Ludmila Prokunina-Olsson
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Russian medical geneticist
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Why Is Ludmila Prokunina-Olsson Influential?
(Suggest an Edit or Addition)According to Wikipedia, Ludmila Prokunina-Olsson is a molecular medical geneticist who conducts genetic and functional analyses downstream of genome-wide association studies for various human traits, including cancer, immune and infectious diseases. She is chief of the Laboratory of Translational Genomics at the National Cancer Institute.
Ludmila Prokunina-Olsson's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants (2007) (2840)
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus (2010) (1048)
- A variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virus (2013) (874)
- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) (2009) (578)
- Detectable clonal mosaicism and its relationship to aging and cancer (2012) (512)
- A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci (2010) (423)
- Interferons and viruses induce a novel truncated ACE2 isoform and not the full-length SARS-CoV-2 receptor (2020) (189)
- Endogenous intrahepatic IFNs and association with IFN-free HCV treatment outcome. (2014) (185)
- COVID-19 and emerging viral infections: The case for interferon lambda (2020) (159)
- A new haplotype of PDCD1 is associated with rheumatoid arthritis in Hong Kong Chinese. (2005) (159)
- A Functional Variant at a Prostate Cancer Predisposition Locus at 8q24 Is Associated with PVT1 Expression (2011) (159)
- A variant upstream of IFNL 3 ( IL 28 B ) creating a novel interferon gene IFNL 4 is associated with impaired clearance of hepatitis C virus (2012) (152)
- Genome-wide association study identifies multiple loci associated with bladder cancer risk. (2014) (136)
- IL‐29 is the dominant type III interferon produced by hepatocytes during acute hepatitis C virus infection (2012) (133)
- Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors (2016) (133)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. (2015) (133)
- IFN-λ4: the paradoxical new member of the interferon lambda family. (2014) (129)
- Tissue-specific alternative splicing of TCF7L2 (2009) (110)
- Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer. (2013) (104)
- A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene (2009) (101)
- Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort (2007) (100)
- A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3. (2011) (97)
- Selection on a Variant Associated with Improved Viral Clearance Drives Local, Adaptive Pseudogenization of Interferon Lambda 4 (IFNL4) (2014) (93)
- Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver (2011) (92)
- Characterization of large structural genetic mosaicism in human autosomes. (2015) (91)
- IFNL4-ΔG genotype is associated with slower viral clearance in hepatitis C, genotype-1 patients treated with sofosbuvir and ribavirin. (2014) (86)
- Common genetic variants in the PSCA gene influence gene expression and bladder cancer risk (2012) (81)
- Association of the IFNL4-ΔG Allele With Impaired Spontaneous Clearance of Hepatitis C Virus. (2014) (78)
- Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (2016) (72)
- APOBEC Mutagenesis and Copy-Number Alterations Are Drivers of Proteogenomic Tumor Evolution and Heterogeneity in Metastatic Thoracic Tumors (2019) (71)
- Comparison of functional variants in IFNL4 and IFNL3 for association with HCV clearance. (2015) (69)
- Weak Induction of Interferon Expression by SARS-CoV-2 Supports Clinical Trials of Interferon Lambda to Treat Early COVID-19. (2020) (68)
- Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer. (2012) (68)
- Genome-wide methylation profiling identifies novel methylated genes in neuroblastoma tumors (2016) (65)
- Genome-wide association meta-analysis of functional outcome after ischemic stroke (2019) (64)
- Expression of the selenoprotein S (SELS) gene in subcutaneous adipose tissue and SELS genotype are associated with metabolic risk factors (2011) (61)
