Works by Lathrop, G. Mark
Results: 36
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.
- Published in:
- Nature, 1988, v. 336, n. 6199, p. 577, doi. 10.1038/336577a0
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- Publication type:
- Article
SNP haplotype tagging from DNA pools of two individuals.
- Published in:
- BMC Bioinformatics, 2003, v. 4, p. 14, doi. 10.1186/1471-2105-4-14
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- Publication type:
- Article
Aristolochic acid exposure in Romania and implications for renal cell carcinoma.
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- 2016
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- Publication type:
- journal article
An epigenome-wide association study of total serum immunoglobulin E concentration.
- Published in:
- Nature, 2015, v. 520, n. 7549, p. 670, doi. 10.1038/nature14125
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- Publication type:
- Article
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 8, p. 1365, doi. 10.1093/hmg/ddl058
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- Publication type:
- Article
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
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- Human Molecular Genetics, 2005, v. 14, n. 13, p. 1805, doi. 10.1093/hmg/ddi187
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- Publication type:
- Article
Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome.
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- Human Molecular Genetics, 2004, v. 13, n. 15, p. 1623, doi. 10.1093/hmg/ddh177
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- Publication type:
- Article
Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides.
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- Human Molecular Genetics, 2002, v. 11, n. 23, p. 2969, doi. 10.1093/hmg/11.23.2969
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- Publication type:
- Article
Genomic analysis defines distinct pancreatic and neuronal subtypes of lung carcinoid.
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- Journal of Pathology, 2024, v. 264, n. 3, p. 332, doi. 10.1002/path.6352
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- Publication type:
- Article
Wolcott-Rallison Syndrome.
- Published in:
- Diabetes, 2004, v. 53, n. 7, p. 1876, doi. 10.2337/diabetes.53.7.1876
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- Publication type:
- Article
A comparison of two algorithms, multimap and gene mapping system, for automated construction of genetic linkage maps.
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- Genetic Epidemiology, 1999, v. 17, p. S649, doi. 10.1002/gepi.13701707106
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- Publication type:
- Article
eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissues.
- Published in:
- Nature Communications, 2015, v. 6, n. 5, p. 6821, doi. 10.1038/ncomms7821
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- Publication type:
- Article
Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus.
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- Annals of Human Genetics, 2013, v. 77, n. 6, p. 465, doi. 10.1111/ahg.12034
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- Publication type:
- Article
Fine mapping of eight psoriasis susceptibility loci.
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- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 844, doi. 10.1038/ejhg.2014.172
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- Publication type:
- Article
SLC2A9 Is a High-Capacity Urate Transporter in Humans.
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- PLoS Medicine, 2008, v. 5, n. 10, p. 1509, doi. 10.1371/journal.pmed.0050197
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- Publication type:
- Article
Genetic and Haplotypic Structure in 14 European and Mrican Cattle Breeds.
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- Genetics, 2007, v. 177, n. 2, p. 1059, doi. 10.1534/genetics.107.075804
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- Publication type:
- Article
Rat Gene Mapping Using PCR-Analyzed Microsatellites.
- Published in:
- Genetics, 1992, v. 131, n. 3, p. 701
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- Publication type:
- Article
Association of ulcerative colitis with rare VNTR alleles of the human intestinal mucin gene, MUC3.
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- Human Molecular Genetics, 1999, v. 8, n. 2, p. 307, doi. 10.1093/hmg/8.2.307
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- Publication type:
- Article
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2077, doi. 10.1093/hmg/6.12.2077
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- Publication type:
- Article
Identification of a Major Susceptibility Locus on Chromosome 6p and Evidence for Further Disease Loci Revealed by a Two Stage Genome-Wide Search in Psoriasis.
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- Human Molecular Genetics, 1997, v. 6, n. 5, p. 813, doi. 10.1093/hmg/6.5.813
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- Publication type:
- Article
Location of the First Genetic Locus, PKDr1, Controlling Autosomal Dominant Polycystic Kidney Disease in Han:SPRD cy/+ rat.
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- Human Molecular Genetics, 1997, v. 6, n. 4, p. 609, doi. 10.1093/hmg/6.4.609
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- Publication type:
- Article
Identification of Nine Novel Mutations in the Hepatocyte Nuclear Factor 1 Alpha Aene Associated with Maturity-Onset Diabetes of the Young (MODY3).
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- Human Molecular Genetics, 1997, v. 6, n. 4, p. 583, doi. 10.1093/hmg/6.4.583
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- Publication type:
- Article
EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome.
- Published in:
- Nature Genetics, 2000, v. 25, n. 4, p. 406, doi. 10.1038/78085
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- Publication type:
- Article
Fine-mapping of an ancestral recombination breakpoint in DCP1.
- Published in:
- Nature Genetics, 1999, v. 23, n. 3, p. 270, doi. 10.1038/15449
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- Publication type:
- Article
Mutations in ATP2A2, encoding a Ca<sup>2+</sup> pump, cause Darier disease.
- Published in:
- Nature Genetics, 1999, v. 21, n. 3, p. 271, doi. 10.1038/6784
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- Publication type:
- Article
Goodness-of-fit tests for locus order in three-point mapping.
- Published in:
- Genetic Epidemiology, 1987, v. 4, n. 1, p. 51, doi. 10.1002/gepi.1370040107
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- Publication type:
- Article
Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees.
- Published in:
- Human Heredity, 2011, v. 71, n. 2, p. 126, doi. 10.1159/000324177
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- Publication type:
- Article
Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.
- Published in:
- Clinical Genetics, 1989, v. 36, n. 6, p. 459, doi. 10.1111/j.1399-0004.1989.tb03377.x
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- Publication type:
- Article
High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity.
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- European Journal of Human Genetics, 2002, v. 10, n. 9, p. 553, doi. 10.1038/sj.ejhg.5200847
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- Publication type:
- Article
A genome-wide association study of global gene expression.
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- Nature Genetics, 2007, v. 39, n. 10, p. 1202, doi. 10.1038/ng2109
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- Publication type:
- Article
A variant in the CD209 promoter is associated with severity of dengue disease.
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- Nature Genetics, 2005, v. 37, n. 5, p. 507, doi. 10.1038/ng1550
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- Article
Duplicating SNPs.
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- Nature Genetics, 2004, v. 36, n. 8, p. 789, doi. 10.1038/ng0804-789
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- Article
Characterization of newly developed SSLP markers for the rat.
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- Mammalian Genome, 2000, v. 11, n. 4, p. 300, doi. 10.1007/s003350010056
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- Article
Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells.
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- BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0220-7
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- Publication type:
- Article
Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11.
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- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013750
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- Publication type:
- Article
Polymorphisms in the WNK1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion.
- Published in:
- PLoS ONE, 2009, v. 4, n. 4, p. 1, doi. 10.1371/journal.pone.0005003
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- Publication type:
- Article