Genetics (Methods)

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Genetics (Methods)

LE WE PMID CA

Genetics (Methods)

988

Genetik (Methoden)

Bacteria (Taxonomy)

Bayesian statistics

Biobank Repository

Biodiversity

Chromatin immunoprecipitation

Data base (Medicine Biology Pharmacology)

ENU mutagenesis

Enzyclopedical

Expressed sequence tags

Forensic medicine

Genetics (GWAS Genome wide association study)

Genetics (Linkage disequilibrium)

Genetics (Methods)

Genetics (Positional cloning)

Genetics (Quantitative trait locus)

Genetics (Reverse genetics)

Genomic signatures

Laboratory animal (Mouse)

RNA (BASKET)

Systems biology

2007 1	Introduction to genetic association studies. [17853910] J Invest Dermatol 127(10): 2283-7 (2007)
2001 2	Genome-wide ENU mutagenesis to reveal immune regulators. [11567631] Immunity 15(3): 409-18 (2001)
2009 3	Genome and proteome annotation: organization, interpretation and integration. [19019817] J R Soc Interface 6(31): 129-47 (2009)
2007 4	Approaches to handling incomplete data in family-based association testing. [17096676] Ann Hum Genet 71(Pt 2): 141-51 (2007)
2000 5	Applications of the estimating equations theory to genetic epidemiology: a review. [11388891] Ann Hum Genet 64(Pt 1): 1-14 (2000)
1998 6	TDT statistics for mapping quantitative trait loci. [10088040] Ann Hum Genet 62(Pt 5): 431-52 (1998)
2009 7	Mouse models of genomic syndromes as tools for understanding the basis of complex traits: an example with the smith-magenis and the potocki-lupski syndromes. [19949547] Curr Genomics 10(4): 259-68 (2009)
2009 8	Hidden Markov Models and their Applications in Biological Sequence Analysis. [20190955] Curr Genomics 10(6): 402-15 (2009)
2006 9	Extracting haplotypes from diploid organisms. [16875417] Curr Issues Mol Biol 8(2): 113-22 (2006)
2004 10	Comparative genomic hybridization (CGH)-arrays pave the way for identification of novel cancer-related genes. [15245590] Cancer Sci 95(7): 559-63 (2004)
2008 11	Bayesian meta-analysis of genetic association studies with different sets of markers. [18394581] Am J Hum Genet 82(4): 859-72 (2008)
2008 12	Robust score statistics for QTL linkage analysis. [18304491] Am J Hum Genet 82(3): 567-82 (2008)
2008 13	A unified association analysis approach for family and unrelated samples correcting for stratification. [18252216] Am J Hum Genet 82(2): 352-65 (2008)
2007 14	New perspectives for the elucidation of genetic disorders. [17668371] Am J Hum Genet 81(2): 199-207 (2007)
2007 15	Genome scanning by composite likelihood. [17160891] Am J Hum Genet 80(1): 19-28 (2007)
2005 16	Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p. [16380906] Am J Hum Genet 77(6): 937-44 (2005)
2005 17	Recent developments in genomewide association scans: a workshop summary and review. [16080110] Am J Hum Genet 77(3): 337-45 (2005)
2005 18	Nonparametric tests of association of multiple genes with human disease. [15786018] Am J Hum Genet 76(5): 780-93 (2005)
2004 19	Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps. [15311375] Am J Hum Genet 75(4): 687-92 (2004)
2004 20	The future of association studies: gene-based analysis and replication. [15272419] Am J Hum Genet 75(3): 353-62 (2004)
2003 21	A comparison of bayesian methods for haplotype reconstruction from population genotype data. [14574645] Am J Hum Genet 73(5): 1162-9 (2003)
2003 22	Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis. [12802787] Am J Hum Genet 73(1): 17-33 (2003)
2003 23	Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. [12802786] Am J Hum Genet 73(1): 34-48 (2003)
2003 24	Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. [12802785] Am J Hum Genet 73(1): 49-62 (2003)
2003 25	Hot and cold spots of recombination in the human genome: the reason we should find them and how this can be achieved. [12772086] Am J Hum Genet 73(1): 5-16 (2003)
2002 26	Meta-analysis of genetic-linkage analysis of quantitative-trait loci. [12037716] Am J Hum Genet 71(1): 56-65 (2002)
2002 27	Score tests for association between traits and haplotypes when linkage phase is ambiguous. [11791212] Am J Hum Genet 70(2): 425-34 (2002)
2001 28	Genomewide scans of complex human diseases: true linkage is hard to find. [11565063] Am J Hum Genet 69(5): 936-50 (2001)
2000 29	Statistical approaches to gene mapping. [10884361] Am J Hum Genet 67(2): 289-94 (2000)
1999 30	Power of association and linkage tests when the disease alleles are unobserved. [9973303] Am J Hum Genet 64(2): 641-9 (1999)