- A Common Missense Variant in the ATP Receptor P2X7 Is Associated with Reduced Risk of Cardiovascular Events (2012) (58)
- IFN-λ4 Attenuates Antiviral Responses by Enhancing Negative Regulation of IFN Signaling (2017) (55)
- Endogenous Acute Phase Serum Amyloid A Lacks Pro-Inflammatory Activity, Contrasting the Two Recombinant Variants That Activate Human Neutrophils through Different Receptors (2013) (53)
- Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness (2015) (53)
- Weak Induction of Interferon Expression by Severe Acute Respiratory Syndrome Coronavirus 2 Supports Clinical Trials of Interferon-λ to Treat Early Coronavirus Disease 2019 (2020) (50)
- Tenomodulin is highly expressed in adipose tissue, increased in obesity, and down-regulated during diet-induced weight loss. (2009) (48)
- NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations (2010) (47)
- Genome-wide interaction study of smoking and bladder cancer risk. (2014) (46)
- Evaluation of a variant in the transcription factor 7‐like 2 (TCF7L2) gene and prostate cancer risk in a population‐based study (2008) (44)
- Genetic Variation Within the Interleukin-1 Gene Cluster and Ischemic Stroke (2012) (44)
- Alternative Splicing of TCF7L2 Gene in Omental and Subcutaneous Adipose Tissue and Risk of Type 2 Diabetes (2009) (43)
- Large-Scale Pathway-Based Analysis of Bladder Cancer Genome-Wide Association Data from Five Studies of European Background (2012) (42)
- Splicing Diversity of the Human OCLN Gene and Its Biological Significance for Hepatitis C Virus Entry (2010) (41)
- Immune gene expression profiling reveals heterogeneity in luminal breast tumors (2019) (40)
- Common Genetic Variants in miR-1206 (8q24.2) and miR-612 (11q13.3) Affect Biogenesis of Mature miRNA Forms (2012) (40)
- Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK. (2010) (40)
- Genetics of the Human Interferon Lambda Region (2019) (35)
- Genetic variation on chromosome 9p21 shows association with the ischaemic stroke subtype large‐vessel disease in a Swedish sample aged ≤70 (2011) (35)
- Modification of Occupational Exposures on Bladder Cancer Risk by Common Genetic Polymorphisms. (2015) (34)
- Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population. (2015) (34)
- Expression of Interferon Lambda 4 Is Associated with Reduced Proliferation and Increased Cell Death in Human Hepatic Cells (2015) (33)
- Genetic Variation at the BDNF Locus: Evidence for Association with Long-Term Outcome after Ischemic Stroke (2014) (33)
- Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry. (2016) (33)
- Plasma C3 and C3a Levels in Cryptogenic and Large-Vessel Disease Stroke: Associations with Outcome (2011) (32)
- Association between genetic variation on chromosome 9p21 and aneurysmal subarachnoid haemorrhage (2010) (31)
- Evaluating the Causal Link Between Malaria Infection and Endemic Burkitt Lymphoma in Northern Uganda: A Mendelian Randomization Study (2017) (31)
- The TGR5 gene is expressed in human subcutaneous adipose tissue and is associated with obesity, weight loss and resting metabolic rate (2013) (31)
- A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study (2014) (29)
- Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes (2018) (29)
- Genetic Variant on Chromosome 12p13 Does Not Show Association to Ischemic Stroke in 3 Swedish Case-Control Studies (2011) (28)
- Association of serum amyloid A levels with adipocyte size and serum levels of adipokines: differences between men and women. (2009) (28)
- APOBEC-mediated Mutagenesis as a Likely Cause of FGFR3 S249C Mutation Over-representation in Bladder Cancer. (2019) (28)
- No effect of cancer-associated SNP rs6983267 in the 8q24 region on co-expression of MYC and TCF7L2 in normal colon tissue (2009) (27)
- IL28B rs12979860 genotype and spontaneous clearance of hepatitis C virus in a multi-ethnic cohort of injection drug users: evidence for a supra-additive association. (2011) (27)
- Differential urinary specific gravity as a molecular phenotype of the bladder cancer genetic association in the urea transporter gene, SLC14A1 (2013) (26)
