Axel Hillmer
Axel Hillmer
Institute of Pathology, University Hospital Cologne
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Cited by
Cited by
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
A Ramirez, A Heimbach, J Gründemann, B Stiller, D Hampshire, LP Cid, ...
Nature genetics 38 (10), 1184-1191, 2006
Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes
ZJ Zang, I Cutcutache, SL Poon, SL Zhang, JR McPherson, J Tao, ...
Nature genetics 44 (5), 570-574, 2012
A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer
KP Ng, AM Hillmer, CTH Chuah, WC Juan, TK Ko, ASM Teo, ...
Nature medicine 18 (4), 521, 2012
G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth
SM Pasternack, I von Kügelgen, K Al Aboud, YA Lee, F Rüschendorf, ...
Nature genetics 40 (3), 329-334, 2008
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia
J Schumacher, H Anthoni, F Dahdouh, IR König, AM Hillmer, N Kluck, ...
The American Journal of Human Genetics 78 (1), 52-62, 2006
Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors
H Li, ET Courtois, D Sengupta, Y Tan, KH Chen, JJL Goh, SL Kong, ...
Nature genetics 49 (5), 708-718, 2017
Bystander CD8+ T cells are abundant and phenotypically distinct in human tumour infiltrates
Y Simoni, E Becht, M Fehlings, CY Loh, SL Koo, KWW Teng, JPS Yeong, ...
Nature 557 (7706), 575-579, 2018
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
AM Hillmer, S Hanneken, S Ritzmann, T Becker, J Freudenberg, ...
The American Journal of Human Genetics 77 (1), 140-148, 2005
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
R Abraham, V Moskvina, R Sims, P Hollingworth, A Morgan, L Georgieva, ...
BMC medical genomics 1 (1), 44, 2008
A genome-wide association study in 574 schizophrenia trios using DNA pooling
G Kirov, I Zaharieva, L Georgieva, V Moskvina, I Nikolov, S Cichon, ...
Molecular psychiatry 14 (8), 796-803, 2009
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin
E Levy-Nissenbaum, RC Betz, M Frydman, M Simon, H Lahat, T Bakhan, ...
Nature genetics 34 (2), 151-153, 2003
Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia
S Cichon, M Anker, IR Vogt, H Rohleder, M Pützstück, A Hillmer, ...
Human molecular genetics 7 (11), 1671-1679, 1998
Susceptibility variants for male-pattern baldness on chromosome 20p11
AM Hillmer, FF Brockschmidt, S Hanneken, S Eigelshoven, M Steffens, ...
Nature genetics 40 (11), 1279-1281, 2008
Whole-genome reconstruction and mutational signatures in gastric cancer
N Nagarajan, D Bertrand, AM Hillmer, ZJ Zang, F Yao, PÉ Jacques, ...
Genome biology 13 (12), 1-10, 2012
Novel therapeutic targets on the horizon for lung cancer
WL Tan, A Jain, A Takano, EW Newell, NG Iyer, WT Lim, EH Tan, W Zhai, ...
The Lancet Oncology 17 (8), e347-e362, 2016
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European …
J Schumacher, G Laje, RA Jamra, T Becker, TW Mühleisen, C Vasilescu, ...
Human molecular genetics 18 (14), 2719-2727, 2009
Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes
AM Hillmer, F Yao, K Inaki, WH Lee, PN Ariyaratne, ASM Teo, XY Woo, ...
Genome research 21 (5), 665-675, 2011
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease
RC Betz, J Pforr, A Flaquer, S Redler, S Hanneken, S Eigelshoven, ...
Journal of Investigative Dermatology 127 (11), 2539-2543, 2007
Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26
AM Hillmer, A Flaquer, S Hanneken, S Eigelshoven, AK Kortüm, ...
The American Journal of Human Genetics 82 (3), 737-743, 2008
Transcriptional consequences of genomic structural aberrations in breast cancer
K Inaki, AM Hillmer, L Ukil, F Yao, XY Woo, LA Vardy, KFB Zawack, ...
Genome research 21 (5), 676-687, 2011
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