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Number of items: 97.


Ounpuu, Lyudmila, Klepinin, Aleksandr, Pook, Martin, Teino, Indrek, Peet, Nadezda, Paju, Kalju, Tepp, Kersti, Chekulayev, Vladimir, Shevchuk, Igor, Koks, Sulev ORCID: 0000-0001-6087-6643
et al (show 2 more authors) (2017) 2102Ep embryonal carcinoma cells have compromised respiration and shifted bioenergetic profile distinct from H9 human embryonic stem cells. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1861 (8). pp. 2146-2154.


Koks, Sulev ORCID: 0000-0001-6087-6643 and Koks, Gea
(2017) Activation of GPR15 and its involvement in the biological effects of smoking. EXPERIMENTAL BIOLOGY AND MEDICINE, 242 (11). pp. 1207-1212.


Asser, Andres, Koks, Sulev ORCID: 0000-0001-6087-6643, Soomets, Ursel, Terasmaa, Anton, Sauk, Martin, Eltermaa, Mall, Piip, Piret, Ubhayasekera, Kumari, Bergquist, Jonas and Taba, Pille
(2019) Acute effects of methcathinone and manganese in mice: A dose response study. HELIYON, 5 (9). e02475-.


Laius, Ott, Pisarev, Heti, Maasalu, Katre, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2017) Adherence to osteoporosis medicines in Estonia-a comprehensive 15-year retrospective prescriptions database study. ARCHIVES OF OSTEOPOROSIS, 12 (1). 59-.


Rothzerg, Emel, Ho, Xuan D, Xu, Jiake, Wood, David, Martson, Aare, Maasalu, Katre and Koks, Sulev ORCID: 0000-0001-6087-6643
(2020) Alternative splicing of leptin receptor overlapping transcript in osteosarcoma. EXPERIMENTAL BIOLOGY AND MEDICINE, 245 (16). pp. 1437-1443.


Ho, Xuan D, Nguyen, Hoang G, Trinh, Le H, Reimann, Ene, Prans, Ele, Koks, Gea, Maasalu, Katre, Le, Van Q, Nguyen, Van H, Le, Nghi TN
et al (show 4 more authors) (2017) Analysis of the Expression of Repetitive DNA Elements in Osteosarcoma. FRONTIERS IN GENETICS, 8 (NOV). 193-.


Vetkas, Artur, Prans, Ele, Koks, Sulev ORCID: 0000-0001-6087-6643, Ratsep, Tonu and Asset, Toomas
(2020) Aneurysmal subarachnoid haemorrhage: Effect of CRHR1 genotype on mental health-related quality of life. SCIENTIFIC REPORTS, 10 (1). 724-.


Vetkas, Artur, Prans, Ele, Koks, Sulev ORCID: 0000-0001-6087-6643, Ratsep, Tonu and Asser, Toomas
(2020) Aneurysmal subarachnoid haemorrhage: effect of CRHR1 genotype on fatigue and depression. BMC NEUROLOGY, 20 (1). 142-.


Maegi, Agnes, Unt, Eve, Prans, Ele, Raus, Liina, Eha, Jaan, Veraksits, Alar, Kingo, Kuelli and Koks, Sulev ORCID: 0000-0001-6087-6643
(2016) The Association Analysis between ACE and ACTN3 Genes Polymorphisms and Endurance Capacity in Young Cross-Country Skiers: Longitudinal Study. JOURNAL OF SPORTS SCIENCE AND MEDICINE, 15 (2). pp. 287-294.


Traks, Tanel, Karelson, Maire, Reimann, Ene, Ratsep, Ranno, Silm, Helgi, Vasar, Eero, Koks, Sulev ORCID: 0000-0001-6087-6643 and Kingo, Kulli
(2016) Association analysis of class II cytokine and receptor genes in vitiligo patients. HUMAN IMMUNOLOGY, 77 (5). pp. 375-381.


Benzian-Olsson, Natashia, Dand, Nick, Chaloner, Charlotte, Bata-Csorgo, Zsuzsa, Borroni, Riccardo, Burden, A David, Cooper, Hywel L, Cornelius, Victoria, Cro, Suzie, Dasandi, Tejus
et al (show 22 more authors) (2020) Association of Clinical and Demographic Factors With the Severity of Palmoplantar Pustulosis. JAMA Dermatol, 156 (11). pp. 1216-1222.


Koks, Gea, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2021) At the dawn of the transcriptomic medicine. EXPERIMENTAL BIOLOGY AND MEDICINE, 246 (3). pp. 286-292.