- Detection of bladder, breast and prostate cancer using serum and tissue miRNA profiling (2011) (26)
- IFNL4-ΔG Allele Is Associated with an Interferon Signature in Tumors and Survival of African-American Men with Prostate Cancer (2018) (25)
- Genetic Variant as a Selection Marker for Anti–Prostate Stem Cell Antigen Immunotherapy of Bladder Cancer (2012) (25)
- IFNL4-ΔG is associated with prostate cancer among men at increased risk of sexually transmitted infections (2018) (25)
- Expression analysis of loci associated with type 2 diabetes in human tissues (2010) (25)
- Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types (2015) (24)
- Refining the Prostate Cancer Genetic Association within the JAZF1 Gene on Chromosome 7p15.2 (2010) (24)
- Genetic variants of GSK3B are associated with biomarkers for Alzheimer's disease and cognitive function. (2015) (24)
- Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke? (2013) (23)
- Comparative drug pair screening across multiple glioblastoma cell lines reveals novel drug-drug interactions. (2013) (23)
- Cardioembolic and Small Vessel Disease Stroke Show Differences in Associations between Systemic C3 Levels and Outcome (2013) (23)
- Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 (2020) (22)
- Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression (2013) (21)
- The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease. (2014) (21)
- Evidence for neuroendocrine function of a unique splicing form of TCF7L2 in human brain, islets and gut (2009) (20)
- Genetic variation in complement component C3 shows association with ischaemic stroke (2011) (19)
- CDKN2B expression and subcutaneous adipose tissue expandability: Possible influence of the 9p21 atherosclerosis locus (2014) (19)
- Genetic signatures of gene flow and malaria-driven natural selection in sub-Saharan populations of the "endemic Burkitt Lymphoma belt" (2019) (19)
- A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene (2012) (19)
- The IFN-λ4 Conundrum: When a Good Interferon Goes Bad. (2019) (18)
- No association between a candidate TCF7L2 variant and risk of breast or ovarian cancer (2009) (18)
- Genetic variation at the IGF1 locus shows association with post-stroke outcome and to circulating IGF1. (2013) (18)
- In the absence of HCV infection, interferon stimulated gene expression in liver is not associated with IL28B genotype. (2010) (18)
- Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries (2022) (17)
- Exome array analysis of ischaemic stroke: results from a southern Swedish study (2016) (17)
- No Evidence for a Role of Adipose Tissue-Derived Serum Amyloid A in the Development of Insulin Resistance or Obesity-Related Inflammation in hSAA1+/− Transgenic Mice (2013) (17)
- Tissue-specific alternative splicing of TCF 7 L 2 (2009) (17)
- Comparative Functional Analysis of 12 Mammalian IFN-λ4 Orthologs (2016) (16)
- Genetic variation in the receptor for advanced glycation end‐products (RAGE) gene and ischaemic stroke (2013) (15)
- Establishment of a Transgenic Mouse Model Specifically Expressing Human Serum Amyloid A in Adipose Tissue (2011) (15)
- A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC 14 A 1 , a urea transporter gene on chromosome 18 q 12 . 3 (2011) (15)
- Associations between IgG reactivity to Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) antigens and Burkitt lymphoma in Ghana and Uganda case-control studies (2018) (14)
- Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus (2016) (14)
- Decreased risk for myocardial infarction and lower tumor necrosis factor-alpha levels in carriers of variants of the PDCD1 gene. (2006) (13)
- The Association between the Comprehensive Epstein–Barr Virus Serologic Profile and Endemic Burkitt Lymphoma (2019) (12)
- Association of the IFNL 4-Δ G Allele With Impaired Spontaneous Clearance of Hepatitis C Virus (2014) (10)
- Genomeâwide analysis of genetic determinants of circulating factorÂVIIâactivating protease (FSAP) activity (2018) (10)
- Association of Hepatitis C Virus Infection With CD4/CD8 Ratio in HIV-Positive Women (2016) (10)
