Publications 2023

Kulhankova L, Montiel González D, Bindels E, Kling D, Kayser M, Mulugeta E (2023)
Single-cell transcriptome sequencing allows genetic separation, characterization and identification of individuals in multi-person biological mixtures
Commun Biol, 6 (1), 201
DOI 10.1038/s42003-023-04557-z, PubMed 36805025

Mostad P, Tillmar A, Kling D (2023)
Improved computations for relationship inference using low-coverage sequencing data
BMC Bioinformatics, 24 (1), 90
DOI 10.1186/s12859-023-05217-z, PubMed 36894920

Publications 2022

Adolfsson E, Kling D, Gunnarsson C, Jonasson J, Gréen H, Gréen A (2022)
Whole exome sequencing of FFPE samples-expanding the horizon of forensic molecular autopsies
Int J Legal Med, 137 (4), 1215-1234
DOI 10.1007/s00414-022-02906-x, PubMed 36346469

Bergseth EF, Tillmar A, Haddeland PJT, Kling D (2022)
Extended population genetic analysis of 12 X-STRs - Exemplified using a Norwegian population sample
Forensic Sci Int Genet, 60, 102745
DOI 10.1016/j.fsigen.2022.102745, PubMed 35870434

Publications 2021

Adolfsson E, Qvick A, Gréen H, Kling D, Gunnarsson C, Jonasson J, Gréen A (2021)
Technical in-depth comparison of two massive parallel DNA-sequencing methods for formalin-fixed paraffin-embedded tissue from victims of sudden cardiac death
Forensic Sci Int Genet, 53, 102522
DOI 10.1016/j.fsigen.2021.102522, PubMed 33945952

de Vries JH, Kling D, Vidaki A, Arp P, Kalamara V, Verbiest MMPJ, Piniewska-Róg D, Parsons TJ, Uitterlinden AG, Kayser M (2021)
Impact of SNP microarray analysis of compromised DNA on kinship classification success in the context of investigative genetic genealogy
Forensic Sci Int Genet, 56, 102625
DOI 10.1016/j.fsigen.2021.102625, PubMed 34753062

Kling D, Phillips C, Kennett D, Tillmar A (2021)
Investigative genetic genealogy: Current methods, knowledge and practice
Forensic Sci Int Genet, 52, 102474
DOI 10.1016/j.fsigen.2021.102474, PubMed 33592389

Publications 2019

Kling D, Tillmar A (2019)
Forensic genealogy-A comparison of methods to infer distant relationships based on dense SNP data
Forensic Sci Int Genet, 42, 113-124
DOI 10.1016/j.fsigen.2019.06.019, PubMed 31302460

Publications 2018

Kling D (2018)
On the use of dense sets of SNP markers and their potential in relationship inference
Forensic Sci Int Genet, 39, 19-31
DOI 10.1016/j.fsigen.2018.11.022, PubMed 30529859

Publications 2017

Kling D (2017)
Curiosities of X chromosomal markers and haplotypes
Int J Legal Med, 132 (2), 361-371
DOI 10.1007/s00414-017-1612-8, PubMed 28547136

Kling D, Egeland T, Piñero MH, Vigeland MD (2017)
Evaluating the statistical power of DNA-based identification, exemplified by 'The missing grandchildren of Argentina'
Forensic Sci Int Genet, 31, 57-66
DOI 10.1016/j.fsigen.2017.08.006, PubMed 28858673

Kling D, Tillmar A (2017)
Kinship inference for males with identical Y-STR profiles using whole genome SNP data provides a deeper understanding about the level of coancestry in the Swedish male population
Forensic Sci. Int. Genet. Suppl. Ser., 6, E393-E394
DOI 10.1016/j.fsigss.2017.09.165

Tillmar AO, Kling D, Butler JM, Parson W, Prinz M, Schneider PM, Egeland T, Gusmão L (2017)
DNA Commission of the International Society for Forensic Genetics (ISFG): Guidelines on the use of X-STRs in kinship analysis
Forensic Sci Int Genet, 29, 269-275
DOI 10.1016/j.fsigen.2017.05.005, PubMed 28544956

