PUBLIKATIONER
Rättsgenetik, Linköping 1991 – 2014
1991
1. Lindblom B, Holmlund G, Stennek A. DNA-analyser i
rättsgenetiska utredningar. Läkartidningen 1991;88:2055-9.
2. Afoke A, Ludvigsson J, Hed J, Lindblom B. Raised IgG and IgM in
"epidemic" IDDM suggest that infections are responsible for the seasonality
of type I diabetes. Diabetes Res 1991;16:11-7.
1992
3. Kihlström E, Foberg U, Bengtsson A, Frydén A, Svenungsson B, Schvarcz,
Lindblom B, Castor B. Intestinal symptoms and serological response in
patients with complicated and uncomplicated Yersinia enterocolitica
infections. Scand J Infect Dis 1992;24:57-63.
4. Holmlund G, Karlberg K, Gustavsson B, Lindblom B. Calculation
of Restriction Fragment Lengths by Image Processing.
Electrophoresis 1992;13: 407-10.
1993
5. Afoke AO, Eeg-Olofsson O, Hed J, Kjellman NI, Lindblom B, Ludvigsson J.
Seasonal variation and sex differences of circulating macrophages,
immunoglobulins and lymphocytes in healthy school children. 41. Scand J
Immunol 1993;37:209-15.
6. Langö A, Lindblom B. HLA DQA-DQB haplotypes in a Swedish population.
Eur J Immunogenet 1993;20(6):453-60.
7. Dahlén GH, Slunga L, Holmlund G, Langö A, Lindblom B. Lp(a)
Lipoprotein and HLA-DR Genotype in Early Coronary Artery Disease. A
Pilot study. Eur. J. Immunogenetics. 1993;20:95-102.
1994
8. Holmlund G, Wahlgren B, Lindblom B. A D12S11 (MS43A) allele with an
internal HinfI restriction site. Forensic Science International 1994;66:105-9.
1995
9. Dahlén GH, Boman J, Birgander LS, Lindblom B. Lp(a) lipoprotein, IgG,
IgA and IgM antibodies to Chlamydia pneumoniae and HLA class II
genotype in early coronary artery disease. Atherosclerosis 1995;114:165-74.
10. Hildén JO, Gottvall T, Lindblom B. HLA phenotypes and severe Rh(D)
immunization. Tissue Antigens 1995;46:313-5.
11. Holmlund G, Lindblom B. Flanking region sequences and internal repeat
structure of the pYNH24 (D2S44) 2 Kb insert. Electrophoresis 1995;1881-5.
1996
12. Langö-Warensjö A, Cardell K, Lindblom B. Haplotypes comprising subtypes
of the DQB1*06 allele direct the antibody response after immunisation with
hepatitis B surface antigen. 27. Tissue Antigens 1998; 52:374-80.
1997
13. Jonasson L, Eriksson T, Dahlén GH, Lindblom B. Lipoprotein(a) and HLADRB1 and -DQB1 genes in coronary artery disease. 28. Atherosclerosis
1997;133:111-4.
1998
14. Holmlund G, Lindblom B. Different ancestor alleles: A reason for the
bimodal fragment size distribution in the minisatellite D2S44 (YNH24).
European Journal of Human Genetics 1998;6:597-602.
1999
2000
2001
2002
2003
15. Juliusson G, Karlsson K, Malm C, Frödin U, Mollén AS, Bäckström G,
Söderkvist P. Adjusted conditioning for allogeneic transplantation in a single
center setting: mixed chimerism heralds relapse. Leuk Lymphoma 2003
44:669-79.
16. Zackrisson AL, Lindblom B.Identification of CYP2D6 alleles by single
nucleotide polymorphism analysis using pyrosequencing. Eur J Clin
Pharmacol 2003;59:521-6.
2004
17. Holmgren P, Carlsson B, Zackrisson AL, Lindblom B, Dahl ML, Scordo MG,
Druid H, Ahlner J. Enantioselective analysis of citalopram and its metabolites
in postmortem blood and genotyping for CYD2D6 and CYP2C19. J Anal
Toxicol 2004;28:94-104.
