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D. Drichel · SciRah

Researcher profile · Semantic Scholar

D. Drichel

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D. Drichel — researcher profile on SciRah

h-index: 20
Works: 52
Citations: 5,712

Most-cited papers

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Brian W. Kunkle, B. Grenier-Boley, R. Sims, J. Bis +464 more
2019Nature Genetics2,490 citations Open access
Semantic Scholar
New insights into the genetic etiology of Alzheimer’s disease and related dementias
C. Bellenguez, F. Küçükali, I. Jansen, L. Kleineidam +496 more
2022Nature Genetics1,984 citations Open access
Semantic Scholar
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology.
S. Heilmann, A. Kiefer, Nadine Fricker, D. Drichel +22 more
2013Journal of Investigative Dermatology118 citations Open access
Semantic Scholar
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits
B. Quach, Michael J. Bray, Nathan C. Gaddis, Meng-Zhen Liu +42 more
2020Nature Communications107 citations Open access
Semantic Scholar
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans
B. Krause-Kyora, Marcel Nutsua, Lisa Boehme, Federica Pierini +19 more
2018Nature Communications92 citations Open access
Semantic Scholar
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Brian W. Kunkle, B. Grenier-Boley, R. Sims, J. Bis +464 more
2019Nature Genetics85 citations Open access
Semantic Scholar
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
S. Heilmann-Heimbach, C. Herold, L. Hochfeld, A. M. Hillmer +32 more
2017Nature Communications79 citations Open access
Semantic Scholar
Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases
I. Spier, D. Drichel, M. Kerick, J. Kirfel +16 more
2015Journal of Medical Genetics67 citations Open access
Semantic Scholar
High-Throughput miRNA and mRNA Sequencing of Paired Colorectal Normal, Tumor and Metastasis Tissues and Bioinformatic Modeling of miRNA-1 Therapeutic Applications
Christina Röhr, M. Kerick, A. Fischer, Alexander Kühn +18 more
2013PLoS ONE63 citations Open access
Semantic Scholar
Syddansk Universitet Identification and characterization of two functional variants in the human longevity gene
F. Flachsbart, Janina Dose, Liljana Gentschew, C. Geismann +30 more
201756 citations
Semantic Scholar
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.
M. Thelen, C. Razquín, I. Hernández, A. Gorostidi +44 more
2014Neurobiology of Aging55 citations Open access
Semantic Scholar
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis
I. Spier, M. Kerick, D. Drichel, S. Horpaopan +16 more
2016Familial Cancer54 citations Open access
Semantic Scholar
Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
S. Redler, F. F. Brockschmidt, R. Tazi-Ahnini, D. Drichel +14 more
2012British Journal of Dermatology54 citations
Semantic Scholar
SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.
A. Ramírez, W. M. van der Flier, C. Herold, D. Ramonet +33 more
2014Human Molecular Genetics51 citations Open access
Semantic Scholar
Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing
A. Hoebel, D. Drichel, M. van de Vorst, A. Böhmer +26 more
2017Journal of dentistry research41 citations
Semantic Scholar
Identification and characterization of two functional variants in the human longevity gene FOXO3
F. Flachsbart, Janina Dose, Liljana Gentschew, C. Geismann +30 more
2017Nature Communications36 citations Open access
Semantic Scholar
Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss.
S. Redler, K. Dobson, D. Drichel, S. Heilmann +17 more
2013Journal of dermatological science (Amsterdam)32 citations
Semantic Scholar
Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
Rima Nuwaihyd, S. Redler, S. Heilmann, D. Drichel +18 more
2014Archives of Dermatological Research27 citations
Semantic Scholar
Selected variants of the steroid‐5‐alpha‐reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified
S. Redler, R. Tazi-Ahnini, D. Drichel, M. P. Birch +13 more
2012Experimental Dermatology26 citations Open access
Semantic Scholar
Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations
B. Noyvert, A. M. Erzurumluoglu, D. Drichel, S. Omland +22 more
2023medRxiv22 citations Open access
Semantic Scholar
Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
S. Redler, M. P. Birch, D. Drichel, K. Dobson +11 more
2011British Journal of Dermatology19 citations
Semantic Scholar
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease
Sophie A Riesmeijer, Zoha Kamali, M. Ng, D. Drichel +10 more
2024Nature Communications18 citations Open access
Semantic Scholar
mARC1 in MASLD: Modulation of lipid accumulation in human hepatocytes and adipocytes
Amanda K. Jones, Besnik Bajrami, Morgan K Campbell, A. Erzurumluoglu +33 more
2024Hepatology Communications14 citations Open access
Semantic Scholar
Quick, “Imputation-free” meta-analysis with proxy-SNPs
C. Meesters, M. Leber, C. Herold, Marina Angisch +4 more