Publications 2016

Kling D, Füredi S (2016)
The successful use of familial searching in six Hungarian high profile cases by applying a new module in Familias 3
Forensic Sci Int Genet, 24, 24-32
DOI 10.1016/j.fsigen.2016.05.012, PubMed 27267559

Tillmar AO, Kling D (2016)
Comments on "Kinship analysis: assessment of related vs unrelated based on defined pedigrees" by S. Turrina et al
Int J Legal Med, 130 (4), 949-951
DOI 10.1007/s00414-016-1316-5, PubMed 26797423

Publications 2015

Dørum G, Kling D, Tillmar A, Vigeland MD, Egeland T (2015)
Mixtures with relatives and linked markers
Int J Legal Med, 130 (3), 621-34
DOI 10.1007/s00414-015-1288-x, PubMed 26614310

Kling D, Dell'Amico B, Tillmar AO (2015)
FamLinkX - implementation of a general model for likelihood computations for X-chromosomal marker data
Forensic Sci Int Genet, 17, 1-7
DOI 10.1016/j.fsigen.2015.02.007, PubMed 25771099

Publications 2014

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 et al. (2014)
Toward male individualization with rapidly mutating y-chromosomal short tandem repeats
Hum Mutat, 35 (8), 1021-32
DOI 10.1002/humu.22599, PubMed 24917567

Dørum G, Kling D, Baeza-Richer C, García-Magariños M, Sæbø S, Desmyter S, Egeland T (2014)
Models and implementation for relationship problems with dropout
Int J Legal Med, 129 (3), 411-23
DOI 10.1007/s00414-014-1046-5, PubMed 25108449

Kling D, Dell'Amico B, Haddeland PJ, Tillmar AO (2014)
Population genetic analysis of 12 X-STRs in a Somali population sample
Forensic Sci Int Genet, 11, e7-8
DOI 10.1016/j.fsigen.2014.02.013, PubMed 24662329

Kling D, Tillmar A, Egeland T, Mostad P (2014)
A general model for likelihood computations of genetic marker data accounting for linkage, linkage disequilibrium, and mutations
Int J Legal Med, 129 (5), 943-54
DOI 10.1007/s00414-014-1117-7, PubMed 25425094

Kling D, Tillmar AO, Egeland T (2014)
Familias 3 - Extensions and new functionality
Forensic Sci Int Genet, 13, 121-7
DOI 10.1016/j.fsigen.2014.07.004, PubMed 25113576

Publications 2013

Dupuy BM, Stenersen M, Kling D (2013)
Frequency data for 35 autosomal STR markers in a Norwegian, an East African, an East Asian and Middle Asian population and simulation of adequate database size
Forensic Sci. Int. Genet. Suppl. Ser., 4 (1), E378-E379
DOI 10.1016/j.fsigss.2014.01.001

Publications 2012

Kling D, Egeland T, Mostad P (2012)
Using object oriented bayesian networks to model linkage, linkage disequilibrium and mutations between STR markers
PLoS One, 7 (9), e43873
DOI 10.1371/journal.pone.0043873, PubMed 22984448

Kling D, Egeland T, Tillmar AO (2012)
FamLink--a user friendly software for linkage calculations in family genetics
Forensic Sci Int Genet, 6 (5), 616-20
DOI 10.1016/j.fsigen.2012.01.012, PubMed 22390853

Tillmar AO, Nilsson H, Kling D, Montelius K (2012)
Analysis of Investigator HDplex markers in Swedish and Somali populations
Forensic Sci Int Genet, 7 (1), e21-2
DOI 10.1016/j.fsigen.2012.08.006, PubMed 22921958

Publications 2011

Kling D, Welander J, Tillmar A, Skare O, Egeland T, Holmlund G (2011)
DNA microarray as a tool in establishing genetic relatedness--Current status and future prospects
Forensic Sci Int Genet, 6 (3), 322-9
DOI 10.1016/j.fsigen.2011.07.007, PubMed 21813350