18. Zackrisson AL, Holmgren P, Gladh AB, Ahlner J, Lindblom B. Fatal
intoxication cases: cytochrome P450 2D6 and 2C19 genotype
distributions.Eur J Clin Pharmacol 2004;60:547-52.
2005
19. Söderbäck E, Zackrisson AL, Lindblom B, Alderborn A. Determination of
CYP2D6 gene copy number by pyrosequencing. Clin Chem 2005;51:522-31.
20. Malmström H, Storå J, Dalén L, Holmlund G, Götherström A. Extensive
human DNA contamination in extracts from ancient dog bones and teeth. Mol
Biol Evol 2005;22:2040-7.
2006
21. Kindberg E, Hejdeman B, Bratt G, Wahren B, Lindblom B, Hinkula J,
Svensson L. A nonsense mutation (428G-->A) in the fucosyltransferase
FUT2 gene affects the progression of HIV-1 infection. AIDS 2006;20:685-9.
22. Holmlund G, Nilsson H, Karlsson A, Lindblom B. Y-chromosome STR
haplotypes in Sweden. Forensic Sci Int 2006;160:66-79.
23. Karlsson AO, Wallerström T, Götherström A, Holmlund G. Y-chromosome
diversity in Sweden - a long-time perspective. Eur J Hum Genet 2006;14:96370.
2007
24. Malmström H, Svensson EM, Gilbert MT, Willerslev E, Götherström A,
Holmlund G. More on contamination: the use of asymmetric molecular
behavior to identify authentic ancient human DNA. Mol Biol Evol
2007;24:998-1004.
25. Karlsson AO, Holmlund G, Egeland T, Mostad P. DNA-testing for
immigration cases: the risk of erroneous conclusions. Forensic Sci Int
2007;172:144-9.
26. Karlsson AO, Holmlund G. Identification of mammal species using speciesspecific DNA pyrosequencing. Forensic Sci Int 2007;173:16-20.
2008
27. Holmlund G, Wetterling G, Formisto T, Kauppila R. Identification, of four
crewmembers of the Douglas DC-3 79001 Hugin by DNA analysis, 52 years
post mortem. Scand J of Forensic Science 2008;14:5-9.
28. Malmström H, Vilà C, Gilbert MT, Storå J, Willerslev E, Holmlund G,
Götherström A. Barking up the wrong tree: modern northern European dogs
fail to explain their origin. BMC Evol Biol 2008;8:71
29. Linderholm A, Malmström H, Lidén K, Holmlund G, Götherström A. Cryptic
contamination and phylogenetic nonsense. PLoS One 2008;3(5):e2316.
30. Montelius K, Karlsson AO, Holmlund G. STR data for the AmpFlSTR
Identifiler loci from Swedish population in comparison to European, as well
as with non-European population. Forensic Sci Int Genet 2008;2(3):e49-52.
31. Lao O, Lu TT, Nothnagel M, Junge O, Freitag-Wolf S, Caliebe A,
Balascakova M, Bertranpetit J, Bindoff LA, Comas D, Holmlund G, Kouvatsi
A, Macek M, Mollet I, Parson W, Palo J, Ploski R, Sajantila A, Tagliabracci
A, Gether U, Werge T, Rivadeneira F, Hofman A, Uitterlinden AG, Gieger C,
Wichmann HE, Rüther A,Schreiber S, Becker C, Nürnberg P, Nelson MR,
Krawczak M, Kayser M. Correlation between genetic and geographic
structure in Europe. Curr Biol 2008;18:1241-8.
32. Tillmar AO, Mostad P, Egeland T, Lindblom B, Holmlund G, Montelius K.
Analysis of linkage and linkage disequilibrium for eight X-STR markers.
Forensic Sci Int Genet 2008;3:37-41.
33. Perskvist N(1), Skoglund K, Edston E, Bäckström G, Lodestad I, Palm U.
Fetal TNF-alpha and IL-10 gene polymorphisms versus cardioimmunological
responses in sudden infant death. Pediatr Pathol. 2008;27:149-6.