1994 31	Comparative genomic hybridization: an overview. [7992829] Am J Pathol 145(6): 1253-60 (1994)
2008 32	Whole genome scanning as a cytogenetic tool in hematologic malignancies. [18505780] Blood 112(4): 965-74 (2008)
2005 33	Identifying genomic regions for fine-mapping using genome scan meta-analysis (GSMA) to identify the minimum regions of maximum significance (MRMS) across populations. [16451653] BMC Genet 6 Suppl 1(-): S42 (2005)
2002 34	Perspective: how to make microarray, serial analysis of gene expression, and proteomic relevant to day-to-day endocrine problems and physiological systems. [12021160] Endocrinology 143(6): 1995-2001 (2002)
2008 35	Identification of human haploinsufficient genes and their genomic proximity to segmental duplications. [18523451] Eur J Hum Genet 16(11): 1350-7 (2008)
2008 36	Gene-environment interactions for complex traits: definitions, methodological requirements and challenges. [18523454] Eur J Hum Genet 16(10): 1164-72 (2008)
2008 37	The success of the genome-wide association approach: a brief story of a long struggle. [18285837] Eur J Hum Genet 16(5): 554-64 (2008)
2007 38	Guidelines for molecular karyotyping in constitutional genetic diagnosis. [17637806] Eur J Hum Genet 15(11): 1105-14 (2007)
2007 39	Meta-analysis of genome-wide linkage studies for multiple sclerosis, using an extended GSMA method. [17377519] Eur J Hum Genet 15(6): 703-10 (2007)
2006 40	Recent advances in array comparative genomic hybridization technologies and their applications in human genetics. [16288307] Eur J Hum Genet 14(2): 139-48 (2006)
1998 41	Parallel molecular genetic analysis. [9801865] Eur J Hum Genet 6(5): 417-29 (1998)
1998 42	Modifier genes in humans: strategies for identification. [9781018] Eur J Hum Genet 6(1): 80-8 (1998)
2008 43	Genome-wide association studies: potential next steps on a genetic journey. [18852205] Hum Mol Genet 17(R2): R156-65 (2008)
2008 44	Genome-wide association studies: past, present and future. [18852196] Hum Mol Genet 17(R2): R100-1 (2008)
2008 45	A HapMap harvest of insights into the genetics of common disease. [18451988] J Clin Invest 118(5): 1590-605 (2008)
2005 46	Mapping quantitative trait loci in humans: achievements and limitations. [15931376] J Clin Invest 115(6): 1419-24 (2005)
2005 47	Factors affecting statistical power in the detection of genetic association. [15931375] J Clin Invest 115(6): 1408-18 (2005)
2007 48	Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Multi-organ whole-genome measurements and reverse engineering to uncover gene networks underlying complex traits. [17142807] J Lipid Res 48(2): 267-77 (2007)
1984 49	Blot hybridisation analysis of genomic DNA. [6086927] J Med Genet 21(3): 164-72 (1984)
2003 50	Primer on medical genomics. Part VIII: Essentials of medical genetics for the practicing physician. [12839081] Mayo Clin Proc 78(7): 846-57 (2003)
2003 51	Primer on medical genomics. Part VII: The evolving concept of the gene. [12744545] Mayo Clin Proc 78(5): 580-7 (2003)
2003 52	Primer on medical genomics. Part VI: Genomics and molecular genetics in clinical practice. [12630584] Mayo Clin Proc 78(3): 307-17 (2003)
2003 53	Primer on medical genomics part V: bioinformatics. [12528878] Mayo Clin Proc 78(1): 57-64 (2003)
2002 54	Primer on medical genomics part II: Background principles and methods in molecular genetics. [12173714] Mayo Clin Proc 77(8): 785-808 (2002)
1999 55	Comparative genomic hybridisation. [10748872] Mol Pathol 52(5): 243-51 (1999)
2009 56	Genome-wide association studies--a summary for the clinical gastroenterologist. [19916168] World J Gastroenterol 15(43): 5377-96 (2009)
2005 57	Genotyping microarray for the detection of more than 200 CFTR mutations in ethnically diverse populations. [16049310] J Mol Diagn 7(3): 375-87 (2005)
2002 58	Methods of molecular analysis: mutation detection in solid tumours. [11950952] Mol Pathol 55(2): 73-9 (2002)
2009 59	Multilocus Bayesian meta-analysis of gene-disease associations. [19409523] Am J Hum Genet 84(5): 567-80 (2009)
2009 60	Genetics of Graves' disease: the lost concept. [19258680] Acta Med Indones 41(1): 37-40 (2009)
2010 61	Metabolic networks: how to identify key components in the regulation of metabolism and growth. [20018593] Plant Physiol 152(2): 428-44 (2010)
2005 62	Genetic testing: practical, ethical, and counseling considerations. [15667031] Mayo Clin Proc 80(1): 63-73 (2005)