Koks, Sulev ORCID: 0000-0001-6087-6643, Williams, Robert W, Quinn, John ORCID: 0000-0003-3551-7803, Farzaneh, Farzin, Conran, Nicola, Tsai, Shaw-Jeng, Awandare, Gordon and Goodman, Steven R
(2020) COVID-19: Time for precision epidemiology. EXPERIMENTAL BIOLOGY AND MEDICINE, 245 (8). pp. 677-679.


Fröhlich, Alexander, Hughes, Lauren S, Middlehurst, Ben ORCID: 0000-0002-2603-2719, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Koks, Sulev ORCID: 0000-0001-6087-6643 and Quinn, John P ORCID: 0000-0003-3551-7803
(2023) CRISPR deletion of a SINE-VNTR-<i>Alu</i> (SVA_67) retrotransposon demonstrates its ability to differentially modulate gene expression at the <i>MAPT</i> locus. Frontiers in neurology, 14. 1273036-.


Lantto, Tiina A, Laakso, Into, Dorman, HJ Damien, Mauriala, Timo, Hiltunen, Raimo, Koks, Sulev ORCID: 0000-0001-6087-6643 and Raasmaja, Atso
(2016) Cellular Stress and p53-Associated Apoptosis by <i>Juniperus communis</i> L. Berry Extract Treatment in the Human SH-SY5Y Neuroblastoma Cells. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 17 (7). E1113-.


Savage, Abigail L, Iacoangeli, Alfredo, Schumann, Gerald G, Rubio-Roldan, Alejandro, Garcia-Perez, Jose L, Al Khleifat, Ahmad, Koks, Sulev ORCID: 0000-0001-6087-6643, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Al-Chalabi, Ammar and Quinn, John P ORCID: 0000-0003-3551-7803
(2022) Characterisation of retrotransposon insertion polymorphisms in whole genome sequencing data from individuals with amyotrophic lateral sclerosis. GENE, 843. 146799-.


Frohlich, Alexander, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Koks, Sulev ORCID: 0000-0001-6087-6643 and Quinn, John P ORCID: 0000-0003-3551-7803
(2022) Characterisation of the Function of a SINE-VNTR-<i>Alu</i> Retrotransposon to Modulate Isoform Expression at the <i>MAPT</i> Locus. FRONTIERS IN MOLECULAR NEUROSCIENCE, 15. 815695-.


Hade, Andreas-Christian, Philips, Mari-Anne, Reimann, Ene, Jagomae, Toomas, Eskla, Kattri-Liis, Traks, Tanel, Prans, Ele, Koks, Sulev ORCID: 0000-0001-6087-6643, Vasar, Eero and Vali, Marika
(2021) Chronic Alcohol Use Induces Molecular Genetic Changes in the Dorsomedial Thalamus of People with Alcohol-Related Disorders. BRAIN SCIENCES, 11 (4). 435-.


Twelves, Sophie, Mostafa, Alshimaa, Dand, Nick, Burri, Elias, Farkas, Katalin, Wilson, Rosemary, Cooper, Hywel L, Irvine, Alan D, Oon, Hazel H, Kingo, Kulli
et al (show 21 more authors) (2019) Clinical and genetic differences between pustular psoriasis subtypes. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 143 (3). pp. 1021-1026.


Nomm, Monika, Ivask, Marilin, Paern, Pille, Reimann, Ene, Koks, Sulev ORCID: 0000-0001-6087-6643 and Jaakma, Ulle
(2024) Detecting Embryo Developmental Potential by Single Blastomere RNA-Seq. GENES, 14 (3). 569-.


Pytte, Julia, Flynn, Loren L, Anderton, Ryan S, Mastaglia, Frank L, Theunissen, Frances, James, Ian, Pfaff, Abigail, Koks, Sulev ORCID: 0000-0001-6087-6643, Saunders, Ann M, Bedlack, Richard
et al (show 6 more authors) (2020) Disease-modifying effects of an <i>SCAF4</i> structural variant in a predominantly <i>SOD1</i> ALS cohort. NEUROLOGY-GENETICS, 6 (4). e470-.


Blunder, Stefan, Koks, Sulev ORCID: 0000-0001-6087-6643, Koks, Gea, Reimann, Ene, Hackl, Hubert, Gruber, Robert, Moosbrugger-Martinz, Verena, Schmuth, Matthias and Dubrac, Sandrine
(2018) Enhanced Expression of Genes Related to Xenobiotic Metabolism in the Skin of Patients with Atopic Dermatitis but Not with Ichthyosis Vulgaris. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 138 (1). pp. 98-108.


Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004 and Quinn, John P ORCID: 0000-0003-3551-7803
(2021) Expression Quantitative Trait Loci (eQTLs) Associated with Retrotransposons Demonstrate their Modulatory Effect on the Transcriptome. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 22 (12). 6319-.