2009
34. Lu TT, Lao O, Nothnagel M, Junge O, Freitag-Wolf S, Caliebe A,
Balascakova M, Bertranpetit J, Bindoff LA, Comas D, Holmlund G, Kouvatsi
A, Macek M, Mollet I, Nielsen F, Parson W, Palo J, Ploski R, Sajantila A,
Tagliabracci A, Gether U, Werge T, Rivadeneira F, Hofman A, Uitterlinden
AG, Gieger C, Wichmann HE, RuetherA, Schreiber S, Becker C, Nürnberg P,
Nelson MR, Kayser M, Krawczak M. An evaluation of the genetic-matched
pair study design using genome-wide SNP data from the European
population. Eur J Hum Gene. 2009;17:967-75.
35. Malmström H, Gilbert MT, Thomas MG, Brandström M, Storå J, Molnar P,
Andersen PK, Bendixen C, Holmlund G, Götherström A, Willerslev E.
Ancient DNA reveals lack of continuity between neolithic hunter-gatherers
and contemporary Scandinavians. Curr Biol 2009;19:1758-62.
36. Tillmar AO, Bäckström G, Montelius K. Genetic variation of 15 autosomal
STR loci in a Somali population 1. Forensic Sci Int Genet 2009;4(1):e19-20.
37. Helena Malmström, M. Thomas P. Gilbert, Mark G. Thomas, Mikael
Brandström, Jan Storå, Petra Molnar, Pernille K. Andersen, Christian
Bendixen, Gunilla Holmlund, Anders Götherström, Eske Willerslev. Ancient
DNA reveals lack of continuity between Neolithic Hunter-Gatherers and
contemporary Scandinavians. Current Biology 2009.09.017.
2010
38. Tillmar AO, Coble MD, Wallerström T, Holmlund G. Homogeneity in
mitochondrial DNA control region sequences in Swedish subpopulations. Int
J Legal Med 2010;124:91-8.
39. Malmström H, Linderholm A, Lidén K, Storå J, Molnar P, Holmlund G,
Jakobsson M, Götherström A. High frequency of lactose intolerance in a
prehistoric hunter-gatherer population in northern Europe. BMC Evol Biol.
2010;10:89.
40. Winskog C , Nilsson H, Montelius K, Lindblom B The use of commercial
alcohol products to sterilize bones prior to DNA sampling. Forensic Sci Med
Pathol. 2010 Jun;6(2):127-9.
41. Ahlner J, Zackrisson AL, Lindblom B, Bertilsson L CYP2D6, serotonin and
suicide. Pharmacogenomics 2010;11:903-5.
2011
42. Zackrisson AL, Lindblom B, Ahlner J.High frequency of occurrence of
CYP2D6 gene duplication/multiduplication indicating ultrarapid metabolism
among suicide cases. 24. Clin Pharmacol Ther. 2010 Sep;88(3):354-9.
Comment in Clin Pharmacol Ther. 2011 Mar;89(3):352-3. Clin Pharmacol
Ther 2010;88:304-5.
43. Tomas C, Axler-DiPerte G, Budimlija ZM, Børsting C, Coble MD, Decker
AE,Eisenberg A, Fang R, Fondevila M, Fredslund SF, Gonzalez S, Hansen
AJ, Hoff-Olsen P, Haas C, Kohler P, Kriegel AK, Lindblom B, Manohar F,
Maroñas O, Mogensen HS,Neureuther K, Nilsson H, Scheible MK, Schneider
PM, Sonntag ML, Stangegaard M,Syndercombe-Court D, Thacker CR,
Vallone PM, Westen AA, Morling N.Autosomal SNP typing of forensic
samples with the GenPlex™ HID System: results ofa collaborative study. 15.
Forensic Sci Int Genet 2011;5:369-75.
44. Tillmar AO, Egeland T, Lindblom B, Holmlund G, Mostad P. Using Xchromosomal markers in relationship testing: calculation of likelihood ratios
taking both linkage and linkage disequilibrium into account. Forensic Sci Int
Genet 2011;5:506-11.
45.
Tillmar AO. Population genetic analysis of 12 X-STRs in Swedish
population. Forensic Sci Int Genet 2011;6:e80-e81.
46. Egeland T, Dawid AP, Mortera J, Mostad P, Tillmar A. Response to: DNA
identification by pedigree likelihood ratio accommodating population
substructure and mutations. Investig Genet 2011;2:7.