- Prostate stem cell antigen (PSCA) and risk of bladder cancer: linking genotypes to functional mechanisms (2011) (9)
- Vitamin D Status and Virologic Response to HCV Therapy in the HALT-C and VIRAHEP-C Trials (2016) (9)
- Lack of association between genetic variations in the KALRN region and ischemic stroke. (2011) (9)
- APOBEC3B expression in breast cancer cell lines and tumors depends on the estrogen receptor status. (2020) (8)
- Association between variation in ADAMTS13 and aneurysmal subarachnoid hemorrhage. (2013) (8)
- NOTCH 2 in breast cancer : association of SNP rs 11249433 with gene expression in ER-positive breast tumors without TP 53 mutations (2010) (8)
- Adipose Tissue-Derived Human Serum Amyloid A Does Not Affect Atherosclerotic Lesion Area in hSAA1+/−/ApoE−/− Mice (2014) (8)
- A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor (2018) (7)
- Interferon Lambda 4 Genotype Is Not Associated with Recurrence of Oral or Genital Herpes (2015) (7)
- Intracellular Accumulation of IFN-λ4 Induces ER Stress and Results in Anti-Cirrhotic but Pro-HCV Effects (2021) (6)
- Association of donor IFNL4 genotype and non-relapse mortality after unrelated donor myeloablative haematopoietic stem-cell transplantation for acute leukaemia: a retrospective cohort study. (2020) (6)
- Metabolic Changes in Chronic Hepatitis C Patients who Carry IFNL4-ΔG and Achieve Sustained Virologic Response with Direct-Acting Antiviral Therapy. (2019) (6)
- IFN-λ4 is associated with increased risk and earlier occurrence of several common infections in African children (2021) (6)
- Association of IFNL3 and IFNL4 polymorphisms with liver‐related mortality in a multiracial cohort of HIV/HCV‐coinfected women (2015) (6)
- Impact of IFNL4-∆G genotype on sustained virologic response in hepatitis C genotype 1 patients treated with direct-acting antivirals. (2018) (5)
- No evidence for an association between genetic variation at the MMP2 and MMP9 loci and aneurysmal subarachnoid haemorrhage (2011) (5)
- When the Smoke Clears m6A from a Y Chromosome–Linked lncRNA, Men Get an Increased Risk of Cancer (2020) (5)
- Meeting Overview: Interferon Lambda-Disease Impact and Therapeutic Potential. (2019) (5)
- Targeting natural splicing plasticity of APOBEC3B restricts its expression and mutagenic activity (2021) (5)
- CDKN 2 B expression and subcutaneous adipose tissue expandability : Possible influence of the 9 p 21 atherosclerosis locus (2014) (4)
- Targeted Deep Sequencing of Bladder Tumors Reveals Novel Associations between Cancer Gene Mutations and Mutational Signatures with Major Risk Factors (2019) (4)
- Prostate stem cell antigen (PSCA) and risk of bladder cancer: linking genotypes to functional mechanisms (2011) (4)
- Factor VII antigen levels are differentially associated to etiological subtypes of ischaemic stroke (2013) (4)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (2012) (4)
- 41 NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumours without TP53 mutations (2010) (3)
- Relationship of Genotype for HLA B*57 and IFNL4 With Disease Progression in Female HIV Controllers. (2017) (3)
- Variation in the Human Leukocyte Antigen system and risk for endemic Burkitt lymphoma in northern Uganda (2020) (3)
- Statistical tests for detecting associations with groups of genetic variants: generalization, evaluation, and implementation (2012) (3)
- Changes in serum hepatitis B surface and e antigen, interferon‐inducible protein 10, and aminotransferase levels during combination therapy of immune‐tolerant chronic hepatitis B (2022) (3)
- Comparison of somatic mutation landscapes in Chinese versus European breast cancer patients (2021) (3)
- IFN-λ4 is associated with increased risk and earlier occurrence of gastrointestinal, respiratory and malarial infections in Malian children (2020) (2)
- Correction: Selection on a Variant Associated with Improved Viral Clearance Drives Local, Adaptive Pseudogenization of Interferon Lambda 4 (IFNL4) (2014) (2)
- 182 : Identification and characterization of interferon-λ4 (IFN-λ4), a novel class-2 cytokine which impairs clearance of hepatitis C virus (2013) (2)
