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Forensic evaluation of Y-STR haplotype matches : a commentKRAWCZAK, Michael.Forensic science international. 2001, Vol 118, Num 2-3, pp 114-115, issn 0379-0738Article

ASP: a simulation-based power calculator for genetic linkage studies of qualitative traits, using sib-pairsKRAWCZAK, Michael.Human genetics. 2001, Vol 109, Num 6, pp 675-677, issn 0340-6717Article

Estimating the efficacy and efficiency of cascade genetic screeningKRAWCZAK, Michael; COOPER, David N; SCHMIDTKE, Jörg et al.American journal of human genetics. 2001, Vol 69, Num 2, pp 361-370, issn 0002-9297Article

Forensic interpretation of Y-chromosomal DNA mixturesWOLF, Andreas; CALIEBE, Amke; JUNGE, Olaf et al.Forensic science international. 2005, Vol 152, Num 2-3, pp 209-213, issn 0379-0738, 5 p.Article

Population genetics of Y-chromosomal microsatellites in Baltic malesLESSIG, Rüdiger; EDELMANN, Jeanett; KRAWCZAK, Michael et al.Forensic science international. 2001, Vol 118, Num 2-3, pp 153-157, issn 0379-0738Article

Entropy-based SNP selection for genetic association studiesHAMPE, Jochen; SCHREIBER, Stefan; KRAWCZAK, Michael et al.Human genetics. 2003, Vol 114, Num 1, pp 36-43, issn 0340-6717, 8 p.Article

A comprehensive evaluation of SNP genotype imputationNOTHNAGEL, Michael; ELLINGHAUS, David; SCHREIBER, Stefan et al.Human genetics. 2009, Vol 125, Num 2, pp 163-171, issn 0340-6717, 9 p.Article

Genomic and geographic distribution of SNP-defined runs of homozygosity in EuropeansNOTHNAGEL, Michael; TEHUA LU, Timothy; KAYSER, Manfred et al.Human molecular genetics (Print). 2010, Vol 19, Num 15, pp 2927-2935, issn 0964-6906, 9 p.Article

Genetics of Crohn disease, an archetypal inflammatory barrier diseaseSCHREIBER, Stefan; ROSENSTIEL, Philip; ALBRECHT, Mario et al.Nature reviews. Genetics (Print). 2005, Vol 6, Num 5, pp 376-388, issn 1471-0056, 13 p.Article

Biobanking and international interoperability: samplesKIEHNTOPF, Michael; KRAWCZAK, Michael.Human genetics. 2011, Vol 130, Num 3, pp 369-376, issn 0340-6717, 8 p.Article

An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European populationTEHUA LU, Timothy; LAO, Oscar; HOLMLUND, Gunilla et al.European journal of human genetics. 2009, Vol 17, Num 7, pp 967-975, issn 1018-4813, 9 p.Article

Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosisHOFMANN, Sylvia; FRANKE, Andre; SCHREIBER, Stefan et al.Nature genetics. 2008, Vol 40, Num 9, pp 1103-1106, issn 1061-4036, 4 p.Article

A legal framework for biobanking : the German experienceSIMON, Jürgen; PASLACK, Rainer; ROBIENSKI, Jürgen et al.European journal of human genetics. 2007, Vol 15, Num 5, pp 528-532, issn 1018-4813, 5 p.Article

Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaquesSAUERMANN, Ulrike; NÜRNBERG, Peter; BERCOVITCH, Fred B et al.Human genetics. 2001, Vol 108, Num 3, pp 249-254, issn 0340-6717Article

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in EuropeHASTINGS, Ros; DE WERT, Guido; SCHMIDTKE, Jörg et al.European journal of human genetics. 2012, Vol 20, Num 9, pp 911-916, issn 1018-4813, 6 p.Article

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities: Background Document to the ESHG recommendations on genetic testing and common disordersBECKER, Frauke; VAN EL, Carla G; JANSSENS, A. Cecile Jw et al.European journal of human genetics. 2011, Vol 19, issn 1018-4813, S6-S44, SUP1Article

Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibilityFRANKE, Andre; BALSCHUN, Tobias; SINA, Christian et al.Nature genetics. 2008, Vol 40, Num 11, pp 1319-1323, issn 1061-4036, 5 p.Article

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1HAMPE, Jochen; FRANKE, Andre; GÜNTHER, Simone et al.Nature genetics. 2007, Vol 39, Num 2, pp 207-211, issn 1061-4036, 5 p.Article

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populationsCROUCHER, Peter J. P; MASCHERETTI, Silvia; WON HO KIM et al.European journal of human genetics. 2003, Vol 11, Num 1, pp 6-16, issn 1018-4813, 11 p.Article

Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regionsKRAWCZAK, Michael; CHUZHANOVA, Nadia A; STENSON, Peter D et al.Human genetics. 2000, Vol 107, Num 4, pp 362-365, issn 0340-6717Article

Homozygosity for a conserved Mhc class II DQ-DRB haplotype is associated with rapid disease progression in simian immunodeficiency virus-infected macaques : Results from a prospective studySAUERMANN, Ulrike; STAHL-HENNIG, Christiane; STOLTE, Nicole et al.The Journal of infectious diseases. 2000, Vol 182, Num 3, pp 716-724, issn 0022-1899Article

Technology-specific error signatures in the 1000 Genomes Project dataNOTHNAGEL, Michael; HERRMANN, Alexander; WOLF, Andreas et al.Human genetics. 2011, Vol 130, Num 4, pp 505-516, issn 0340-6717, 12 p.Article

A functional EXO1 promoter variant is associated with prolonged life expectancy in centenariansNEBEL, Almut; FTACHSBART, Friederike; BINGHUI SHEN et al.Mechanisms of ageing and development. 2009, Vol 130, Num 10, pp 691-699, issn 0047-6374, 9 p.Article

On the Use of General Control Samples for Genome-wide Association Studies : Genetic Matching Highlights Causal VariantsLUCA, Diana; RINGQUIST, Steven; DEVLIN, Bernie et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 453-463, issn 0002-9297, 11 p.Article

Plastin 3 Is a Protective Modifier of Autosomal Recessive Spinal Muscular AtrophyOPREA, Gabriela E; KRÖBER, Sandra; MCWHORTER, Michelle L et al.Science (Washington, D.C.). 2008, Vol 320, Num 5875, pp 524-527, issn 0036-8075, 4 p.Article

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