2010 63	New surprises from the deep--the family of small regulatory RNAs increases. [20602081] ScientificWorldJournal 10(-): 1239-43 (2010)
2011 64	Reverse genetic strategies in Caenorhabditis elegans: towards controlled manipulation of the genome. [21789474] ScientificWorldJournal 11(-): 1394-410 (2011)
2011 65	Genomic signatures in microbes -- properties and applications. [21442149] ScientificWorldJournal 11(-): 715-25 (2011)
2003 66	Genetic epidemiology, genetic maps and positional cloning. [14561327] Philos Trans R Soc Lond B Biol Sci 358(1438): 1701-8 (2003)
2007 67	Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays. [17363572] Cancer Res 67(6): 2544-51 (2007)
2007 68	Quantitative heteroduplex analysis. [17517584] Clin Chem 53(6): 1001-3 (2007)
2009 69	Next-generation sequencing: from basic research to diagnostics. [19246620] Clin Chem 55(4): 641-58 (2009)
2008 70	Molecular diagnostics in genodermatoses - simplified. [18187815] Indian J Dermatol Venereol Leprol 74(1): 8-14 (2008)
2006 71	Statistical methods in genetics. [16963464] Brief Bioinform 7(3): 297-308 (2006)
2002 72	Genetic association studies: design, analysis and interpretation. [12139434] Brief Bioinform 3(2): 146-53 (2002)
2010 73	Semiparametric prognosis models in genomic studies. [20123942] Brief Bioinform 11(4): 385-93 (2010)
2007 74	A hitchhiker's guide to expressed sequence tag (EST) analysis. [16772268] Brief Bioinform 8(1): 6-21 (2007)
2007 75	Partial least squares: a versatile tool for the analysis of high-dimensional genomic data. [16772269] Brief Bioinform 8(1): 32-44 (2007)
2007 76	Forensic DNA and bioinformatics. [17384432] Brief Bioinform 8(2): 117-28 (2007)
2011 77	Strategies for aggregating gene expression data: the collapseRows R function. [21816037] BMC Bioinformatics 12(-): 322 (2011)
2011 78	Deregulation upon DNA damage revealed by joint analysis of context-specific perturbation data. [21693013] BMC Bioinformatics 12(-): 249 (2011)
2007 79	A survey of DNA motif finding algorithms. [18047721] BMC Bioinformatics 8 Suppl 7(-): S21 (2007)
2008 80	Catmap: case-control and TDT meta-analysis package. [18307795] BMC Bioinformatics 9(-): 130 (2008)
2010 81	A brief review of molecular techniques to assess plant diversity. [20559503] Int J Mol Sci 11(5): 2079-96 (2010)
2010 82	Variance component methods for analysis of complex phenotypes. [20439422] Cold Spring Harb Protoc 2010(5): pdb.top77 (2010)
2007 83	Candidate gene identification approach: progress and challenges. [17998950] Int J Biol Sci 3(7): 420-7 (2007)
2009 84	ChIP-based methods for the identification of long-range chromatin interactions. [19247990] J Cell Biochem 107(1): 30-9 (2009)
2009 85	Finding genes underlying human disease. [18783406] Clin Genet 75(2): 101-6 (2009)
2008 86	Breaking loops in large complex pedigrees. [17898536] Hum Hered 65(2): 57-65 (2008)
2006 87	The APL test: extension to general nuclear families and haplotypes and examination of its robustness. [16877866] Hum Hered 61(4): 189-99 (2006)
2009 88	Genetic tools and algorithms for gene discovery in major congenital anomalies. [19107955] Birth Defects Res A Clin Mol Teratol 85(1): 6-12 (2009)
2009 89	QTL global meta-analysis: are trait determining genes clustered? [19393059] BMC Genomics 10(): 184 (2009)
2011 90	A genetical genomics approach to genome scans increases power for QTL mapping. [21196521] Genetics 187(3): 939-53 (2011)
2011 91	Bayesian multiple quantitative trait loci mapping for recombinant inbred intercrosses. [21385723] Genetics 188(1): 189-95 (2011)
2004 92	On the Metropolis-Hastings acceptance probability to add or drop a quantitative trait locus in Markov chain Monte Carlo-based Bayesian analyses. [15020452] Genetics 166(1): 641-3 (2004)
2006 93	Genetic mapping and manipulation: chapter 2--Two-point mapping with genetic markers. [18050462] WormBook -(-): 1-6 (2006)
2006 94	Genetic mapping and manipulation: chapter 6--Mapping with deficiencies and duplications. [18050458] WormBook -(-): 1-3 (2006)
2006 95	Genetic mapping and manipulation: chapter 7--Making compound mutants. [18050457] WormBook -(-): 1-4 (2006)
2006 96	Genetic dissection of developmental pathways. [18050452] WormBook -(-): 1-19 (2006)
2006 97	RNA in situ hybridization of dissected gonads. [18050448] WormBook -(-): 1-7 (2006)
2006 98	Protocols for large scale in situ hybridization on C. elegans larvae. [18050447] WormBook -(-): 1-8 (2006)

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