Martin Kircher
Martin Kircher
Berlin Institute of Health, Charité - Universitätsmedizin Berlin
Verified email at - Homepage
Cited by
Cited by
A general framework for estimating the relative pathogenicity of human genetic variants
M Kircher, DM Witten, P Jain, BJ O'roak, GM Cooper, J Shendure
Nature genetics 46 (3), 310-315, 2014
A draft sequence of the Neandertal genome
RE Green, J Krause, AW Briggs, T Maricic, U Stenzel, M Kircher, ...
science 328 (5979), 710-722, 2010
CADD: predicting the deleteriousness of variants throughout the human genome
P Rentzsch, D Witten, GM Cooper, J Shendure, M Kircher
Nucleic acids research 47 (D1), D886-D894, 2019
The complete genome sequence of a Neanderthal from the Altai Mountains
K Prüfer, F Racimo, N Patterson, F Jay, S Sankararaman, S Sawyer, ...
Nature 505 (7481), 43-49, 2014
Illumina sequencing library preparation for highly multiplexed target capture and sequencing
M Meyer, M Kircher
Cold Spring Harbor Protocols 2010 (6), pdb. prot5448, 2010
Genetic history of an archaic hominin group from Denisova Cave in Siberia
D Reich, RE Green, M Kircher, J Krause, N Patterson, EY Durand, B Viola, ...
Nature 468 (7327), 1053-1060, 2010
A high-coverage genome sequence from an archaic Denisovan individual
M Meyer, M Kircher, MT Gansauge, H Li, F Racimo, S Mallick, ...
Science 338 (6104), 222-226, 2012
Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin
MW Snyder, M Kircher, AJ Hill, RM Daza, J Shendure
Cell 164 (1), 57-68, 2016
The evolution of gene expression levels in mammalian organs
D Brawand, M Soumillon, A Necsulea, P Julien, G Csárdi, P Harrigan, ...
Nature 478 (7369), 343-348, 2011
Deep proteome and transcriptome mapping of a human cancer cell line
N Nagaraj, JR Wisniewski, T Geiger, J Cox, M Kircher, J Kelso, S Pääbo, ...
Molecular systems biology 7 (1), 548, 2011
Double indexing overcomes inaccuracies in multiplex sequencing on the Illumina platform
M Kircher, S Sawyer, M Meyer
Nucleic acids research 40 (1), e3-e3, 2012
High‐throughput DNA sequencing–concepts and limitations
M Kircher, J Kelso
Bioessays 32 (6), 524-536, 2010
Denisova admixture and the first modern human dispersals into Southeast Asia and Oceania
D Reich, N Patterson, M Kircher, F Delfin, MR Nandineni, I Pugach, ...
The American Journal of Human Genetics 89 (4), 516-528, 2011
The genetic basis of Mendelian phenotypes: discoveries, challenges, and opportunities
JX Chong, KJ Buckingham, SN Jhangiani, C Boehm, N Sobreira, ...
The American Journal of Human Genetics 97 (2), 199-215, 2015
Ancient gene flow from early modern humans into Eastern Neanderthals
M Kuhlwilm, I Gronau, MJ Hubisz, C De Filippo, J Prado-Martinez, ...
Nature 530 (7591), 429-433, 2016
Characterization of ancient and modern genomes by SNP detection and phylogenomic and metagenomic analysis using PALEOMIX
M Schubert, L Ermini, CD Sarkissian, H Jónsson, A Ginolhac, R Schaefer, ...
Nature protocols 9 (5), 1056-1082, 2014
Removal of deaminated cytosines and detection of in vivo methylation in ancient DNA
AW Briggs, U Stenzel, M Meyer, J Krause, M Kircher, S Pääbo
Nucleic acids research 38 (6), e87-e87, 2010
CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores
P Rentzsch, M Schubach, J Shendure, M Kircher
Genome medicine 13, 1-12, 2021
Improved base calling for the Illumina Genome Analyzer using machine learning strategies
M Kircher, U Stenzel, J Kelso
Genome biology 10, 1-9, 2009
Multiplex assessment of protein variant abundance by massively parallel sequencing
KA Matreyek, LM Starita, JJ Stephany, B Martin, MA Chiasson, VE Gray, ...
Nature genetics 50 (6), 874-882, 2018
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