Torthaí cuardaigh - Jonathan L. Haines
- 1 - 20 toradh as 226 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group de réir Jonathan L. Haines
Foilsithe / Cruthaithe 1998Artigo -
2
Prolonged Signal-Averaged P-Wave Duration as an Intermediate Phenotype for Familial Atrial Fibrillation de réir Dawood Darbar, Amanda Hardy, Jonathan L. Haines, Dan M. Roden
Foilsithe / Cruthaithe 2008Artigo -
3
Automated extraction of clinical traits of multiple sclerosis in electronic medical records de réir Mary F. Davis, Subramaniam Sriram, William S. Bush, Joshua C. Denny, Jonathan L. Haines
Foilsithe / Cruthaithe 2013Artigo -
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Endothelial Nitric Oxide Synthase Gene Variants and Primary Open-Angle Glaucoma de réir Jae H. Kang, Janey L. Wiggs, Bernard Rosner, Jonathan L. Haines, Wael Abdrabou, Louis R. Pasquale
Foilsithe / Cruthaithe 2011Artigo -
6
<i>LOXL1</i>Promoter Haplotypes Are Associated with Exfoliation Syndrome in a U.S. Caucasian Population de réir Bao Jian Fan, Louis R. Pasquale, Douglas J. Rhee, Tiansen Li, Jonathan L. Haines, Janey L. Wiggs
Foilsithe / Cruthaithe 2011Artigo -
7
Neurofibromatosis 2: Clinical and DNA Linkage Studies of a Large Kindred de réir Wladimir Wertelecki, Guy A. Rouleau, Duane Superneau, Lois W. Forehand, J. P. Williams, Jonathan L. Haines, James F. Gusella
Foilsithe / Cruthaithe 1988Artigo -
8
Advances in the genomics of common eye diseases de réir Jessica N. Cooke Bailey, Lucia Sobrin, Margaret A. Pericak‐Vance, Jonathan L. Haines, Christopher J. Hammond, Janey L. Wiggs
Foilsithe / Cruthaithe 2013Revisão -
9
Cardiac Sodium Channel ( <i>SCN5A</i> ) Variants Associated with Atrial Fibrillation de réir Dawood Darbar, Prince J. Kannankeril, Brian S. Donahue, Gayle Kucera, Tanya Stubblefield, Jonathan L. Haines, Alfred L. George, Dan M. Roden
Foilsithe / Cruthaithe 2008Artigo -
10
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Genetic analysis of biological pathway data through genomic randomization de réir Brian L. Yaspan, William S. Bush, Eric S. Torstenson, Deqiong Ma, Margaret A. Pericak‐Vance, Marylyn D. Ritchie, James S. Sutcliffe, Jonathan L. Haines
Foilsithe / Cruthaithe 2011Artigo -
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Novel Mutations Detected in the TSC2 Hene From Both Sporadic and Familial TSC Patients de réir Peter J. Wilson, Vijaya Ramesh, Arthur G. Kristiansen, Catherine Bove, Sergiusz Jóźwiak, David J. Kwiatkowski, M. Priscilla Short, Jonathan L. Haines
Foilsithe / Cruthaithe 1996Artigo -
14
Genome‐wide association studies identify novel loci in rapidly progressive Alzheimer's disease de réir Ping Wang, Audrey Lynn, Kristy Miskimen, Yeunjoo E. Song, Thomas Wısnıewskı, Mark L. Cohen, Brian S. Appleby, Jiri Safar, Jonathan L. Haines
Foilsithe / Cruthaithe 2024Artigo -
15
A Genomewide Scan Identifies Novel Early-Onset Primary Open-Angle Glaucoma Loci on 9q22 and 20p12 de réir J.L. Wiggs, Sally Ann Lynch, G. Ynagi, Mara Maselli, J. Auguste, Elizabeth A. Del Bono, Lana M. Olson, Jonathan L. Haines
Foilsithe / Cruthaithe 2004Artigo -
16
Endothelial Nitric Oxide Synthase Gene Variants and Primary Open-Angle Glaucoma: Interactions with Sex and Postmenopausal Hormone Use de réir Jae H. Kang, Janey L. Wiggs, Bernard Rosner, Susan E. Hankinson, Wael Abdrabou, Bao Jian Fan, Jonathan L. Haines, Louis R. Pasquale
Foilsithe / Cruthaithe 2010Artigo -
17
Genome-wide Association Study Implicates a Chromosome 12 Risk Locus for Late-Onset Alzheimer Disease de réir Gary W. Beecham, Eden R. Martin, Yi‐Ju Li, Michael A. Slifer, John R. Gilbert, Jonathan L. Haines, Margaret A. Pericak‐Vance
Foilsithe / Cruthaithe 2009Artigo -
18
Neonatal Pulmonary Hypertension de réir DeLinda L. Pearson, Sheila Dawling, William F. Walsh, Jonathan L. Haines, Brian W. Christman, Amy Bazyk, Nathan R. Scott, Marshall Summar
Foilsithe / Cruthaithe 2001Artigo -
19
Risk Factors for Progression of Age-Related Macular Degeneration: Population-Based Amish Eye Study de réir Muneeswar Gupta Nittala, Federico Corvi, Jyotsna Maram, Swetha Bindu Velaga, Jonathan L. Haines, Margaret A. Pericak‐Vance, Dwight Stambolian, Srinivas R. Sadda
Foilsithe / Cruthaithe 2022Artigo -
20
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates de réir Jacob L. McCauley, Chun Li, Lan Jiang, Lana M. Olson, Genea Crockett, Kimberly Gainer, Susan E. Folstein, Jonathan L. Haines, James S. Sutcliffe
Foilsithe / Cruthaithe 2005Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Internal medicine
Genome-wide association study
Disease
Genetic association
Allele
Neuroscience
Alzheimer's disease
Ophthalmology
Locus (genetics)
Glaucoma
Pathology
Phenotype
Computational biology
Genome
Odds ratio
Population
SNP
Open angle glaucoma
Apolipoprotein E
Environmental health
Psychology
Candidate gene
Haplotype
Mutation