- No evidence for an association between genetic variation at the SERPINI1 locus and ischemic stroke (2011) (2)
- TFPI gene variation and ischemic stroke. (2012) (2)
- Functional exploration of CCNE1 splicing forms as a possible link to bladder cancer susceptibility (2011) (2)
- Genetic variation at the IGF 1 locus shows association with post-stroke outcome and to circulating IGF 1 (2013) (2)
- IFNL4 - D G Allele Is Associated with an Interferon Signature in Tumors and Survival of African-American Men with Prostate Cancer (2018) (2)
- Abstract B051: IFNL4-deltaG allele is associated with an interferon signature in tumors and survival of African-American men with prostate cancer (2020) (2)
- IFN-λ4 increases the risk of gastrointestinal infections and malaria in Malian children (2020) (2)
- Common Mechanisms of Virus-Mediated Oncogenesis in Bladder Cancers Arising In Solid Organ Transplant Recipients (2021) (1)
- Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2020) (1)
- Tumor transcriptome analysis and immune infiltrate profiling suggests a role for the IFNL3/IFNL4 genomic locus in liver cancer (2018) (1)
- It Takes Two (Genomes) to Cancer: Paired Viral and Host Transcriptome Analysis Provides New Insights about EBV Carcinogenicity. (2019) (1)
- What makes the hepatitis C virus evolve? (2019) (1)
- Tenomodulin, serum amyloid A and the serum amyloid A receptor selenoprotein S - implications for metabolic disease (2010) (1)
- Abstract 4742: NOTCH2 in breast cancer: Association of SNP rs11249433 with gene expression in ER-positive breast tumors without p53 gene mutations (2010) (1)
- Title A variant upstream of IFNL 3 ( IL 28 B ) creating a novel interferon gene IFNL 4 is associated with impaired clearance of hepatitis C virus (2013) (1)
- Cancer Sequencing Gets a Little More Personal (2010) (1)
- Disinfection By-Products in Drinking Water and Bladder Cancer: Evaluation of Risk Modification by Common Genetic Polymorphisms in Two Case–Control Studies (2022) (1)
- Association between genetic variation on chromosome 9 and aneurismal subarachnoid haemorrhage (2009) (1)
- Identification of functional genetic variants associated with prostate cancer through analysis of genome-wide genetic and epigenetic datasets (2011) (1)
- Isoform-specific characterization implicates alternative splicing in APOBEC3B as a mechanism restricting APOBEC-mediated mutagenesis (2020) (1)
- A novel functional variant in 8q24 is associated with regulation of prostate stem cell antigen (PSCA) gene expression and bladder cancer risk (2011) (1)
- Abstract 2562: Bladder cancer GWAS signal at 4p16.3 affects response of TMEM129 to chemically-induced endoplasmic reticulum stress (2016) (1)
- Functional exploration of CCNE1 splicing forms as a possible link to bladder cancer susceptibility (2011) (1)
- P1306 COMPARISON OF IFNL4- ΔG AND IFNL3 3′UTR rs4803217 GENOTYPES FOR ASSOCIATION WITH HCV TREATMENT RESPONSE (2014) (1)
- Donor IFNL4 Genotype Is Associated with Transplant-Related Mortality after Unrelated Donor Myeloablative Hematopoietic Cell Transplantation in Patients with Acute Leukemia (2018) (1)
- Abstract B51: An interferon λ 4 genotype is linked to a gene expression signature in prostate tumors of African American men (2016) (0)
- O-276 Diesel exhaust exposure and somatic mutations in bladder tumors (2021) (0)
- An unusual suspect: an uncommon human-specific synonymous coding variant within the UGT1A6 gene explains a GWAS signal and protects against bladder cancer (2011) (0)
- Abstract 826: Large-scale genome-wide association study identifies multiple novel germline susceptibility variants associated with bladder cancer risk (2021) (0)
- Abstract LB-350: Tissue and serum miRNA profiling for detection of bladder, breast and prostate cancer (2011) (0)
- An interferon-stimulated transcriptionally independent isoform of ACE2 inhibits SARS-CoV-2 infection (2021) (0)
- Abstract 861: Diesel engine exhaust is associated withTP53mutations and high-risk non-muscle invasive bladder cancer (2021) (0)
- Abstract 3816: Genetic variants within JAZF1 are associated with differential binding of androgen receptor, altered mRNA expression and risk of prostate cancer (2011) (0)
