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H. Surowy · SciRah

Researcher profile · Semantic Scholar

H. Surowy

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H. Surowy — researcher profile on SciRah

h-index: 28
Works: 65
Citations: 6,044

Most-cited papers

Association analysis identifies 65 new breast cancer risk loci
K. Michailidou, S. Lindström, J. Dennis, J. Beesley +355 more
2017Nature1,360 citations Open access
Semantic Scholar
Breast Cancer Risk Genes — Association Analysis in More than 113,000 Women
L. Dorling, S. Carvalho, Jamie Allen, A. González-Neira +193 more
2021New England Journal of Medicine894 citations Open access
Semantic Scholar
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
K. Michailidou, J. Beesley, S. Lindstrom, S. Canisius +239 more
2015Nature Genetics587 citations Open access
Semantic Scholar
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
R. Milne, Karoline B. Kuchenbaecker, K. Michailidou, J. Beesley +466 more
2017Nature Genetics379 citations Open access
Semantic Scholar
RAD51B in Familial Breast Cancer
L. Pelttari, Sofia Khan, Mikko Vuorela, J. Kiiski +93 more
2016PLoS ONE368 citations Open access
Semantic Scholar
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Lang Wu, Wei Shi, J. Long, Xing-Yi Guo +206 more
2018Nature Genetics214 citations Open access
Semantic Scholar
Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers.
M. Schmidt, F. Hogervorst, R. van Hien, S. Cornelissen +80 more
2016Journal of Clinical Oncology184 citations Open access
Semantic Scholar
Plasma DNA integrity as a biomarker for primary and metastatic breast cancer and potential marker for early diagnosis
Dharanija Madhavan, M. Wallwiener, K. Bents, M. Zucknick +10 more
2014Breast Cancer Research and Treatment166 citations
Semantic Scholar
Blood-based DNA methylation as biomarker for breast cancer: a systematic review
Q. Tang, Jie Cheng, Xue Cao, H. Surowy +1 more
2016Clinical Epigenetics156 citations Open access
Semantic Scholar
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization.
Ben Zhang, X. Shu, Ryan J. Delahanty, Chen-Jie Zeng +167 more
2015Journal of the National Cancer Institute126 citations Open access
Semantic Scholar
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
W. Ek, A. Reznichenko, S. Ripke, B. Niesler +40 more
2013Gut121 citations Open access
Semantic Scholar
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
D. Easton, F. Lesueur, B. Decker, K. Michailidou +125 more
2016Journal of Medical Genetics119 citations Open access
Semantic Scholar
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis.
Xiang Shu, Lang Wu, Nikhil K. Khankari, X. Shu +202 more
2018International Journal of Epidemiology103 citations Open access
Semantic Scholar
Plasma miR‐122 and miR‐200 family are prognostic markers in colorectal cancer
M. Maierthaler, A. Benner, M. Hoffmeister, H. Surowy +5 more
2017International Journal of Cancer99 citations Open access
Semantic Scholar
Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms.
M. de la Hoya, O. Soukarieh, Irene López-Perolio, A. Vega +71 more
2016Human Molecular Genetics94 citations Open access
Semantic Scholar
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Dylan M Glubb, M. Maranian, K. Michailidou, K. Pooley +211 more
2015American Journal of Human Genetics93 citations Open access
Semantic Scholar
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
P. Peterlongo, Irene Catucci, M. Colombo, Laura Caleca +92 more
2015Human Molecular Genetics92 citations Open access
Semantic Scholar
Capture and Amplification by Tailing and Switching (CATS)
A. Turchinovich, H. Surowy, A. Serva, M. Zapatka +2 more
2014RNA Biology74 citations Open access
Semantic Scholar
Physical activity, sedentary time and breast cancer risk: A Mendelian randomization study
S. Dixon-Suen, S. Lewis, Richard M. Martin, D. English +154 more
2022British Journal of Sports Medicine66 citations Open access
Semantic Scholar
Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype
N. Bramswig, O. Caluseriu, Hermann-Josef Lüdecke, François Bolduc +7 more
2017Human Genetics62 citations
Semantic Scholar
Circulating free DNA integrity and concentration as independent prognostic markers in metastatic breast cancer
Jie Cheng, T. Holland-Letz, M. Wallwiener, H. Surowy +7 more
2018Breast Cancer Research and Treatment61 citations
Semantic Scholar
Predisposition for TMPRSS2-ERG Fusion in Prostate Cancer by Variants in DNA Repair Genes
Manuel Luedeke, C. Linnert, M. Hofer, H. Surowy +6 more
2009Cancer Epidemiology, Biomarkers and Prevention57 citations
Semantic Scholar
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
L. Dorling, S. Carvalho, Jamie Allen, M. Parsons +102 more
2021medRxiv54 citations Open access
Semantic Scholar
Heritability of baseline and induced micronucleus frequencies.
H. Surowy, A. Rinckleb, Manuel Luedeke, Madeleine Stuber +5 more
2011Mutagenesis44 citations
Semantic Scholar
Cell-free circulating DNA integrity is an independent predictor of impending breast cancer recurrence
Jie Cheng, K. Ćuk, J. Heil, M. Golatta +5 more
2017OncoTarget37 citations Open access
Semantic Scholar