Savage, Abigail L ORCID: 0000-0002-2231-9800, Lopez, Ana Illera, Iacoangeli, Alfredo, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Smith, Bradley, Troakes, Claire, Alahmady, Nada, Koks, Sulev ORCID: 0000-0001-6087-6643, Schumann, Gerald G, Al-Chalabi, Ammar
et al (show 1 more authors) (2020) Frequency and methylation status of selected retrotransposition competent L1 loci in amyotrophic lateral sclerosis. MOLECULAR BRAIN, 13 (1). 154-.


Hunt, Guy P, Grassi, Luigi, Henkin, Rafael, Smeraldi, Fabrizio, Spargo, Thomas P, Kabiljo, Renata, Koks, Sulev ORCID: 0000-0001-6087-6643, Ibrahim, Zina, Dobson, Richard JB, Al-Chalabi, Ammar
et al (show 2 more authors) (2022) GEOexplorer: a webserver for gene expression analysis and visualisation. NUCLEIC ACIDS RESEARCH, 50 (W1). W367-W374.


Koks, Gea, Prans, Ele, Ha, Diep Thi Tran, Ngoc, Bich Thi Ngo, Linh, Nhat Nguyen Hoang, Hue, Minh Thi Tran, Thanh, Cao Ngoc, Thuoc, Doan Phuoc, Xuan, Dung Ho, Binh, Ho Duy
et al (show 3 more authors) (2018) Genetic Interaction Between Two VNTRs in the SLC6A4 Gene Regulates Nicotine Dependence in Vietnamese Men. FRONTIERS IN PHARMACOLOGY, 9. 1398-.


Koks, Sulev ORCID: 0000-0001-6087-6643, Wood, David J, Reimann, Ene, Awiszus, Friedemann, Lohmann, Christoph H, Bertrand, Jessica, Prans, Ele, Maasalu, Katre and Martson, Aare
(2020) The Genetic Variations Associated With Time to Aseptic Loosening After Total Joint Arthroplasty. JOURNAL OF ARTHROPLASTY, 35 (4). pp. 981-988.


Koks, Gea, Prans, Ele, Ho, Xuan D, Duy, Binh H, Tran, Ha DT, Ngo, Ngoc BT, Hoang, Linh NN, Tran, Hue MT, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803
et al (show 1 more authors) (2020) Genetic interaction between two VNTRs in the MAOA gene is associated with the nicotine dependence. EXPERIMENTAL BIOLOGY AND MEDICINE, 245 (8). pp. 733-739.


Eltermaa, Mall, MailiJakobson, , Utt, Meeme, Koks, Sulev ORCID: 0000-0001-6087-6643, Magi, Reedik and Starkopf, Joel
(2019) Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease. BMC RESEARCH NOTES, 12 (1). 759-.


Billingsley, Kimberley, Barbosa, Ines, Bandrés-Ciga, Sara, Quinn, John ORCID: 0000-0003-3551-7803, Bubb, Vivien, Deshpande, Charu, Botia, Juan, Reynolds, Regina, Zhang, David, Simpson, Michael ORCID: 0000-0002-8539-8753
et al (show 8 more authors) (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. BioRxiv. 475111-.


Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2023) A Genome-Wide Screen for the Exonisation of Reference SINE-VNTR-Alus and Their Expression in CNS Tissues of Individuals with Amyotrophic Lateral Sclerosis. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 24 (14). 11548-.


Grover, Sandeep, Kumar Sreelatha, Ashwin Ashok, Pihlstrom, Lasse, Domenighetti, Cloe, Schulte, Claudia, Sugier, Pierre-Emmanuel, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Mohamed, Oceane, Portugal, Berta
et al (show 73 more authors) (2022) Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium. NEUROLOGY, 99 (7). E698-E710.


Jin, Ying, Andersen, Genevieve, Yorgov, Daniel, Ferrara, Tracey M, Ben, Songtao, Brownson, Kelly M, Holland, Paulene J, Birlea, Stanca A, Siebert, Janet, Hartmann, Anke
et al (show 34 more authors) (2016) Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. NATURE GENETICS, 48 (11). pp. 1418-1424.


Koks, Sulev ORCID: 0000-0001-6087-6643
(2023) Genomics of Wolfram Syndrome 1 (WFS1). BIOMOLECULES, 13 (9). 1346-.


Zhytnik, Lidiia, Maasalu, Katre, Duy, Binh Ho, Pashenko, Andrey, Khmyzov, Sergey, Reimann, Ene, Prans, Ele, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2019) IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients. HUMAN GENOMICS, 13 (1). 25-.


Reimann, Ene, Abram, Kristi, Koks, Sulev ORCID: 0000-0001-6087-6643, Kingo, Kulli and Fazeli, Alireza
(2019) Identification of an optimal method for extracting RNA from human skin biopsy, using domestic pig as a model system. SCIENTIFIC REPORTS, 9 (1). 20111-.


Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli
et al (show 260 more authors) (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12). pp. 1091-1102.


Esteki, Masoud Zamani, Viltrop, Triin, Tsuiko, Olga, Tiirats, Airi, Koel, Mariann, Noukas, Margit, Zilina, Olga, Teearu, Katre, Marjonen, Heidi, Kahila, Hanna
et al (show 11 more authors) (2019) In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages. NATURE MEDICINE, 25 (11). 1699-+.


Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2020) An Increased Burden of Highly Active Retrotransposition Competent L1s Is Associated with Parkinson's Disease Risk and Progression in the PPMI Cohort. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 21 (18). E6562-.


Eimre, Margus, Paju, Kalju, Peet, Nadezda, Kadaja, Lumme, Tarrend, Marian, Kasvandik, Sergo, Seppet, Joosep, Ivask, Marilin, Orlova, Elite and Koks, Sulev ORCID: 0000-0001-6087-6643
(2018) Increased Mitochondrial Protein Levels and Bioenergetics in the <i>Musculus Rectus Femoris</i> of Wfs1-Deficient Mice. OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2018. 3175313-.


Asser, Andres, Koks, Sulev ORCID: 0000-0001-6087-6643, Snellman, Anniina, Haaparanta-Solin, Merja, Arponen, Eveliina, Gronroos, Tove, Nairismagi, Jaak, Bergquist, Jonas, Soomets, Ursel, Piip, Piret
et al (show 5 more authors) (2016) Increased striatal VMAT2 binding in mice after chronic administration of methcathinone and manganese. BRAIN RESEARCH, 1652. pp. 97-102.


Zhytnik, Lidiia, Maasalu, Katre, Reimand, Tiia, Binh, Ho Duy, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2020) Inter- and Intrafamilial Phenotypic Variability in Individuals with Collagen-Related Osteogenesis Imperfecta. CTS-CLINICAL AND TRANSLATIONAL SCIENCE, 13 (5). pp. 960-971.


Domenighetti, Cloe, Douillard, Venceslas, Sugier, Pierre-Emmanuel, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj R, Radivojkov-Blagojevic, Milena, Lichtner, Peter
et al (show 70 more authors) (2022) The Interaction between <i>HLA-DRB1</i> and Smoking in Parkinson's Disease Revisited. MOVEMENT DISORDERS, 37 (9). pp. 1929-1937.


Sugier, Pierre-Emmanuel, Lucotte, Elise H, Domenighetti, Cloe M, Law, Matthew, Iles, Mark, Brown, Kevin D, Amos, Christopher J, McKay, James, Hung, Rayjean, Karimi, Mojgan
et al (show 84 more authors) (2023) Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. MOVEMENT DISORDERS, 38 (4). pp. 604-615.


Tsoi, Lam C, Stuart, Philip E, Tian, Chao, Gudjonsson, Johann E, Das, Sayantan, Zawistowski, Matthew, Ellinghaus, Eva, Barker, Jonathan N, Chandran, Vinod, Dand, Nick
et al (show 27 more authors) (2017) Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. NATURE COMMUNICATIONS, 8 (1). 15382-.


Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2022) Locus specific reduction of L1 expression in the cortices of individuals with amyotrophic lateral sclerosis. MOLECULAR BRAIN, 15 (1). 25-.


Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004 and Quinn, John P ORCID: 0000-0003-3551-7803
(2022) Longitudinal intronic RNA-Seq analysis of Parkinson's disease patients reveals disease-specific nascent transcription. Experimental biology and medicine (Maywood, N.J.), 247 (11). p. 15353702221081027.


Planken, Anu, Kurvits, Lille, Reimann, Ene, Kadastik-Eerme, Liis, Kingo, Kulli, Koks, Sulev ORCID: 0000-0001-6087-6643 and Taba, Pille
(2017) Looking beyond the brain to improve the pathogenic understanding of Parkinson's disease: implications of whole transcriptome profiling of Patients' skin. BMC NEUROLOGY, 17 (1). 6-.


Kulkarni, Priya, Harsulkar, Abhay, Martson, Anne-Grete, Suutre, Siim, Martson, Aare ORCID: 0000-0001-6478-1959 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2022) Mast Cells Differentiated in Synovial Fluid and Resident in Osteophytes Exalt the Inflammatory Pathology of Osteoarthritis. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (1). 541-.


Reemann, Paula, Reimann, Ene, Ilmjarv, Sten, Porosaar, Orm, Silm, Helgi, Jaks, Viljar, Vasar, Eero, Kingo, Kulli and Koks, Sulev ORCID: 0000-0001-6087-6643
(2017) Melanocytes in the Skin - Comparative Whole Transcriptome Analysis of Main Skin Cell Types (vol 9, e115717, 2014). PLOS ONE, 12 (3). e0173792-.