- Abstract 2783: A novel functional variant is associated with regulation of the prostate stem cell antigen (PSCA) gene and bladder cancer risk in males (2011) (0)
- Abstract 2563: Analysis of a novel gene in relation to bladder cancer GWAS signals within the 20p12.2 region (2016) (0)
- Function and Aggressive Disease The 19 q 12 Bladder Cancer GWAS Signal : Association with Cyclin E Updated (2014) (0)
- Abstract 1292: Germline genetic, molecular and environmental factors modulate APOBEC mutagenesis in human tumors (2017) (0)
- Nitrated polycyclic aromatic hydrocarbon (nitro-PAH) signatures and somatic mutations in diesel exhaust-exposed bladder tumors. (2023) (0)
- Evidence for virus-mediated oncogenesis in bladder cancers arising in solid organ transplant recipients. (2023) (0)
- Abstract 4974: Allele-specific mRNA and protein expression on genetic variants of CCNE1 associated with risk of bladder cancer (2011) (0)
- Integrated proteogenomic analysis of metastatic thoracic tumors identifies APOBEC mutagenesis and copy number alterations as drivers of proteogenomic tumor evolution and heterogeneity (2018) (0)
- Detection of bladder, breast and prostate cancer using serum and tissue miRNA profiling (2011) (0)
- Abstract 1658: Post-GWAS genetic and functional studies for bladder cancer: An uncommon protective synonymous coding variant within the UGT1A6 gene explains the GWAS signal and affects cellular detoxification (2012) (0)
- Pklr Variants Associated with Acute Pain in Sickle Cell Disease Influence ATP Concentrations in Red Blood Cells (2022) (0)
- Targeting natural splicing plasticity of APOBEC3B restricts its expression and mutagenic activity (2021) (0)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (2011) (0)
- 730 HUMAN GENETIC VARIANTS LINKED TO CHRONIC HEPATITIS B ARE ASSOCIATED WITH EXPRESSION OF HLA-DPA1 AND HLA-DPB1 (2010) (0)
- Identification of functional genetic variants associated with prostate cancer through analysis of genome-wide genetic and epigenetic datasets (2011) (0)
- Abstract TP163: Exome Array Analysis of Ischemic Stroke in a South Swedish Population (2016) (0)
- Abstract LB-051: Integrative, targeted deep sequencing of bladder tumors reveals novel associations between cancer gene mutations and mutational signatures with major risk factors (2019) (0)
- Reviewers list for European Stroke Journal 2016 (2017) (0)
- Abstract 4419: Exploration of alternative pathways mediated by IFNL4 and related to cell proliferation and death in a hepatoma cell line (2016) (0)
- 1428 INVERSE CHANGES IN HEPATIC EXPRESSION OF INTERFERON LAMBDA AND ALPHA AND IFNL4 GENOTYPE ARE ASSOCIATED WITH TREATMENT RESPONSE IN SOFOSBUVIR/RIBAVIRIN TREATED HCV GENOTYPE-1 SUBJECTS (2013) (0)
- University of Southern Denmark Genome-wide analysis of genetic determinants of circulating factor VII-activating protease (FSAP) activity Olsson, (2018) (0)
- 140: Intracellular interferon lambda 4 (IFN-λ4) induces apoptotic cell death in human hepatic cells (2014) (0)
- IFN-λ4 may contribute to HCV persistence by increasing ER stress and enhancing IRF1 signaling (2020) (0)
- Intracellular expression of IFN-λ4 leads to ER stress, enhanced IRF1 signaling and decreased proliferation in hepatic cells that might protect HCV+ patients from liver cirrhosis (2020) (0)
- Erratum to: Expression analysis of loci associated with type 2 diabetes in human tissues (2010) (0)
- ABC results and inferred parameter estimates for the SDN model. (2014) (0)
- Abstract 598: APOBEC mutagenesis: a link between innate immunity and cancer (2017) (0)
- The unfolded protein response contributes to antiproliferative and proapoptotic effects of IFN-λ4 in human hepatic cells (2019) (0)
- IFNL4-ΔG is associated with prostate cancer among men at increased risk of sexually transmitted infections (2018) (0)
- IFN-λ4 induces a faster but more transient antiviral response compared to other type III interferons (2017) (0)
- Abstract 2128: Whole transcriptome sequencing in normal and cancer prostate tissue (2010) (0)