2012
47. Malmström H, Vretemark M, Tillmar A, Durling MB, Skoglund P, Gilbert
MT, Willerslev E, Holmlund G, Götherström A. Finding the founder of
Stockholm – a kinship study based on Y-chromosomal, autosomal and
mitochondrial DNA. Ann Anat 2012;194:138-45.
48. Kingbäck M, Karlsson L, Zackrisson AL, Carlsson B, Josefsson M,
Bengtsson F, Ahlner J, Kugelberg FC. Influence of CYP2D6 genotype on the
disposition of the.enantiomers of venlafaxine and its major metabolites in
postmortem femoral blood. Forensic Sci Int 2012;214:124-34.
49. Kling D, Welander J, Tillmar A, Skare O, Egeland T, Holmlund G. DNA
microarray as a tool in establishing genetic relatedness--Current status and
future prospects. Forensic Sci Int Gene. 2012;6:322-9.
50. Kling D, Egeland T, Tillmar AO. FamLink--a user friendly software for
linkage calculations in family genetics. Forensic Sci Int Genet 2012;6:616-20.
51. O'Connor KL, Tillmar AO. Effect of linkage between vWA and D12S391 in
kinship analysis. Forensic Sci Int Genet 2012;6:840-4.
2013
52. Tillmar AO, Nilsson H, Kling D, Montelius K. Analysis of Investigator
Hdplex markers in Swedish and Somali populations. Forensic Sci Int Genet.
2013;7:e21-2.
53. Montelius K, Lindblom B. DNA analysis in Disaster Victim Identification.
Forensic Sci Med Pathol 2012;8:140-7.
54. Alkass K, Saitoh H, Buchholz BA, Bernard S, Holmlund G, Senn DR,
Spalding KL, Druid H. Analysis of radiocarbon, stable isotopes and DNA in
teeth to facilitate identification of unknown decedents. PLoS One
2013;29;8:e69597.
55. Tillmar AO, Dell’Amico B, Welander J, Holmlund G. A universal method for
species identification of mammals utilizing next generation sequencing for
the analysis of DNA mixtures. PloS One 2013;8:e83761.
Proceedings
56. Holmlund G, Lindblom B. Evaluation of variable number of tandem repeat
(VNTR) alleles in mother-child combinations, 1990. In: DNA-Technology
and Its Forensic Application. Edited by Berghaus, Brinkman, Rittner, Staak.
Springer-Verlag Berlin Heidelberg 1991 pp 116-20.
57. Wetterling G. Intragenic recombination within the Apha-1-Antitrypsin locus.
In Avances in Forensic Haemogenetics 4. Edited by CH Rittner, PM
Schnider. Springer-Verlag Berlin Heidielberg 1992 pp 317-9.
58. Holmlund G, Lodestad I, Engdahl L, Langö A, Ekdal A-m, Sandehed M,
Malmgred H, Nordlöf S, Bäckström G, Berkowicz A, Lindblom B. Analysis
of highly degraded DNA by solid phase cycle sequencing of class II alleles
for forensic applications. In: Progress in Forensic Genetics 7. Edited by
Olaisen B, Brinkman B and Lincoln PJ. Elsevier Science 1998 pp 177-79.
59. Holmlund G, Engdahl L, Marttila M, Lindblom B. Allelic diversity in the
variable number of tandem repeat markar D2S44 (YNH24) as shown by
multivariant repeat mapping. In: Progress in Forensic Genetics 7. Edited by
Olaisen B, Brinkman B and Lincoln PJ. Elsevier Science 1998 pp 234-6.
60. Malmgren H, Langö L, Holmlund G, Engdahl L, Nordlöf S, Lindblom B.
DAN-sequencing of an allelic ladder comprising AAAG repeats and inter-gel
variation of allele sizes. In: Progress in Forensic Genetics 7. Edited by
Olaisen B, Brinkman B and Lincoln PJ. Elsevier Science 1998 pp 481-3.
61. Holmlund G, Nilsson H, Engdahl L, Göterhström A, Linblom B. No obvious
geographical Y-Chromosome gradient in the Swedish population. In:
Progress in Forensic Genetics 10. Edited by C Doutremépuichand N Morling.
