Diana Hall

Publications | Mémoires et thèses

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29 publications

2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2011 | 2010 | 2008 | 2004 | 2003 | 2002 | 2001 | 1999 | 1995 |
 
Correction: Analysis of fetal DNA in maternal plasma with markers designed for forensic DNA mixture resolution
Moriot A., Hall D., 2019/07. 1.
Analysis of fetal DNA in maternal plasma with markers designed for forensic DNA mixture resolution.
Moriot A., Hall D., 2019/03. Genetics in medicine, 21 (3) pp. 613-621. Peer-reviewed.
Inferring biogeographic ancestry with compound markers of slow and fast evolving polymorphisms.
Moriot A., Santos C., Freire-Aradas A., Phillips C., Hall D., 2018/11. European journal of human genetics, 26 (11) pp. 1697-1707. Peer-reviewed.
 
Application of DIP-STRs to sexual/physical assault investigations: Eight case reports.
Oldoni F., Castella V., Hall D., 2017/09. Forensic science international. Genetics, 30 pp. 106-113. Peer-reviewed.
 
Sensitive DIP-STR markers for the analysis of unbalanced mixtures from "touch" DNA samples.
Oldoni F., Castella V., Grosjean F., Hall D., 2017/02/14. Forensic science international. Genetics, 28 pp. 111-117. Peer-reviewed.
 
Shedding light on the relative DNA contribution of two persons handling the same object.
Oldoni F., Castella V., Hall D., 2016. Forensic Science International. Genetics, 24 (5) pp. 148-157. Peer-reviewed.
 
A novel set of DIP-STR markers for improved analysis of challenging DNA mixtures.
Oldoni F., Castella V., Hall D., 2015/11. Forensic science international. Genetics, 19 pp. 156-164. Peer-reviewed.
 
Exploring the relative DNA contribution of first and second object's users on mock touch DNA mixtures
Oldoni F., Castella V., Hall D., 2015. Forensic Science International: Genetics Supplement Series, 5 pp. e300-e301. Peer-reviewed.
 
An investigation of the potential of DIP-STR markers for DNA mixture analyses
Cereda G., Biedermann A., Hall D., Taroni F., 2014. Forensic Science International. Genetics, 11 pp. 229-240.
 
Object-oriented Bayesian networks for evaluating DIP-STR profiling results from unbalanced DNA mixtures.
Cereda G., Biedermann A., Hall D., Taroni F., 2014/01. Forensic Science International. Genetics, 8 (1) pp. 159-169. Peer-reviewed.
DIP-STR: Highly Sensitive Markers for the Analysis of Unbalanced Genomic Mixtures.
Castella V., Gervaix J., Hall D., 2013. Human Mutation, 34 (4) pp. 644-654.
 
Preuve par l'ADN: la génétique au service de la justice
Coquoz R., Comte J., Hall D., Hicks T., Taroni F., 2013., 3e éd. rev. et augm. 457, Presses polytechniques et universitaires romandes.
 
DIP-STR: A new marker for resolving unbalanced DNA mixtures
Hall D., Castella V., 2011. Forensic Science International: Genetics Supplement Series, 3 pp. e1-e2.
 
DNA extraction using the QIAsymphony: Evaluation of PCR inhibitor removal
Castella V., Kummer D., Gehrig C., Hall D., 2011. Forensic Science International: Genetics Supplement Series, 3 pp. e69-e-70.
Oxidative phosphorylation flexibility in the liver of mice resistant to high-fat diet-induced hepatic steatosis.
Poussin C., Ibberson M., Hall D., Ding J., Soto J., Abel E.D., Thorens B., 2011. Diabetes, 60 (9) pp. 2216-2224.
 
Peroxisomal and microsomal lipid pathways associated with resistance to hepatic steatosis and reduced pro-inflammatory state.
Hall D., Poussin C., Velagapudi V.R., Empsen C., Joffraud M., Beckmann J.S., Geerts A.E., Ravussin Y., Ibberson M., Oresic M. et al., 2010. Journal of Biological Chemistry, 285 (40) pp. 31011-31023.
FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
Leehey M.A., Berry-Kravis E., Goetz C.G., Zhang L., Hall D.A., Li L., Rice C.D., Lara R., Cogswell J., Reynolds A. et al., 2008/12. Neurology, 70 (16 Pt 2) pp. 1397-1402. Peer-reviewed.
Different transcriptional control of metabolism and extracellular matrix in visceral and subcutaneous fat of obese and rimonabant treated mice.
Poussin C., Hall D., Minehira K., Galzin A.M., Tarussio D., Thorens B., 2008. PLoS ONE, 3 (10) pp. e3385. Peer-reviewed.
 
Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia.
Emamian E.S., Hall D., Birnbaum M.J., Karayiorgou M., Gogos J.A., 2004. Nature Genetics, 36 (2) pp. 131-137.
 
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.
Abecasis G.R., Burt R.A., Hall D., Bochum S., Doheny K.F., Lundy S.L., Torrington M., Roos J.L., Gogos J.A., Karayiorgou M., 2004. American Journal of Human Genetics, 74 (3) pp. 403-417.
 
The contribution of three strong candidate schizophrenia susceptibility genes in demographically distinct populations.
Hall D., Gogos J.A., Karayiorgou M., 2004. Genes, Brain, and Behavior, 3 (4) pp. 240-248.
 
Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit.
Gerber D.J., Hall D., Miyakawa T., Demars S., Gogos J.A., Karayiorgou M., Tonegawa S., 2003. Proceedings of the National Academy of Sciences of the United States of America, 100 (15) pp. 8993-8998.
 
Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q.
Wijsman E.M., Rosenthal E.A., Hall D., Blundell M.L., Sobin C., Heath S.C., Williams R., Brownstein M.J., Gogos J.A., Karayiorgou M., 2003. Molecular Psychiatry, 8 (7) pp. 695-705, 643. Peer-reviewed.
 
Sequence variants of the brain-derived neurotrophic factor (BDNF) gene are strongly associated with obsessive-compulsive disorder.
Hall D., Dhilla A., Charalambous A., Gogos J.A., Karayiorgou M., 2003. American Journal of Human Genetics, 73 (2) pp. 370-376.
 
Extended intermarker linkage disequilibrium in the Afrikaners.
Hall D., Wijsman E.M., Roos J.L., Gogos J.A., Karayiorgou M., 2002. Genome Research, 12 (6) pp. 956-961.
 
A repository of 14 PCR-loci Italian gene frequencies in the World Wide Web.
Maviglia R., Dobosz M., Boschi I., Caglià A., Hall D., Capelli C., d'Aloja E., Pescarmona M., Moscetti A., Pascali V.L. et al., 2001. Forensic Science International, 115 (1-2) pp. 99-101.
 
Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism.
Iyer L., Hall D., Das S., Mortell M.A., Ramírez J., Kim S., Di Rienzo A., Ratain M.J., 1999. Clinical Pharmacology and Therapeutics, 65 (5) pp. 576-582.
 
Variability at the uridine diphosphate glucuronosyltransferase 1A1 promoter in human populations and primates.
Hall D., Ybazeta G., Destro-Bisol G., Petzl-Erler M.L., Di Rienzo A., 1999. Pharmacogenetics, 9 (5) pp. 591-599.
 
Identification of the cis-elements mediating the autogenous control of ribosomal protein L2 mRNA stability in yeast.
Presutti C., Villa T., Hall D., Pertica C., Bozzoni I., 1995. Embo Journal, 14 (16) pp. 4022-4030.
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