2012BMC Bioinformatics14 citations Open access
Semantic Scholar
Integrated Genome-Wide Pathway Association Analysis with INTERSNP
C. Herold, M. Mattheisen, A. Lacour, T. Vaitsiakhovich +3 more
2012Human Heredity13 citations Open access
Semantic Scholar
Novel genetic matching methods for handling population stratification in genome-wide association studies
A. Lacour, Vitalia Schüller, D. Drichel, C. Herold +7 more
2015BMC Bioinformatics12 citations Open access
Semantic Scholar
Identi fi cation and characterization of two functional variants in the human longevity gene FOXO 3
Liljana Gentschew, C. Geismann, A. Caliebe, Carolin Knecht +28 more
201811 citations
Semantic Scholar
Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS)
S. Horpaopan, J. Kirfel, S. Peters, M. Kloth +14 more
2017Hereditary Cancer in Clinical Practice11 citations Open access
Semantic Scholar
Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample
A. Mobascher, A. Diaz-Lacava, Michael Wagner, J. Gallinat +14 more
2016PLoS ONE10 citations Open access
Semantic Scholar
The oestrogen receptor 2 (ESR2) gene in female‐pattern hair loss: replication of association with rs10137185 in German patients
S. Redler, P. Birch, D. Drichel, P. Hofmann +18 more
2014British Journal of Dermatology9 citations
Semantic Scholar
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair loss
H. Mahmoudi, S. Redler, P. Birch, D. Drichel +14 more
2013Archives of Dermatological Research9 citations
Semantic Scholar
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans
B. Krause-Kyora, Marcel Nutsua, Lisa Boehme, Federica Pierini +19 more
2018Nature Communications8 citations Open access
Semantic Scholar
METAINTER: meta-analysis of multiple regression models in genome-wide association studies
T. Vaitsiakhovich, D. Drichel, C. Herold, A. Lacour +1 more
2015Bioinform.8 citations Open access
Semantic Scholar
Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish models
Nina Ishorst, Selina Hölzel, Carola Greve, Öznur Yılmaz +24 more
2024European Journal of Human Genetics7 citations Open access
Semantic Scholar
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores
Nina Ishorst, L. Henschel, F. Thieme, D. Drichel +31 more
2022Molecular Genetics & Genomic Medicine5 citations Open access
Semantic Scholar
Analysis of the progression of systolic blood pressure using imputation of missing phenotype values
T. Vaitsiakhovich, D. Drichel, Marina Angisch, T. Becker +2 more
2014BMC Proceedings5 citations Open access
Semantic Scholar
The exhaustive genomic scan approach, with an application to rare-variant association analysis
George Kanoungi, M. Nothnagel, T. Becker, D. Drichel
2019European Journal of Human Genetics3 citations Open access
Semantic Scholar
Die Unsichtbaren. Menschen mit Trisomie 21 in Archäologie und Anthropologie
U. Halle, Cathrin Hähn, S. Krause, Ben Krause-Kyora +3 more
20193 citations
Semantic Scholar
Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3
F. Flachsbart, Janina Dose, Liljana Gentschew, C. Geismann +30 more
2018Nature Communications3 citations Open access
Semantic Scholar
Rare Variant Testing of Imputed Data: An Analysis Pipeline Typified
D. Drichel, C. Herold, A. Lacour, A. Ramírez +6 more
2014Human Heredity2 citations
Semantic Scholar
A One-Degree-of-Freedom Test for Supra-Multiplicativity of SNP Effects
C. Herold, A. Ramírez, D. Drichel, A. Lacour +5 more
2013PLoS ONE2 citations Open access
Semantic Scholar
Correlation Functions in N=3 Superconformal Theory
D. Drichel, M. Flohr
20102 citations
Semantic Scholar
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis
I. Spier, M. Kerick, D. Drichel, S. Horpaopan +16 more
2016Familial Cancer1 citations Open access
Semantic Scholar
P4‐087: Genetic complexity in the BIN1 locus
A. Ramírez, C. Herold, Piotr Lewczuk, A. Lacour +21 more
20121 citations Open access
Semantic Scholar
Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3
F. Flachsbart, Janina Dose, Liljana Gentschew, C. Geismann +30 more
2018Nature Communications0 citations Open access
Semantic Scholar
Author’s response to reviews Title: Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS) Authors:
S. Horpaopan, J. Kirfel, M. Kloth, J. Altmuller +5 more
20170 citations
Semantic Scholar
Contents Vol. 78, 2014
Kelly M. Burkett, B. McNeney, Jinko Graham, C. Greenwood +31 more
2015Human Heredity0 citations
Semantic Scholar
INTERSNP - Genome-wide Interaction Analysis from the University of Bonn
C. Herold, T. Becker, D. Drichel, A. Lacour +2 more
20150 citations
Semantic Scholar
Power values a of SMT under 3-SNP-recessive models.
C. Herold, A. Ramírez, D. Drichel, A. Lacour +5 more
20130 citations Open access
Semantic Scholar
Session B: Androgenetic Alopecia – Part II
A. Mareeva, Sergey Rotanov, I. Volkov, S. Redler +14 more
2011International Journal of Trichology0 citations
Semantic Scholar

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