Billingsley, Kimberley J, Barbosa, Ines A, Bandres-Ciga, Sara, Quinn, John P ORCID: 0000-0003-3551-7803, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Deshpande, Charu, Botia, Juan A, Reynolds, Regina H, Zhang, David, Simpson, Michael A
et al (show 136 more authors) (2019) Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. NPJ PARKINSONS DISEASE, 5 (1). 8-.


Koks, Sulev ORCID: 0000-0001-6087-6643, Dogan, Soner, Tuna, Bilge Guvenc, Gonzalez-Navarro, Herminia, Potter, Paul and Vandenbroucke, Roosmarijn E
(2016) Mouse models of ageing and their relevance to disease. MECHANISMS OF AGEING AND DEVELOPMENT, 160. pp. 41-53.


Reimann, Ene, Lattekivi, Freddy, Keermann, Maris, Abram, Kristi, Koks, Sulev ORCID: 0000-0001-6087-6643, Kingo, Kulli and Fazeli, Alireza
(2019) Multicomponent Biomarker Approach Improves the Accuracy of Diagnostic Biomarkers for Psoriasis Vulgaris. ACTA DERMATO-VENEREOLOGICA, 99 (13). pp. 1258-1265.


Waszczykowska, Arleta, Zmyslowska, Agnieszka, Braun, Marcin, Ivask, Marilin, Koks, Sulev ORCID: 0000-0001-6087-6643, Jurowski, Piotr and Mlynarski, Wojciech
(2020) Multiple Retinal Anomalies in Wfs1-Deficient Mice. DIAGNOSTICS, 10 (9). E607-.


Binh, Ho Duy, Zhytnik, Lidiia, Maasalu, Katre, Kandla, Ivo, Prans, Ele, Reimann, Ene, Martson, Aare and Koks, Sulev ORCID: 0000-0001-6087-6643
(2016) Mutation analysis of the <i>COL1A1</i> and <i>COL1A2</i> genes in Vietnamese patients with osteogenesis imperfecta. HUMAN GENOMICS, 10 (1). 27-.


Zhytnik, Lidiia, Maasalu, Katre, Reimann, Ene, Prans, Ele, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2017) Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients. HUMAN GENOMICS, 11 (1). 19-.


Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail L, Singleton, Lewis M, Bubb, Vivien J ORCID: 0000-0003-2763-7004 and Quinn, John P ORCID: 0000-0003-3551-7803
(2022) Non-reference genome transposable elements (TEs) have a significant impact on the progression of the Parkinson's disease. EXPERIMENTAL BIOLOGY AND MEDICINE, 247 (18). pp. 1680-1690.


Minh, Son Nguyen, Ho, Duy Binh, Khac, Minh Nguyen, Maasalu, Katre, Koks, Sulev ORCID: 0000-0001-6087-6643, Martson, Aare, Saag, Mare and Jagomagi, Triin
(2017) Occlusal features and need for orthodontic treatment in persons with osteogenesis imperfecta. CLINICAL AND EXPERIMENTAL DENTAL RESEARCH, 3 (1). pp. 19-24.


Zhytnik, Lidiia, Duy, Binh Ho, Eekhoff, Marelise, Wisse, Lisanne, Pals, Gerard, Reimann, Ene, Koks, Sulev ORCID: 0000-0001-6087-6643, Martson, Aare, Maugeri, Alessandra, Maasalu, Katre
et al (show 1 more authors) (2022) Phenotypic Variation in Vietnamese Osteogenesis Imperfecta Patients Sharing a Recessive <i>P3H1</i> Pathogenic Variant. GENES, 13 (3). 407-.


Traks, Tanel, Keermann, Maris, Prans, Ele, Karelson, Maire, Loite, Ulvi, Koks, Gea, Silm, Helgi, Koks, Sulev ORCID: 0000-0001-6087-6643 and Kingo, Kulli
(2019) Polymorphisms in IL36G gene are associated with plaque psoriasis. BMC MEDICAL GENETICS, 20 (1). 10-.


Eimre, Margus, Kasvandik, Sergo, Ivask, Marilin and Koks, Sulev ORCID: 0000-0001-6087-6643
(2018) Proteomic dataset of wolframin-deficient mouse heart and skeletal muscles. DATA IN BRIEF, 21. pp. 616-619.


Koks, Sulev ORCID: 0000-0001-6087-6643, Keermann, Maris, Reimann, Ene, Prans, Ele, Abram, Kristi, Silm, Helgi, Koks, Gea and Kingo, Kulli
(2016) Psoriasis-Specific RNA Isoforms Identified by RNA-Seq Analysis of 173,446 Transcripts. FRONTIERS IN MEDICINE, 3 (OCT). 46-.


