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Isolated Bladder Exstrophy Associated with a De Novo 0.9 Mb Microduplication on Chromosome 19p1312DRAAKEN, Markus; MUGHAL, Sadaf S; BOEMERS, Thomas M et al.Birth defects research. Clinical and molecular teratology. 2013, Vol 97, Num 3, pp 133-139, issn 1542-0752, 7 p.Article

Identification of loci associated with schizophrenia by genome-wide association and follow-upO'DONOVAN, Michael C; CRADDOCK, Nicholas; DWYER, Sarah et al.Nature genetics. 2008, Vol 40, Num 9, pp 1053-1055, issn 1061-4036, 3 p.Article

Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissuePERNHORST, Katharina; LOO, Karen M. J. Van; BECKER, Albert J et al.Brain research. 2013, Vol 1499, pp 136-144, issn 0006-8993, 9 p.Article

Association Between Copy Number Variants in 16p11.2 and Major Depressive Disorder in a German Case—Control SampleDEGENHARDT, Franziska; PRIEBE, Lutz; LANGE, Christoph et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2012, Vol 159, Num 3, pp 263-273, issn 1552-4841, 11 p.Article

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorderMÜHLEISEN, Thomas W; MATTHEISEN, Manuel; RIVANDENEIRA, Fernando et al.Schizophrenia research. 2012, Vol 138, Num 1, pp 69-73, issn 0920-9964, 5 p.Article

Mapping for Dyslexia and Related Cognitive Trait Loci Provides Strong Evidence for Further Risk Genes on Chromosome 6p21KÖNIG, Inke R; SCHUMACHER, Johannes; PROPPING, Peter et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2011, Vol 156, Num 1, pp 36-43, issn 1552-4841, 8 p.Article

Inhibition of hepatitis C virus RNA translation by antisense bile acid conjugated phosphorothioate modified oligodeoxynucleotides (ODN)GONZALEZ-CARMONA, Maria A; QUASDORFF, Maria; SAUERBRUCH, Tilman et al.Antiviral research. 2013, Vol 97, Num 1, pp 49-59, issn 0166-3542, 11 p.Article

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma riskBRODERICK, Peter; CHUBB, Daniel; DAVIES, Faith E et al.Nature genetics. 2012, Vol 44, Num 1, pp 58-61, issn 1061-4036, 4 p.Article

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunityTSOI, Lam C; SPAIN, Sarah L; KANG, Hyun M et al.Nature genetics. 2012, Vol 44, Num 12, pp 1341-1348, issn 1061-4036, 8 p.Article

Inhibition of hepatitis C virus gene expression by adenoviral vectors encoding antisense RNA in vitro and in vivoGONZALEZ-CARMONA, Maria A; VOGT, Annabelle; CASELMANN, Wolfgang H et al.Journal of hepatology. 2011, Vol 55, Num 1, pp 19-28, issn 0168-8278, 10 p.Article

Replication of Novel Susceptibility Locus for Nonsyndromic Cleft Lip With or Without Cleft Palate on Chromosome 8q24 in Estonian and Lithuanian PatientsNIKOPENSIUS, Tiit; AMBROZAITYTE, Laima; HOFFMANN, Per et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 11, pp 2551-2553, issn 1552-4825, 3 p.Article

Investigation of the involvement of MIR185 and its target genes in the development of schizophreniaFORSTNER, Andreas J; BASMANAV, F. Buket; HERMS, Stefan et al.Journal of psychiatry & neuroscience. 2014, Vol 39, Num 6, pp 386-396, issn 1180-4882, 11 p.Article

αCaMKII Autophosphorylation Controls the Establishment of Alcohol Drinking BehaviorEASTON, Alanna C; LUCCHESI, Walter; MOLL, Gunther H et al.Neuropsychopharmacology (New York, NY). 2013, Vol 38, Num 9, pp 1636-1647, issn 0893-133X, 12 p.Article

Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literatureSCHRAMM, Charlotte; DRAAKEN, Markus; KREISS-NACHTSHEIM, Martina et al.European journal of pediatrics. 2011, Vol 170, Num 6, pp 741-746, issn 0340-6199, 6 p.Article

Disruption of the neurexin 1 gene is associated with schizophreniaRUJESCU, Dan; INGASON, Andres; MURRAY, Robin et al.Human molecular genetics (Print). 2009, Vol 18, Num 5, pp 988-996, issn 0964-6906, 9 p.Article

Hammerhead ribozymes with cleavage site specificity for NUH and NCH display significant anti-hepatitis C viral effect in vitro and in recombinant HepG2 and CCL13 cellsGONZALEZ-CARMONA, Maria-Angeles; SCHÜSSLER, Sabine; CASELMANN, Wolfgang H et al.Journal of hepatology. 2006, Vol 44, Num 6, pp 1017-1025, issn 0168-8278, 9 p.Article

Imaging genetics of FOXP2 in dyslexiaWILCKE, Arndt; LIGGES, Carolin; CICHON, Sven et al.European journal of human genetics. 2012, Vol 20, Num 2, pp 224-229, issn 1018-4813, 6 p.Article

Direct Conversion of Fibroblasts into Stably Expandable Neural Stem CellsTHIER, Marc; WÖRSDÖRFER, Philipp; BRÜSTLE, Oliver et al.Cell stem cell. 2012, Vol 10, Num 4, pp 473-479, issn 1934-5909, 7 p.Article

De Novo Duplication of 18p11.21-18q12.1 in a Female With Anorectal NialformationSCHRAMM, Charlotte; DRAAKEN, Markus; PRIEBE, Lutz et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 445-449, issn 1552-4825, 5 p.Article

Common variation at 10p12.31 near MLLT10 influences meningioma riskDOBBINS, Sara E; BRODERICK, Peter; MA, Yussanne P et al.Nature genetics. 2011, Vol 43, Num 9, pp 825-827, issn 1061-4036, 3 p.Article

Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph diseaseKOCH, Philipp; BREUER, Peter; HOFFMANN, Per et al.Nature (London). 2011, Vol 480, Num 7378, pp 543-546, issn 0028-0836, 4 p.Article

A locus on 2p12 containing the co-regulated MRPL 19 and C2ORF3 genes is associated to dyslexiaANTHONI, Heidi; ZUCCHELLI, Marco; HOFFMANN, Per et al.Human molecular genetics (Print). 2007, Vol 16, Num 6, pp 667-677, issn 0964-6906, 11 p.Article

The Bremen Cog of 1380: An electron microscopic study of its degraded wood before and after stabilization with PEGHOFFMANN, Per; SINGH, Adya; YOON SOO KIM et al.Holzforschung. 2004, Vol 58, Num 3, pp 211-218, issn 0018-3830, 8 p.Article

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk lociLUDWIG, Kerstin U; MANGOLD, Elisabeth; BÖHMER, Anne C et al.Nature genetics. 2012, Vol 44, Num 9, pp 968-971, issn 1061-4036, 4 p.Article

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophreniaMATTHEISEN, Manuel; MUHLEISEN, Thomas W; WITT, Stephanie H et al.Schizophrenia research. 2012, Vol 141, Num 2-3, pp 262-265, issn 0920-9964, 4 p.Article

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