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Nicht-invasiver Pränataltest (NIPT): Aktuelle gesundheitspolitische Initiativen und inhaltliche Missverständnisse.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Persistent symptoms and risk factors predicting prolonged time to symptom-free after SARS‑CoV‑2 infection: an analysis of the baseline examination of the German COVIDOM/NAPKON-POP cohort.
- Published in:
- Infection, 2023, v. 51, n. 6, p. 1679, doi. 10.1007/s15010-023-02043-6
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- Publication type:
- Article
Heritability of chronic venous disease.
- Published in:
- Human Genetics, 2010, v. 127, n. 6, p. 669, doi. 10.1007/s00439-010-0812-9
- By:
- Publication type:
- Article
Mathew B. Hamilton: Population genetics.
- Published in:
- 2009
- By:
- Publication type:
- Book Review
A comprehensive evaluation of SNP genotype imputation.
- Published in:
- Human Genetics, 2009, v. 125, n. 2, p. 163, doi. 10.1007/s00439-008-0606-5
- By:
- Publication type:
- Article
Genetic variation at the growth hormone ( GH1) and growth hormone receptor ( GHR) loci as a risk factor for hypertension and stroke.
- Published in:
- Human Genetics, 2006, v. 119, n. 5, p. 527, doi. 10.1007/s00439-006-0166-5
- By:
- Publication type:
- Article
Signature of recent historical events in the European Y-chromosomal STR haplotype distribution.
- Published in:
- Human Genetics, 2005, v. 116, n. 4, p. 279, doi. 10.1007/s00439-004-1201-z
- By:
- Publication type:
- Article
Patterns of linkage disequilibrium in the MHC region on human chromosome 6p.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 377, doi. 10.1007/s00439-003-1075-5
- By:
- Publication type:
- Article
Entropy-based SNP selection for genetic association studies.
- Published in:
- Human Genetics, 2003, v. 114, n. 1, p. 36, doi. 10.1007/s00439-003-1017-2
- By:
- Publication type:
- Article
Three different pathological lesions in the NF1 gene originating de novo in a family with neurofibromatosis type 1.
- Published in:
- Human Genetics, 2003, v. 112, n. 1, p. 12, doi. 10.1007/s00439-002-0840-1
- By:
- Publication type:
- Article
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
- Published in:
- Human Genetics, 2002, v. 110, n. 1, p. 52, doi. 10.1007/s00439-001-0645-7
- By:
- Publication type:
- Article
ASP – a simulation-based power calculator for genetic linkage studies of qualitative traits, using sib-pairs.
- Published in:
- Human Genetics, 2001, v. 109, n. 6, p. 675, doi. 10.1007/s00439-001-0634-x
- By:
- Publication type:
- Article
Correcting for multiple testing in genetic association studies: the legend lives on.
- Published in:
- Human Genetics, 2001, v. 109, n. 5, p. 566, doi. 10.1007/s00439-001-0616-z
- By:
- Publication type:
- Article
Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaques.
- Published in:
- Human Genetics, 2001, v. 108, n. 3, p. 249, doi. 10.1007/s004390100485
- By:
- Publication type:
- Article
Human type I hair keratin pseudogene ϕhHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence.
- Published in:
- Human Genetics, 2001, v. 108, n. 1, p. 37, doi. 10.1007/s004390000439
- By:
- Publication type:
- Article
The Frequency of Inherited Disorders Database.
- Published in:
- Human Genetics, 2001, v. 108, n. 1, p. 72, doi. 10.1007/s004390000408
- By:
- Publication type:
- Article
Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions.
- Published in:
- Human Genetics, 2000, v. 107, n. 4, p. 362, doi. 10.1007/s004390000393
- By:
- Publication type:
- Article
Molecular analysis of the genotype-phenotype relationship in factor X deficiency.
- Published in:
- Human Genetics, 2000, v. 106, n. 2, p. 249, doi. 10.1007/s004390051035
- By:
- Publication type:
- Article
Paternal kin bias in the agonistic interventions of adult female rhesus macaques ( Macaca mulatta).
- Published in:
- Behavioral Ecology & Sociobiology, 2006, v. 61, n. 2, p. 205, doi. 10.1007/s00265-006-0251-8
- By:
- Publication type:
- Article
Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer.
- Published in:
- International Journal of Cancer, 2007, v. 121, n. 3, p. 555, doi. 10.1002/ijc.22735
- By:
- Publication type:
- Article
GrabBlur - a framework to facilitate the secure exchange of whole-exome and -genome SNV data using VCF files.
- Published in:
- BMC Genomics, 2014, v. 15, p. 1, doi. 10.1186/1471-2164-15-S4-S8
- By:
- Publication type:
- Article
Genetic Studies on the Cayo Santiago Rhesus Macaques: A Review of 40 Years Of Research.
- Published in:
- American Journal of Primatology, 2016, v. 78, n. 1, p. 44, doi. 10.1002/ajp.22424
- By:
- Publication type:
- Article
Comparative Assessment of the Association Information Captured by SNP Tagging.