Zhytnik, Lidiia, Maasalu, Katre, Reimann, Ene, Martson, Aare and Koks, Sulev ORCID: 0000-0001-6087-6643
(2020) RNA sequencing analysis reveals increased expression of interferon signaling genes and dysregulation of bone metabolism affecting pathways in the whole blood of patients with osteogenesis imperfecta. BMC MEDICAL GENOMICS, 13 (1). 177-.


Ivask, Marilin, Hugill, Alison and Koks, Sulev ORCID: 0000-0001-6087-6643
(2016) RNA-sequencing of WFS1-deficient pancreatic islets. PHYSIOLOGICAL REPORTS, 4 (7). e12750-.


Lindholm, Dan, Korhonen, Laura, Eriksson, Ove and Koks, Sulev ORCID: 0000-0001-6087-6643
(2017) Recent Insights into the Role of Unfolded Protein Response in ER Stress in Health and Disease. FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 5 (MAY). 48-.


Fröhlich, Alexander, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2023) Reference LINE-1 insertion polymorphisms correlate with Parkinson's disease progression and differential transcript expression in the PPMI cohort. Scientific reports, 13 (1). p. 13857.


Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2021) Reference SVA insertion polymorphisms are associated with Parkinson's Disease progression and differential gene expression. NPJ PARKINSONS DISEASE, 7 (1). 44-.


Pfaff, Abigail, Bubb, Vivien ORCID: 0000-0003-2763-7004, Quinn, John and Koks, Sulev ORCID: 0000-0001-6087-6643
(2020) Reference SVA insertion polymorphisms are associated with dopaminergic degeneration in Parkinson’s Disease and differential gene expression in the PPMI cohort. Unknown.


Kurvits, Lille, Reimann, Ene, Kadastik-Eerme, Liis, Truu, Laura, Kingo, Kulli, Erm, Triin, Koks, Sulev ORCID: 0000-0001-6087-6643, Taba, Pille and Planken, Anu
(2019) Serum Amyloid Alpha Is Downregulated in Peripheral Tissues of Parkinson's Disease Patients. FRONTIERS IN NEUROSCIENCE, 13 (JAN). 13-.


Gorecki, Anastazja M, Bakeberg, Megan C, Theunissen, Frances, Kenna, Jade E, Hoes, Madison E, Pfaff, Abigail L, Akkari, P Anthony, Dunlop, Sarah A, Koks, Sulev ORCID: 0000-0001-6087-6643, Mastaglia, Frank L
et al (show 1 more authors) (2020) Single Nucleotide Polymorphisms Associated With Gut Homeostasis Influence Risk and Age-at-Onset of Parkinson's Disease. FRONTIERS IN AGING NEUROSCIENCE, 12. 603849-.


Koks, Gea, Fischer, Krista and Koks, Sulev ORCID: 0000-0001-6087-6643
(2017) Smoking-related general and cause-specific mortality in Estonia. BMC PUBLIC HEALTH, 18 (1). 34-.


Asser, Andres, Hikima, Atsuko, Raki, Mari, Bergstrom, Kim, Rose, Sarah, Juurmaa, Julius, Krispin, Villem, Muldmaa, Mari, Lilles, Stella, Raetsep, Hanna
et al (show 4 more authors) (2020) Subacute administration of both methcathinone and manganese causes basal ganglia damage in mice resembling that in methcathinone abusers. JOURNAL OF NEURAL TRANSMISSION, 127 (5). pp. 707-714.


Kulkarni, Priya, Srivastava, Vanshika, Tootsi, Kaspar, Electricwala, Ali, Kharat, Avinash, Bhonde, Ramesh, Koks, Sulev ORCID: 0000-0001-6087-6643, Martson, Aare and Harsulkar, Abhay
(2022) Synovial Fluid in Knee Osteoarthritis Extends Proinflammatory Niche for Macrophage Polarization. CELLS, 11 (24). 4115-.


Ingale, Dhanashri, Kulkarni, Priya, Electricwala, Ali, Moghe, Alpana, Kamyab, Sara, Jagtap, Suresh, Martson, Aare, Koks, Sulev ORCID: 0000-0001-6087-6643 and Harsulkar, Abhay
(2021) Synovium-Synovial Fluid Axis in Osteoarthritis Pathology: A Key Regulator of the Cartilage Degradation Process. GENES, 12 (7). 989-.


Otero-Ferrer, Francisco, Lattekivi, Freddy, Ord, James, Reimann, Ene, Koks, Sulev ORCID: 0000-0001-6087-6643, Izquierdo, Marisol, Holt, William Vincent and Fazeli, Alireza
(2020) Time-critical influences of gestational diet in a seahorse model of male pregnancy. JOURNAL OF EXPERIMENTAL BIOLOGY, 223 (3). jeb210302-.


Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004 and Quinn, John P ORCID: 0000-0003-3551-7803
(2021) Transcript Variants of Genes Involved in Neurodegeneration Are Differentially Regulated by the APOE and MAPT Haplotypes. GENES, 12 (3). 423-.


Koks, Sulev ORCID: 0000-0001-6087-6643, Pfaff, Abigail, Bubb, Vivien and Quinn, John ORCID: 0000-0003-3551-7803
(2021) Transcript Variants of Genes Involved in Neurodegeneration Are Differentially Regulated by the Apoe and Mapt Haplotypes. Genes.


Krishnan, Vidya S and Koks, Sulev ORCID: 0000-0001-6087-6643
(2022) Transcriptional Basis of Psoriasis from Large Scale Gene Expression Studies: The Importance of Moving towards a Precision Medicine Approach. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (11). 6130-.


Maasalu, Katre, Laius, Ott, Zhytnik, Lidiia, Koks, Sulev ORCID: 0000-0001-6087-6643, Prans, Ele, Reimann, Ene and Martson, Aare
(2017) Transcriptional landscape analysis identifies differently expressed genes involved in follicle-stimulating hormone induced postmenopausal osteoporosis. EXPERIMENTAL BIOLOGY AND MEDICINE, 242 (2). pp. 203-213.


Lattekivi, Freddy, Koks, Sulev ORCID: 0000-0001-6087-6643, Keermann, Maris, Reimann, Ene, Prans, Ele, Abram, Kristi, Silm, Helgi, Koks, Gea and Kingo, Kulli
(2018) Transcriptional landscape of human endogenous retroviruses (HERVs) and other repetitive elements in psoriatic skin. SCIENTIFIC REPORTS, 8 (1). 4358-.


Fröhlich, Alexander, Pfaff, Abigail L, Bubb, Vivien J ORCID: 0000-0003-2763-7004, Quinn, John P ORCID: 0000-0003-3551-7803 and Koks, Sulev ORCID: 0000-0001-6087-6643
(2023) Transcriptomic profiling of cerebrospinal fluid identifies ALS pathway enrichment and RNA biomarkers in MND individuals. Experimental biology and medicine (Maywood, N.J.), 248 (23). p. 15353702231209427.


Laius, Ott, Pisarev, Heti, Maasalu, Katre, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2017) Trends in and relation between hip fracture incidence and osteoporosis medication utilization and prices in Estonia in 2004-2015. ARCHIVES OF OSTEOPOROSIS, 12 (1). 48-.


Marriott, Heather, Kabiljo, Renata, Hunt, Guy P, Khleifat, Ahmad Al, Jones, Ashley, Troakes, Claire, Project MinE ALS Sequencing Consortium, , TargetALS Sequencing Consortium, , Pfaff, Abigail L, Quinn, John P ORCID: 0000-0003-3551-7803
et al (show 5 more authors) (2023) Unsupervised machine learning identifies distinct ALS molecular subtypes in post-mortem motor cortex and blood expression data. Acta neuropathologica communications, 11 (1). 208-.


Rothzerg, Emel, Ho, Xuan Dung, Xu, Jiake, Wood, David, Maertson, Aare and Koks, Sulev ORCID: 0000-0001-6087-6643
(2021) Upregulation of 15 Antisense Long Non-Coding RNAs in Osteosarcoma. GENES, 12 (8). 1132-.


Laius, Ott, Maasalu, Katre, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2016) Use of drugs against osteoporosis in the Baltic countries during 2010-2014. MEDICINA-LITHUANIA, 52 (5). pp. 315-320.


Dewhurst, Robert E, Heinrich, Tatjana, Watt, Paul, Ostergaard, Paul, Marimon, Jose M, Moreira, Mariana, Houldsworth, Philip E, Rudrum, Jack D, Wood, David and Koks, Sulev ORCID: 0000-0001-6087-6643
(2022) Validation of a rapid, saliva-based, and ultra-sensitive SARS-CoV-2 screening system for pandemic-scale infection surveillance. SCIENTIFIC REPORTS, 12 (1). 5936-.


Marshall, Jack NG, Lopez, Ana Illera, Pfaff, Abigail L, Koks, Sulev ORCID: 0000-0001-6087-6643, Quinn, John P ORCID: 0000-0003-3551-7803 and Bubb, Vivien J ORCID: 0000-0003-2763-7004
(2021) Variable number tandem repeats - Their emerging role in sickness and health. EXPERIMENTAL BIOLOGY AND MEDICINE, 246 (12). pp. 1368-1376.


