
81. The Homozygous Complete Hydatidiform Mole: A Unique Resource for Genome Studies
    Genomics, vol. 46, no. 2, pp. 307–310, 1997
82. Template-directed dye-terminator incorporation (TDI) assay: a homogeneous DNA diagnostic method based on fluorescence resonance energy transfer
    Nucleic Acids Research, vol. 25, no. 2, pp. 347–353, 1997
83. Fluorescence energy transfer detection as a homogeneous DNA diagnostic method
    Proceedings of the National Academy of Sciences, vol. 94, no. 20, pp. 10756–10761, 1997
84. Increasing the Information Content of STS-Based Genome Maps: Identifying Polymorphisms in Mapped STSs
    Genomics, vol. 31, no. 1, pp. 123–126, 1996
85. Comparative Analysis of Human DNA Variations by Fluorescence-Based Sequencing of PCR Products
    Genomics, vol. 23, no. 1, pp. 138–144, 1994
86. Physical Calibration of Yeast Artificial Chromosome Contig Maps by RecA-Assisted Restriction Endonuclease (RARE) Cleavage
    Genomics, vol. 24, no. 2, pp. 199–210, 1994
87. Automatable screening of yeast artificial-chromosome libraries based on the oligonucleotide-ligation assay
    Genomics, vol. 13, no. 4, pp. 935–941, 1992