Axel M. Hillmer

Overview

Best Publications

• Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.

  Alfredo Ramirez;André Heimbach;Jan Gründemann;Barbara Stiller

  1363
  Citations

• Bystander CD8+ T cells are abundant and phenotypically distinct in human tumour infiltrates

  Yannick Simoni;Etienne Becht;Michael Fehlings;Chiew Yee Loh

  1360
  Citations

• Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors

  Huipeng Li;Elise T Courtois;Debarka Sengupta;Debarka Sengupta;Yuliana Tan

  961
  Citations

• Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes

  Zhi Jiang Zang;Ioana Cutcutache;Song Ling Poon;Shen Li Zhang

  696
  Citations

• A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer.

  King Pan Ng;Axel M Hillmer;Charles T H Chuah;Charles T H Chuah;Wen Chun Juan

  681
  Citations

• G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.

  Sandra M Pasternack;Ivar von Kügelgen;Khalid Al Aboud;Young-Ae Lee;Young-Ae Lee

  468
  Citations

• Genomic landscape of lung adenocarcinoma in East Asians

  Jianbin Chen;Hechuan Yang;Hechuan Yang;Audrey Su Min Teo;Lidyana Bte Amer

  373
  Citations

• Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia

  Johannes Schumacher;Heidi Anthoni;Faten Dahdouh;Inke R. König

  347
  Citations

• Methionine is a metabolic dependency of tumor-initiating cells.

  Zhenxun Wang;Lian Yee Yip;Jia Hui Jane Lee;Jia Hui Jane Lee;Zhengwei Wu;Zhengwei Wu

  311
  Citations

• Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia

  Axel M. Hillmer;Sandra Hanneken;Sibylle Ritzmann;Tim Becker

  275
  Citations

• A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

  Richard Abraham;Valentina Moskvina;Rebecca Sims;Paul Hollingworth

  228
  Citations

• A genome-wide association study in 574 schizophrenia trios using DNA pooling

  G Kirov;I Zaharieva;L Georgieva;Moskvina

  216
  Citations

• Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

  Etgar Levy-Nissenbaum;Regina C Betz;Moshe Frydman;Michel Simon

  212
  Citations

• Novel therapeutic targets on the horizon for lung cancer.

  Wan-Ling Tan;Amit Jain;Angela Takano;Evan W Newell

  194
  Citations

• Cloning, Genomic Organization, Alternative Transcripts and Mutational Analysis of the Gene Responsible for Autosomal Recessive Universal Congenital Alopecia

  Sven Cichon;Martina Anker;Ina R. Vogt;Hendrik Rohleder

  185
  Citations

• Susceptibility variants for male-pattern baldness on chromosome 20p11

  Axel M Hillmer;Felix F Brockschmidt;Sandra Hanneken;Sibylle Eigelshoven

  177
  Citations

• Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing

  Rahul Nahar;Weiwei Zhai;Weiwei Zhai;Tong Zhang;Angela Takano

  151
  Citations

• Recurrent Fusion Genes in Gastric Cancer: CLDN18-ARHGAP26 Induces Loss of Epithelial Integrity

  Fei Yao;Fei Yao;Jaya P. Kausalya;Yee Yen Sia;Yee Yen Sia;Audrey S.M. Teo;Audrey S.M. Teo

  149
  Citations

• Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

  Tin Aung;Tin Aung;Mineo Ozaki;Mei Chin Lee;Ursula Schlötzer-Schrehardt

  146
  Citations

• Whole-genome reconstruction and mutational signatures in gastric cancer

  Niranjan Nagarajan;Denis Bertrand;Axel M Hillmer;Zhi Jiang Zang

  141
  Citations