Ho, Duy Binh, Maasalu, Katre, Dung, Vu Chi, Bich Ngoc, Can T, Ton, That Hung, Nam, Tran V, Thanh Nhan, Le N, Prans, Ele, Reimann, Ene, Zhytnik, Lidiia
et al (show 2 more authors) (2017) The clinical features of osteogenesis imperfecta in Vietnam. INTERNATIONAL ORTHOPAEDICS, 41 (1). pp. 21-29.


Tatte, Kai, Pagani, Luca, Pathak, Ajai K, Koks, Sulev ORCID: 0000-0001-6087-6643, Binh, Ho Duy, Xuan, Dung Ho, Sultana, Gazi Nurun Nahar, Sharif, Mohd Istiaq, Asaduzzaman, Md, Behar, Doron M
et al (show 5 more authors) (2019) The genetic legacy of continental scale admixture in Indian Austroasiatic speakers (vol 9, 3818, 2019). SCIENTIFIC REPORTS, 9 (1). 6104-.


Tatte, Kai, Pagani, Luca, Pathak, Ajai K, Koks, Sulev ORCID: 0000-0001-6087-6643, Binh, Ho Duy, Xuan, Dung Ho, Sultana, Gazi Nurun Nahar, Sharif, Mohd Istiaq, Asaduzzaman, Md, Behar, Doron M
et al (show 5 more authors) (2019) The genetic legacy of continental scale admixture in Indian Austroasiatic speakers. SCIENTIFIC REPORTS, 9 (1). 3818-.


Tiirats, Airi, Viltrop, Triin, Noukas, Margit, Reimann, Ene, Salumets, Andres and Koks, Sulev ORCID: 0000-0001-6087-6643
(2016) <i>C14orf132</i> gene is possibly related to extremely low birth weight. BMC GENETICS, 17 (1). 132-.


Zhytnik, Lidiia, Maasalu, Katre, Pashenkos, Andrey, Khmyzovs, Sergey, Reimann, Ene, Prans, Ele, Koks, Sulev ORCID: 0000-0001-6087-6643 and Martson, Aare
(2019) <i>COL1A1/2</i> Pathogenic Variants and Phenotype Characteristics in Ukrainian Osteogenesis Imperfecta Patients. FRONTIERS IN GENETICS, 10 (JUL). 722-.


Fernandez-Santiago, Ruben, Martin-Flores, Nuria, Antonelli, Francesca, Cerquera, Catalina, Moreno, Veronica, Bandres-Ciga, Sara, Manduchi, Elisabetta, Tolosa, Eduard, Singleton, Andrew B, Moore, Jason H
et al (show 152 more authors) (2019) <i>SNCA</i> and <i>mTOR</i> Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. MOVEMENT DISORDERS, 34 (9). pp. 1333-1344.


Bakeberg, Megan C, Gorecki, Anastazja M, Pfaff, Abigail L, Hoes, Madison E, Koks, Sulev ORCID: 0000-0001-6087-6643, Akkari, P Anthony, Mastaglia, Frank L and Anderton, Ryan S
(2021) <i>TOMM40 '523'</i> poly-T repeat length is a determinant of longitudinal cognitive decline in Parkinson's disease. NPJ PARKINSONS DISEASE, 7 (1). 56-.


Bakeberg, Megan C, Hoes, Madison E, Gorecki, Anastazja M, Theunissen, Frances, Pfaff, Abigail L, Kenna, Jade E, Plunkett, Kai, Koks, Sulev ORCID: 0000-0001-6087-6643, Akkari, P Anthony, Mastaglia, Frank L
et al (show 1 more authors) (2021) The <i>TOMM40 '523'</i> polymorphism in disease risk and age of symptom onset in two independent cohorts of Parkinson's disease. SCIENTIFIC REPORTS, 11 (1). 6363-.


Marshall, Jack NG, Fröhlich, Alexander, Li, Li, Pfaff, Abigail L, Middlehurst, Ben, Spargo, Thomas P, Iacoangeli, Alfredo, Lang, Bing, Al-Chalabi, Ammar, Koks, Sulev ORCID: 0000-0001-6087-6643
et al (show 2 more authors) (2022) A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene <i>CFAP410</i> correlates with differential isoform expression. Frontiers in molecular neuroscience, 15. p. 954928.


Marjonen, Heidi, Auvinen, Pauliina, Kahila, Hanna, Tsuiko, Olga, Koks, Sulev ORCID: 0000-0001-6087-6643, Tiirats, Airi, Viltrop, Triin, Tuuri, Timo, Soderstrom-Anttila, Viveca, Suikkari, Anne-Maria
et al (show 3 more authors) (2018) rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology. CLINICAL EPIGENETICS, 10 (1). 80-.

This list was generated on Sat Mar 16 04:10:57 2024 GMT.