- Published in:
- Human Heredity, 2007, v. 64, n. 1, p. 27, doi. 10.1159/000101420
- By:
- Publication type:
- Article
SNP-Based Analysis of Genetic Substructure in the German Population.
- Published in:
- Human Heredity, 2006, v. 62, n. 1, p. 20, doi. 10.1159/000095850
- By:
- Publication type:
- Article
Genetics of Crohn disease, an archetypal inflammatory barrier disease.
- Published in:
- Nature Reviews Genetics, 2005, v. 6, n. 5, p. 376, doi. 10.1038/nrg1607
- By:
- Publication type:
- Article
A novel scatterplot-based method to detect copy number variation (CNV).
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1166972
- By:
- Publication type:
- Article
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 8, p. 1660, doi. 10.1093/hmg/ddr035
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- Publication type:
- Article
Genomic and geographic distribution of SNP-defined runs of homozygosity in Europeans.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 15, p. 2927, doi. 10.1093/hmg/ddq198
- By:
- Publication type:
- Article
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 18, p. 3516, doi. 10.1093/hmg/ddp296
- By:
- Publication type:
- Article
A common haplotype of the annexin A5 (ANXA5) gene promoter is associated with recurrent pregnancy loss.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 5, p. 573, doi. 10.1093/hmg/ddm017
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- Publication type:
- Article
Transcriptomic alterations during ageing reflect the shift from cancer to degenerative diseases in the elderly.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41467-017-02395-2
- By:
- Publication type:
- Article
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
- Published in:
- BMC Medical Genetics, 2017, v. 18, n. 1, p. 1, doi. 10.1186/s12881-017-0447-y
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- Publication type:
- Article
Association of inflammatory bowel disease with indicators for childhood antigen and infection exposure.
- Published in:
- International Journal of Colorectal Disease, 2003, v. 18, n. 5, p. 413, doi. 10.1007/s00384-003-0484-1
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- Publication type:
- Article
p53 mutations, benzo[a]pyrene and lung cancer.
- Published in:
- Mutagenesis, 1998, v. 13, n. 4, p. 319, doi. 10.1093/mutage/13.4.319
- By:
- Publication type:
- Article
Empirical Evaluation Reveals Best Fit of a Logistic Mutation Model for Human Y-Chromosomal Microsatellites.
- Published in:
- Genetics, 2011, v. 189, n. 4, p. 1403, doi. 10.1534/genetics.111.132308
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- Publication type:
- Article
Population-Based Biobanking.
- Published in:
- Genes, 2024, v. 15, n. 1, p. 66, doi. 10.3390/genes15010066
- By:
- Publication type:
- Article
PanelDesign: Integrating Epidemiological Information into the Design of Diagnostic NGS Gene Panels.
- Published in:
- Genes, 2022, v. 13, n. 4, p. 684, doi. 10.3390/genes13040684
- By:
- Publication type:
- Article
Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's Disease.
- Published in:
- Genes, 2021, v. 12, n. 12, p. 1859, doi. 10.3390/genes12121859
- By:
- Publication type:
- Article
Genetic investigation of FOXO3A requires special attention due to sequence homology with FOXO3B.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 2, p. 240, doi. 10.1038/ejhg.2012.83
- By:
- Publication type:
- Article
Copy number variation in patients with cervical artery dissection.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1295, doi. 10.1038/ejhg.2012.82
- By:
- Publication type:
- Article
The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 9, p. 911, doi. 10.1038/ejhg.2012.56
- By:
- Publication type:
- Article
Legal and ethical consequences of international biobanking from a national perspective: the German BMB-EUCoop project.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 5, p. 522, doi. 10.1038/ejhg.2009.214
- By:
- Publication type:
- Article
Hypotheses in genome-wide association scans.
- Published in:
- 2008
- By:
- Publication type:
- Letter
A legal framework for biobanking: the German experience.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 5, p. 528, doi. 10.1038/sj.ejhg.5201810
- By:
- Publication type:
- Article
Y-chromosomal STR haplotype analysis reveals surname-associated strata in the East-German population.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 5, p. 577, doi. 10.1038/sj.ejhg.5201572
- By:
- Publication type:
- Article
Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 6, doi. 10.1038/sj.ejhg.5200897
- By:
- Publication type:
- Article
Adjustment for smoking does not alter the FOXO3A association with longevity.
- Published in:
- Age, 2014, v. 36, n. 2, p. 911, doi. 10.1007/s11357-013-9578-z
- By:
- Publication type:
- Article
Corrigendum: Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis.
- Published in:
- 2009
- By:
- Publication type:
- Correction notice
Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis.
- Published in:
- Nature Genetics, 2008, v. 40, n. 9, p. 1103, doi. 10.1038/ng.198
- By:
- Publication type:
- Article
Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis.
- Published in:
- Nature Genetics, 2008, v. 40, n. 6, p. 713, doi. 10.1038/ng.148
- By:
- Publication type:
- Article