International Congress Series, Elsevier 1216 2004 pp 357-9.
62. Karlsson AO, Götherström A, Wallerström T, and Holmlund G. YChromosome variation in Swedish, Saami and Österbotten male lineages. In:
Progress in Forensic Genetics II. Edited by A Amorim, F Corte-Real and N
Morling. International Congress Series 1288, 2006 pp 240-2.
63. Holmlund G, Lodestad I, Nilsson H, Lindblom B. Experiences from the ante
mortem and post mortem DNA-analysis in Sweden for the identification of
tsunami victims. In Progress in Forensic Genetics II. Edited by A Amorim, F
Corte-Real and N Morling International Congress Series 1288 , 2006 pp 7446.
Bokkapitel
Holmlund G. Ikaros, Flygvapenmusei årsbok 2009. Identifiering med DNAteknik. ISSN 1102-1926. AB Danagårds Grafiska 2010 pp 52-6
2014
64. Ballantyne KN, Ralf A, Aboukhalid R, Achakzai NM, Anjos MJ, Ayub Q,
Balažic J, Ballantyne J, Ballard DJ, Berger B, Bobillo C, Bouabdellah M,
Burri H, Capal T, Caratti S, Cárdenas J, Cartault F, Carvalho EF, Carvalho
M, Cheng B, Coble MD, Comas D, Corach D, D'Amato ME, Davison S, de
Knijff P, De Ungria MC, Decorte R, Dobosz T, Dupuy BM, Elmrghni S,
Gliwiński M, Gomes SC, Grol L, Haas C, Hanson E, Henke J, Henke L,
Herrera-Rodríguez F, Hill CR, Holmlund G, Honda K, Immel UD, Inokuchi
S, Jobling MA, Kaddura M, Kim JS, Kim SH, Kim W, King TE,
Klausriegler E, Kling D, Kovačević L, Kovatsi L, Krajewski P, Kravchenko
S, Larmuseau MH, Lee EY, Lessig R, Livshits LA, Marjanović D, Minarik
M, Mizuno N, Moreira H, Morling N, Mukherjee M, Munier P, Nagaraju J,
Neuhuber F, Nie S, Nilasitsataporn P, Nishi T, Oh HH, Olofsson J, Onofri
V, Palo JU, Pamjav H, Parson W, Petlach M, Phillips C, Ploski R, Prasad
SP, Primorac D, Purnomo GA, Purps J, Rangel-Villalobos H, Rębała K,
Rerkamnuaychoke B, Gonzalez DR, Robino C, Roewer L, Rosa A, Sajantila
A, Sala A, Salvador JM, Sanz P, Schmitt C, Sharma AK, Silva DA, Shin KJ,
Sijen T Sirker M, Siváková D, Skaro V, Solano-Matamoros C, Souto L,
Stenzl V, Sudoyo H, Syndercombe-Court D, Tagliabracci A, Taylor D,
Tillmar A, Tsybovsky IS, Tyler-Smith C, van der Gaag KJ, Vanek D, Völgyi
A, Ward D, Willemse P, Yap EP, Yong RY, Pajnič IZ, Kayser M. Toward
male individualization with rapidly mutating y-chromosomal short tandem
repeats. Hum Mutat. 2014;35(8):1021-32.
65. Bastami S, Gupta A, Zackrisson AL, Ahlner J, Osman A, Uppugunduri S.
Influence of UGT2B7, OPRM1 and ABCB1 Gene Polymorphisms on
Postoperative Morphine Consumption. Basic Clin Pharmacol Toxicol. 2014
April. doi10.1111bcpt12248. Epub. 2014 May 19.
66. Bastami S, Haage P, Kronstrand R, Kugelberg FC, Zackrisson AL,
Uppugunduri S. Pharmacogenetic aspects of tramadol pharmacokinetics and
pharmacodynamics after a single oral dose. Forensic Sci Int. 2014;238:12532.
