Axel M Hillmer


Ontology type: schema:Person     


Person Info

NAME

Axel M

SURNAME

Hillmer

Publications in SciGraph latest 50 shown

  • 2018-12 Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing in NATURE COMMUNICATIONS
  • 2018-11-12 Author Correction: Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors in NATURE GENETICS
  • 2018-05 Bystander CD8+ T cells are abundant and phenotypically distinct in human tumour infiltrates in NATURE
  • 2017-12 Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus in NATURE COMMUNICATIONS
  • 2017-07 Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci in NATURE GENETICS
  • 2017-05 Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors in NATURE GENETICS
  • 2017-03-08 Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness in NATURE COMMUNICATIONS
  • 2017-02 De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development in NATURE GENETICS
  • 2016-12 OPTIMA: sensitive and accurate whole-genome alignment of error-prone genomic maps by combinatorial indexing and technology-agnostic statistical analysis in GIGASCIENCE
  • 2016-09-28 Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity in NATURE COMMUNICATIONS
  • 2015-12 Single-molecule optical genome mapping of a human HapMap and a colorectal cancer cell line in GIGASCIENCE
  • 2015-12 High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer in GENOME BIOLOGY
  • 2015-06 Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome in NATURE GENETICS
  • 2015-04 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome in NATURE GENETICS
  • 2014-12 Functional chromatin features are associated with structural mutations in cancer in BMC GENOMICS
  • 2014-10 Reply: The BIM deletion polymorphism cannot account for intrinsic TKI resistance of Chinese individuals with chronic myeloid leukemia in NATURE MEDICINE
  • 2013-06 Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2012-12 Whole-genome reconstruction and mutational signatures in gastric cancer in GENOME BIOLOGY
  • 2012-05 Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes in NATURE GENETICS
  • 2012-04 A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer in NATURE MEDICINE
  • 2012-03 Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-12 Genetik der androgenetischen Alopezie in MEDIZINISCHE GENETIK
  • 2009-08 Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness in HUMAN GENETICS
  • 2009-08 A genome-wide association study in 574 schizophrenia trios using DNA pooling in MOLECULAR PSYCHIATRY
  • 2008-12 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling in BMC MEDICAL GENOMICS
  • 2008-11 Susceptibility variants for male-pattern baldness on chromosome 20p11 in NATURE GENETICS
  • 2008-03 G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth in NATURE GENETICS
  • 2007-11 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 in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2007-09 Genetik der Alopecia areata in MEDIZINISCHE GENETIK
  • 2006-10 Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase in NATURE GENETICS
  • 2003-06 Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin in NATURE GENETICS
  • 1999-12 Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia in JOURNAL OF INVESTIGATIVE DERMATOLOGY
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