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Author Details
Full Name
Felix Grassmann
Affiliation
Karolinska Institutet
ORCID
Career Start Year
2011
Papers
68
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36707629
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.
Eur J Hum Genet
2023
37950326
Correction: Bipolar haemostatic forceps versus standard therapy by haemoclipâ¿¿+â¿¿/â¿¿-â¿¿epinephrine injection as initial endoscopic treatment in active non-variceal upper GI bleeding: study protocol for a prospective, randomized multicentre trial (BeBop-Trial).
Trials
2023
37322511
Bipolar haemostatic forceps versus standard therapy by haemoclipâ¿¿+â¿¿/â¿¿-â¿¿epinephrine injection as initial endoscopic treatment in active non-variceal upper GI bleeding: study protocol for a prospective, randomized multicentre trial (BeBop-Trial).
Trials
2023
37444426
Spectrum and Frequency of Germline <i>FANCM</i> Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases.
Cancers (Basel)
2023
37243749
Risk of estrogen receptor-specific breast cancer by family history of estrogen receptor subtypes and other cancers.
J Natl Cancer Inst
2023
37243694
Prediction of breast cancer risk for sisters of women attending screening.
J Natl Cancer Inst
2023
36536985
Low leukocyte mitochondrial DNA abundance drives atherosclerotic cardiovascular diseases: a cohort and Mendelian randomization study.
Cardiovasc Res
2023
34605899
Seed sequence polymorphism rs2168518 and allele-specific target gene regulation of hsa-miR-4513.
Hum Mol Genet
2022
35793595
The association between mitochondrial DNA abundance and stroke: A combination of multivariable-adjusted survival and Mendelian randomization analyses.
Atherosclerosis
2022
35525297
Artificial intelligence-based strategies to identify patient populations and advance analysis in age-related macular degeneration clinical trials.
Exp Eye Res
2022
36108770
Systems genomics in age-related macular degeneration.
Exp Eye Res
2022
35867128
Assessment of the bi-directional relationship between blood mitochondrial DNA copy number and type 2 diabetes mellitus: a multivariable-adjusted regression and Mendelian randomisation study.
Diabetologia
2022
36302047
Percutaneous transhepatic or endoscopic ultrasound-guided biliary drainage in malignant distal bile duct obstruction using a self-expanding metal stent: Study protocol for a prospective European multicenter trial (PUMa trial).
PLoS One
2022
35026490
Interval breast cancer is associated with interferon immune response.
Eur J Cancer
2022
35293856
Risk of heart disease following treatment for breast cancer - results from a population-based cohort study.
Elife
2022
33385171
Deciphering the genetic and epidemiological landscape of mitochondrial DNA abundance.
Hum Genet
2021
33547498
Correction to: Deciphering the genetic and epidemiological landscape of mitochondrial DNA abundance.
Hum Genet
2021
34097750
Lymph node metastases in breast cancer: Investigating associations with tumor characteristics, molecular subtypes and polygenic risk score using a continuous growth model.
Int J Cancer
2021
34338750
Mammographic features are associated with cardiometabolic disease risk and mortality.
Eur Heart J
2021
34284099
CYP2D6 genotype predicts tamoxifen discontinuation and drug response: a secondary analysis of the KARISMA trial.
Ann Oncol
2021
31134332
Insights into the loss of the Y chromosome with age in control individuals and in patients with age-related macular degeneration using genotyping microarray data.
Hum Genet
2020
31800347
CYP2D6 Genotype Predicts Tamoxifen Discontinuation and Prognosis in Patients With Breast Cancer.
J Clin Oncol
2020
32036684
The association of single nucleotide polymorphisms (SNPs) with breast density and breast cancer survival: the Malmö Diet and Cancer Study.
Acta Radiol
2020
33110144
A systems genomics approach to uncover the molecular properties of cancer genes.
Sci Rep
2020
32838791
Hyperthyroidism is associated with breast cancer risk and mammographic and genetic risk predictors.
BMC Med
2020
32870927
A mega-analysis of expression quantitative trait loci in retinal tissue.
PLoS Genet
2020
32843070
Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease.
BMC Med Genomics
2020
32294914
A Circulating MicroRNA Profile in a Laser-Induced Mouse Model of Choroidal Neovascularization.
Int J Mol Sci
2020
31474439
Complement C3 Inhibitor Pegcetacoplan for Geographic Atrophy Secondary to Age-Related Macular Degeneration: A Randomized Phase 2 Trial.
Ophthalmology
2020
30643219
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides.
Genet Med
2019
31641120
Interval breast cancer is associated with other types of tumors.
Nat Commun
2019
30158665
Y chromosome mosaicism is associated with age-related macular degeneration.
Eur J Hum Genet
2019
29929185
Spectral Domain Optical Coherence Tomography Allows the Unification of Clinical Decision Making for the Evaluation of Choroidal Neovascularization Activity.
Ophthalmologica
2019
31212395
Cost-effective molecular inversion probe-based ABCA4 sequencing reveals deep-intronic variants in Stargardt disease.
Hum Mutat
2019
30777091
The agonistic TSPO ligand XBD173 attenuates the glial response thereby protecting inner retinal neurons in a murine model of retinal ischemia.
J Neuroinflammation
2019
31120506
Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration.
JAMA Ophthalmol
2019
30324434
Conduct and Quality Control of Differential Gene Expression Analysis Using High-Throughput Transcriptome Sequencing (RNASeq).
Methods Mol Biol
2019
29650998
A mega-analysis of expression quantitative trait loci (eQTL) provides insight into the regulatory architecture of gene expression variation in liver.
Sci Rep
2018
30071029
Evaluation of serum sphingolipids and the influence of genetic risk factors in age-related macular degeneration.
PLoS One
2018
29529059
Investigating the modulation of genetic effects on late AMD by age and sex: Lessons learned and two additional loci.
PLoS One
2018
29721950
Pleiotropic Effects of Risk Factors in Age-Related Macular Degeneration and Seemingly Unrelated Complex Diseases.
Adv Exp Med Biol
2018
29686068
Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (<i>CFH</i>) gene family.
Proc Natl Acad Sci U S A
2018
29653860
A Deep Learning Algorithm for Prediction of Age-Related Eye Disease Study Severity Scale for Age-Related Macular Degeneration from Color Fundus Photography.
Ophthalmology
2018
27658786
An Eye on Age-Related Macular Degeneration: The Role of MicroRNAs in Disease Pathology.
Mol Diagn Ther
2017
28086806
Age-related macular degeneration associated polymorphism rs10490924 in ARMS2 results in deficiency of a complement activator.
J Neuroinflammation
2017
28347358
Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.
Genome Med
2017
28118664
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Invest Ophthalmol Vis Sci
2017
27879347
Recombinant Haplotypes Narrow the ARMS2/HTRA1 Association Signal for Age-Related Macular Degeneration.
Genetics
2017
26691988
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
Nat Genet
2016
27893849
Features of Age-Related Macular Degeneration in the General Adults and Their Dependency on Age, Sex, and Smoking: Results from the German KORA Study.
PLoS One
2016
1 - 50 of 68
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Michael B Gorin
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