67. Chaitanya L, Walsh S, Andersen JD, Ansell R, Ballantyne K, Ballard D,
Banemann R, Bauer CM, Bento AM, Brisighelli F, Capal T, Clarisse L,
Gross TE, Haas C, Hoff-Olsen P, Hollard C, Keyser C, Kiesler KM, Kohler
P, Kupiec T, Linacre A, Minawi A, Morling N, Nilsson H, Norén L, Ottens
R, Palo JU, Parson W, Pascali VL, Phillips C, Porto MJ, Sajantila A,
Schneider PM, Sijen T, Söchtig J, Syndercombe-Court D, Tillmar A,
Turanska M, Vallone PM, Zatkalíková L, Zidkova A, Branicki W, Kayser
M. Collaborative EDNAP exercise on the IrisPlex system for DNA-based
prediction of human eye colour. Forensic Sci Int Genet. 2014 Jul;11:241-51.
doi: 10.1016/j.fsigen.2014.04.006. Epub 2014 Apr 21.
68. Hasmats J, Gréen H, Orear C, Validire P, Huss M, Max Käller M,
Lundeberg J. Assessment of whole genome amplification for sequence
capture and massive parallel sequencing. PLoS One 2014;9(1):e84785
69. Jakobsen Falk I, Fyrberg A, Paul E, Nahi H, Hermanson M, Rosenquist R,
Höglund M, Palmqvist L, Stockelberg D, Wei Y, Gréen H, Lotfi K. Impact
of ABCB1 single nucleotide polymorphisms 1236C>T and 2677G>T on
overall survival in FLT3 wild-type de novo AML patients with normal
karyotype. British Journal of Haematology 2014 Dec;167(5):671-80. doi:
10.1111/bjh.13097.
70. Jakobsen Falk I, Kerstin K, Chaireti R, Lund J, Nahi H, Hermanson M,
Gréen H Lotfi K, Söderkvist P. TP53 mutations and Mdm2SNP309 identify
subgroups of AML patients with impaired outcome. European Journal of
Haematology 2014 Aug 23. doi: 10.1111/ejh.12438.
71. Karlsson L, Zackrisson AL, Josefsson M, Carlsson B, Green H, Kugelberg
FC Influence of CYP2D6 and CYP2C19 genotypes on venlafaxine
metabolic ratios and stereoselective metabolism in forensic autopsy cases.
Pharmacogenomics J. 2014. doi: 10.1038/tpj.2014.50. Epub 2014 Sept 23.
72. Khan MS, Zetterlund EL, Gréen H, Oscarsson A, Zackrisson AL, Svanborg
E, Lindholm ML, Persson H, Eintrei C. Pharmacogenetics, plasma
concentrations, clinical signs and EEG during propofol treatment. Basic Clin
Pharmacol Toxicol. 2014;115(6):565-70.
73. Kling D, Dell'Amico B, Haddeland PJ, Tillmar AO. Population genetic
analysis of 12 X-STRs in a Somali population sample. Forensic Sci Int
Genet. 2014;11:e7-8.
74. Kling D, Tillmar A, Egeland T, Mostad P. A general model for likelihood
computations of genetic marker data accounting for linkage, linkage
disequilibrium, and mutations. Int J Legal Med. 2014. Doi: 10.1007/s00414014-1117-7. Epub. 2014 Nov 26.
