Diana Hall

Publications | Mémoires et thèses

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33 publications

2024 | 2023 | 2021 | 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2011 | 2010 | 2008 | 2004 | 2003 | 2002 | 2001 | 1999 | 1995 |
2024
Differentiation of five forensically relevant body fluids using a small set of microRNA markers.
Altmeyer L., Baumer K., Hall D., 2024/10. Electrophoresis, 45 (19-20) pp. 1785-1795. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_42D1E66B9EB8]
2023
Early noninvasive prenatal paternity testing by targeted fetal DNA analysis.
Damour G., Baumer K., Legardeur H., Hall D., 2023/07/26. Scientific reports, 13 (1) p. 12139. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_E8EC3180DA38]
 
Identification and characterization of novel DIP-STRs from whole-genome sequencing data.
Damour G., Mauffrey F., Hall D., 2023/05. Forensic science international. Genetics, 64 p. 102849. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_BB4C7E64E112]
2021
Further insight into the global variability of the OCA2-HERC2 locus for human pigmentation from multiallelic markers.
Suarez P., Baumer K., Hall D., 2021/11/18. Scientific reports, 11 (1) p. 22530. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_10AF8DB19C52]
2019
 
Correction: Analysis of fetal DNA in maternal plasma with markers designed for forensic DNA mixture resolution
Moriot A., Hall D., 2019/07. 1.
[DOI][WoS][Pmid][serval:BIB_FA36BFDF1E7A]
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.
[URN][DOI][WoS][Pmid][serval:BIB_39BEF9A322ED]
2018
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.
[URN][DOI][WoS][Pmid][serval:BIB_86FB912BC94A]
2017
 
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.
[DOI][WoS][Pmid][serval:BIB_2364B002C4AA]
 
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.
[DOI][WoS][Pmid][serval:BIB_E16EB8BDFC5B]
2016
 
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.
[DOI][WoS][Pmid][serval:BIB_7311C6F0A9C3]
2015
 
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.
[DOI][WoS][Pmid][serval:BIB_FE077B1E4AFD]
 
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.
[URN][DOI][WoS][serval:BIB_C0D8F3E2A3DF]
2014
 
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.
[DOI][WoS][Pmid][serval:BIB_6BBD5A3197FC]
 
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.
[DOI][WoS][Pmid][serval:BIB_440E0D06230F]
2013
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.
[URN][DOI][WoS][Pmid][serval:BIB_2E06998C6441]
 
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.
[serval:BIB_45436ABA1B0C]
2011
 
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.
[DOI][serval:BIB_1F360559B904]
 
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.
[DOI][serval:BIB_BBBA484BA3AF]
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.
[URN][DOI][WoS][Pmid][serval:BIB_90E2A4ED2946]
2010
 
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.
[DOI][WoS][Pmid][serval:BIB_5C7339688FC7]
2008
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.
[DOI][WoS][Pmid][serval:BIB_C6865B44438D]
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.
[URN][DOI][WoS][Pmid][serval:BIB_ED5FF5045C10]
2004
 
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.
[DOI][Pmid][serval:BIB_96DE20E0AEF6]
 
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.
[DOI][Pmid][serval:BIB_9C3F8042C2D4]
 
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.
[DOI][Pmid][serval:BIB_301BA1B0C008]
2003
 
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.
[DOI][Pmid][serval:BIB_265FA81F58C0]
 
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.
[DOI][Pmid][serval:BIB_5F510E424560]
 
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.
[DOI][Pmid][serval:BIB_B0F3C01E6AD8]
2002
 
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.
[DOI][Pmid][serval:BIB_0B474EF22857]
2001
 
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.
[Pmid][serval:BIB_7CFEA11E0747]
1999
 
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.
[DOI][Pmid][serval:BIB_4B100A96DC0B]
 
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.
[Pmid][serval:BIB_D3E5F42B66DD]
1995
 
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.
[Pmid][serval:BIB_0CE29EE76F4A]
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