- Abstract 4617: An alternatively spliced isoform ofTMEM129shows association with bladder cancer GWAS marker rs798766 (2015) (0)
- 755 From Genome-wide Association Studies to Translational Genomics of Bladder Cancer (2012) (0)
- HBB rs334, ABO R s8176703 and Plasmodium Falciparum Positivity at Enrollment Are Independently Associated with Lower Risk for Endemic Burkitt Lymphoma in Uganda, Tanzania, Kenya, and Malawi (2022) (0)
- AMBULANCE NURSES’ PREDICTION OF ACUTE COMPUTED TOMOGRAPHY IN PATIENTS WITH STROKE/TIA-SYMPTOMS AND/OR ALTERED LEVEL OF CONSCIOUSNESS (2009) (0)
- Abstract 5126: Allele-specific effect of rs2294008 on mRNA and protein expression of the prostate stem cell antigen (PSCA) in human normal and tumor bladder tissue (2012) (0)
- Abstract A182: Apobec-mutagenesis drives mutational heterogeneity while copy number alterations drive transcriptomic and proteogenomic heterogeneity in metastatic lung adenocarcinoma and thymic carcinoma (2018) (0)
- Abstract # 10083: From Genotype to Phenotype at a Novel Cholesterol and Myocardial Infarction Locus (2010) (0)
- Abstract 944: Translational implications of the 19q12 bladder cancer GWAS signal for aggressive bladder cancer (2014) (0)
- 151: Interferon lambda 4 (IFN-λ4) induces a pro-inflammatory state in human hepatic cells which can be blocked by a monoclonal antibody (2014) (0)
- Abstract 3751: Expression analysis of the IL28A, IL28B, IL29 and IL28L genes in primary human peripheral blood mononuclear cells and hepatocytes: Effects of activation mode, time-course and genotypes (2011) (0)
- Immune gene expression profiling reveals heterogeneity in luminal breast tumors (2019) (0)
- A Conversation with Dr. Ludmila Prokunina-Olsson. (2022) (0)
- No Association of IFNL4 Genotype With Opportunistic Infections and Cancers Among Men With Human Immunodeficiency Virus 1 Infection. (2022) (0)
- Human Leukocyte Antigen Contributes to Childhood Endemic Burkitt Lymphoma in Eastern Africa: A Case-Control Association Study (2022) (0)
- Whole transcriptome sequencing of normal and tumor bladder tissue samples (2011) (0)
- Host-Pathogen Interactions: What makes the hepatitis C virus evolve? (2019) (0)
- Abstract 4680: Exploring the relationships between genetic variants within the UGT1A locus, cellular detoxification and risk of bladder cancer (2011) (0)
- Whole transcriptome sequencing of normal and tumor bladder tissue samples (2011) (0)
- 2 A FRAME-SHIFT VARIANT IN THE NOVEL IFNL4 GENE IS ASSOCIATED WITH IMPAIRED HCV CLEARANCE (2013) (0)
- A novel functional variant in 8q24 is associated with regulation of prostate stem cell antigen (PSCA) gene expression and bladder cancer risk (2011) (0)
- An unusual suspect: an uncommon human-specific synonymous coding variant within the UGT1A6 gene explains a GWAS signal and protects against bladder cancer (2011) (0)
- No evidence for an association between genetic variation at the MMP 2 and MMP 9 loci and aneurysmal subarachnoid haemorrhage (2012) (0)
- INTERFERON LAMBDA MEETING Meeting Overview: Interferon Lambda—Disease Impact and Therapeutic Potential (2019) (0)
- Call for Special Issue Papers: Interferon-Lambda (Type-3 Interferon). (2022) (0)
- ID: 89: Comparison of IFNL4-ΔG/TT and IFNL3 rs4803217 for association with hepatitis C virus clearance (2015) (0)
- Analysis of Common Infections in Malian Children Under Five: IFNL4-dG Allele Is Associated with Higher Risk and Earlier Episodes of Gastrointestinal Infections (2020) (0)
- ID: 87: Anti-proliferative and cell death-inducing effects of interferon lambda-4 (IFNL4) may contribute differentially to HCV pathogenesis and cancer (2015) (0)
- Abstract LB-337: Synergistic effects of twelve common genetic polymorphisms and smoking habits on absolute risk of bladder cancer (2012) (0)
- Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility (2021) (0)
- Genetics Helps to Find Synergy for Immune Checkpoint and Targeted Combination Therapies. (2019) (0)
- IFN-λ4 is associated with increased risk and earlier occurrence of several common infections in African children (2021) (0)
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