75. Montelius K, Stenersen M, Sajantila A. Genetic Profiling in Disaster Victim
Identification. eLS July 2014, John Wiley & Sons, Ltd: Chichester DOI:
10.1002/9780470015902.a0024394
76. Purps J, Siegert S, Willuweit S, Nagy M, Alves C, Salazar R, Angustia SM,
Santos LH, Anslinger K, Bayer B, Ayub Q, Wei W, Xue Y, Tyler-Smith C,
Bafalluy MB, Martínez-Jarreta B, Egyed B, Balitzki B, Tschumi S, Ballard
D, Court DS, Barrantes X, Bäßler G, Wiest T, Berger B, Niederstätter H,
Parson W, Davis C, Budowle B, Burri H, Borer U, Koller C, Carvalho EF,
Domingues PM, Chamoun WT, Coble MD, Hill CR, Corach D, Caputo M,
D'Amato ME, Davison S, Decorte R Larmuseau MH, Ottoni C, Rickards O,
Lu D, Jiang C, Dobosz T, Jonkisz A, Frank WE, Furac I, Gehrig C, Castella
V, Grskovic B, Haas C, Wobst J, Hadzic G, Drobnic K, Honda K, Hou Y,
Zhou D, Li Y, Hu S, Chen S, Immel UD, Lessig R, Jakovski Z, Ilievska T,
Klann AE, García CC, de Knijff P, Kraaijenbrink T, Kondili A, Miniati P,
Vouropoulou M, Kovacevic L, Marjanovic D, Lindner I, Mansour I, AlAzem M, Andari AE, Marino M, Furfuro S, Locarno L, Martín P, Luque
GM, Alonso A, Miranda LS, Moreira H, Mizuno N, Iwashima Y, Neto RS,
Nogueira TL, Silva R, Nastainczyk-Wulf M, Edelmann J, Kohl M, Nie S,
Wang X, Cheng B, Núñez C, Pancorbo MM, Olofsson JK, Morling N,
Onofri V, Tagliabracci A, Pamjav H, Volgyi A, Barany G, Pawlowski R,
Maciejewska A, Pelotti S, Pepinski W, Abreu-Glowacka M, Phillips C,
Cárdenas J, Rey-Gonzalez D, Salas A, Brisighelli F, Capelli C, Toscanini U,
Piccinini A, Piglionica M, Baldassarra SL, Ploski R, Konarzewska M,
Jastrzebska E, Robino C, Sajantila A, Palo JU, Guevara E, Salvador J,
Ungria MC, Rodriguez JJ, Schmidt U, Schlauderer N, Saukko P, Schneider
PM, Sirker M, Shin KJ, Oh YN, Skitsa I, Ampati A, Smith TG, Calvit LS,
Stenzl V, Capal T, Tillmar A, Nilsson H, Turrina S, De Leo D, Verzeletti A,
Cortellini V, Wetton JH, Gwynne GM, Jobling MA, Whittle MR, Sumita
DR, Wolańska-Nowak P, Yong RY, Krawczak M, Nothnagel M, Roewer L.
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci.
Forensic Sci Int Genet. 2014 Sep;12:12-23. doi:
10.1016/j.fsigen.2014.04.008. Epub 2014 Apr 28.
77. Skoglund K, Boiso Moreno S, Jönsson J-I, Vikingsson S, Carlsson B, Gréen
H. Single-nucleotide polymorphisms of ABCG2 increase the efficacy of
tyrosine kinase inhibitors in the K562 chronic myeloid leukemia cell line.
Pharmacogenetics and Genomics 2014 Jan;24(1):52-61.
78. Tillmar AO, Mostad P. Choosing supplementary markers in forensic
casework. Forensic Sci Int Genet. 2014;13:128-33. Kling D, Tillmar AO,
Egeland T. Familias 3 - Extensions and new functionality. Forensic Sci Int
Genet. 2014;13:121-7.
79. Willander K, Jakobsen Falk I, Chaireti R, Paul E, Hermanson M, Gréen H,
Lotfi K, Söderkvist P. Mutations in the isocitrate dehydrogenase 1/2 genes
and IDH1 SNP 105C>T have a prognostic value in acute myeloid leukemia.
Biomarker Research 2014, 2:18.
80. Zetterlund E-L, Suleman Khan M, Gréen H, Zackrisson A-L, Ottosson A,
Eintrei C. Pharmacogenetics, Plasma Concentrations, Clinical Signs and
EEG during Propofol Treatment. Basic and Clinical Toxicology and
Pharmacology 2014 Dec;115(6):565-70. doi: 10.1111/bcpt.12277.
81. Ballantyne KN, Ralf A, Aboukhalid R, Achakzai NM, Anjos MJ, Ayub Q,
Balažic J, Ballantyne J, Ballard DJ, Berger B, Bobillo C, Bouabdellah M,
Burri H, Capal T, Caratti S, Cárdenas J, Cartault F, Carvalho EF, Carvalho
M, Cheng B, Coble MD, Comas D, Corach D, D'Amato ME, Davison S, de
Knijff P, De Ungria MC, Decorte R, Dobosz T, Dupuy BM, Elmrghni S,
Gliwiński M, Gomes SC, Grol L, Haas C, Hanson E, Henke J, Henke L,
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