DNA methylation array analysis identifies breast cancer associated RPTOR, MGRN1 and RAPSN hypomethylation in peripheral blood DNA
Q. Tang, T. Holland-Letz, A. Slynko, K. Ćuk +17 more
2016OncoTarget36 citations Open access
Semantic Scholar
Germline mutations of the MSR1 gene in prostate cancer families from Germany
C. Maier, Z. Vesovic, Natascha Bachmann, K. Herkommer +5 more
2006Human Mutation32 citations Open access
Semantic Scholar
Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies
E. Denisova, D. Westphal, H. Surowy, F. Meier +9 more
2021Cancer Gene Therapy28 citations Open access
Semantic Scholar
High tumour mutational burden and EGFR/MAPK pathway activation are therapeutic targets in metastatic porocarcinoma *
D. Westphal, M. Garzarolli, M. Sergon, P. Horák +17 more
2021British Journal of Dermatology28 citations Open access
Semantic Scholar
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
H. Darabi, J. Beesley, Arnaud Droit, S. Kar +110 more
2016Scientific Reports28 citations Open access
Semantic Scholar
Gene expression profiling in aggressive digital papillary adenocarcinoma sheds light on the architecture of a rare sweat gland carcinoma
H. Surowy, A. Giesen, J. Otte, R. Buttner +11 more
2019British Journal of Dermatology27 citations
Semantic Scholar
MCM3AP and POMP Mutations Cause a DNA‐Repair and DNA‐Damage‐Signaling Defect in an Immunodeficient Child
S. Gatz, Daniela Salles, Eva Jacobsen, T. Dörk +14 more
2016Human Mutation23 citations
Semantic Scholar
Profound inhibition of CD73-dependent formation of anti-inflammatory adenosine in B cells of SLE patients
J. Hesse, M. Siekierka-Harreis, B. Steckel, C. Alter +10 more
2021EBioMedicine22 citations Open access
Semantic Scholar
C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation.
E. Lausberg, Sebastian Giesselmann, J. Dewulf, Elsa Wiame +30 more
2021Journal of Clinical Investigation18 citations Open access
Semantic Scholar
The Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms (rs3063368, rs755622) Predict Acute Kidney Injury and Death after Cardiac Surgery
Luisa Averdunk, J. Bernhagen, K. Fehnle, H. Surowy +11 more
2020Journal of Clinical Medicine17 citations Open access
Semantic Scholar
Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
A. Morra, M. Escala-Garcia, J. Beesley, R. Keeman +146 more
2021Breast Cancer Research16 citations Open access
Semantic Scholar
Acute myeloid leukemia‐induced functional inhibition of healthy CD34+ hematopoietic stem and progenitor cells
P. Jäger, S. Geyh, S. Twarock, Ron-Patrick Cadeddu +17 more
2021Stem Cells15 citations Open access
Semantic Scholar
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
Stefanie H. Müller, A. Lai, M. Valkovskaya, K. Michailidou +203 more
2023Genome Medicine14 citations Open access
Semantic Scholar
Circulating cell-free DNA variables as marker of ovarian cancer patients: A pilot study
S. Stamenković, Jie Cheng, H. Surowy, B. Burwinkel +1 more
2020Cancer Biomarkers13 citations Open access
Semantic Scholar
QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum
M. Föhrenbach, R. Jamra, A. Borkhardt, T. Brozou +9 more
2020Clinical Genetics12 citations Open access
Semantic Scholar
Identification and characterization of novel associations in the CASP 8 / ALS 2 CR 12 region on chromosome 2 with breast cancer risk
Weiqiang Lin, N. Camp, M. Ghoussaini, J. Beesley +132 more
201411 citations
Semantic Scholar
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype
L. Averdunk, H. Sticht, H. Surowy, H. Lüdecke +15 more
2021Journal of molecular medicine10 citations Open access
Semantic Scholar
Clinical and molecular characterization of the BRCA2 p.Asn3124Ile variant reveals substantial evidence for pathogenic significance
H. Surowy, C. Sutter, Max Mittnacht, R. Klaes +13 more
2014Breast Cancer Research and Treatment10 citations
Semantic Scholar
Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X
K. Bucksch, S. Zachariae, A. Ahadova, S. Aretz +20 more
2021International Journal of Cancer9 citations Open access
Semantic Scholar
Interference in transcription of overexpressed genes by promoter-proximal downstream sequences
A. Turchinovich, H. Surowy, A. Tonevitsky, B. Burwinkel
2016Scientific Reports9 citations Open access
Semantic Scholar
Increased Radiosensitivity as an Indicator of Genes Conferring Breast Cancer Susceptibility
D. Varga, W. Vogel, A. Bender, H. Surowy +4 more
2007Strahlentherapie und Onkologie (Print)9 citations
Semantic Scholar
Two truncating variants in FANCC and breast cancer risk
T. Dörk, P. Peterlongo, A. Mannermaa, M. Bolla +199 more
2019Scientific Reports8 citations Open access
Semantic Scholar
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
J. Baxter, N. Johnson, K. Tomczyk, Andrea Gillespie +179 more
2021American Journal of Human Genetics7 citations Open access
Semantic Scholar
Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain
L. Averdunk, K. Al-Thihli, H. Surowy, Hermann-Josef Lüdecke +13 more
2022Clinical Genetics6 citations Open access
Semantic Scholar
The prostate cancer risk locus at 10q11 is associated with DNA repair capacity.
A. Rinckleb, H. Surowy, Manuel Luedeke, D. Varga +4 more
2012DNA Repair6 citations
Semantic Scholar

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