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Publications
| 2024 |
Genotype imputation in human genomic studies
Berdnikova AA, Zorkoltseva IV, Tsepilov YA, Elgaeva EE
[Vavilov journal of genetics and breeding]
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Imputed Genotypes Versus Sequenced Genotypes
for the Association Analysis of Rare Variants
I. V. Zorkoltsevaa, T. I. Axenovicha, Y. A. Tsepilov
[RUSS J GENET+]
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| 2023 |
Multi-Trait Exome-Wide Association Study of Back Pain-Related Phenotypes
Zorkoltseva IV
Elgaeva EE
Belonogova NM
Kirichenko AV
Svishcheva GR
Freidin MB
Williams FMK
Suri P
Tsepilov YA
Axenovich TI
[Genes]
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| 2022 |
In silico genome-wide gene-based association analysis reveals new genes predisposing to coronary artery disease
Zorkoltseva I, Shadrina A, Belonogova N, Kirichenko A, Tsepilov Y, Axenovich T.
[CLIN GENET]
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sumSTAAR: A flexible framework for gene-based association studies using GWAS summary statistics
Nadezhda M. Belonogova, Gulnara R. Svishcheva, Anatoly V. Kirichenko, Irina V. Zorkoltseva, Yakov A. Tsepilov, Tatiana I. Axenovich
[PLOS COMPUT BIOL]
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| 2021 |
Gene‑based association analysis identifes 190 genes affecting neuroticism
Nadezhda M. Belonogova
IrinaV. Zorkoltseva
YakovA.Tsepilov
Tatiana I.Axenovich
[SCI REP-UK]
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ОЦЕНКА ЧИСЛА ГЕНОВ, ПОЛИМОРФИЗМ КОТОРЫХ ВЛИЯЕТ НА УРОВЕНЬ НЕЙРОТИЗМА
Аксенович ТИ, Белоногова НМ, Зоркольцева ИВ, Цепилов ЯА
[Генетика]
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| 2019 |
Gene-based association tests using GWAS summary statistics
Gulnara R Svishcheva, Nadezhda M Belonogova, Irina V Zorkoltseva, Anatoly V Kirichenko, Tatiana I Axenovich
[BIOINFORMATICS]
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In silico поиск генов, контролирующих ишемическую болезнь сердца
Зоркольцева И.В., Белоногова Н.М., Свищёва Г.Р., Кириченко А.В., Аксенович Т.И.
[Vavilov journal of genetics and breeding]
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| 2018 |
A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy
Claudia Tamar Silva
Irina Zorkoltseva
Marieke Niemeijer
Marten E. van den Berg
Najaf Amin
Ayşe Demirkan
Elisa van Leeuwen
Adriana I. Iglesias
Laura B. Piñeros-Hernández
Carlos M. Restrepo
Jan A. Kors
Anatoly Kirichenko
Rob Willemsen
Ben A. Oostra
Bruno H. Stricker
André G. Uitterlinden
Tatiana I. Axenovich
Cornelia M. van Duijn
Aaron Isaacs
[BMC MED GENOMICS]
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Использование генотипов распространенных вариантов для полногеномного регионального анализа ассоциаций
А. Кириченко
И. Зоркольцева
Н. Белоногова
Т. Аксенович
[Генетика]
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| 2017 |
Non-synonymous variation in NKPD1 increases depressive symptoms in the European populations
Najaf Amin, Nadezhda M. Belonogova, Olivera Jovanova, Rutger W.W. Brouwer, Jeroen G.J. van Rooij, Mirjam C.G.N. van den Hout, Gulnara R. Svishcheva, Robert Kraaij, Irina V. Zorkoltseva, Anatoly V. Kirichenko, Albert Hofman, André G. Uitterlinden, Wilfred F.J. van IJcken, Henning Tiemeier, Tatiana I. Axenovich, Cornelia M. van Duijn
[BIOL PSYCHIAT]
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| 2016 |
A combined linkage and exome sequencing analysis for electrocardiogram parameters in the Erasmus Rucphen Family study.
Claudia T. Silva, Irina Zorkoltseva, Najaf Amin, Ayse Demirkan, Elisabeth M. Van Leeuwen, Jan Kors, Marten van den Berg, Bruno Stricker, André Uitterlinden, Anatoly Kirichenko, Jacqueline C.M. Witteman, Rob Willemsen, Ben Oostra, Tatiana Axenovich, Cornelia M. Van Duijn, Aaron Isaacs
[Frontiers in Genetics]
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| 2014 |
Изучение наследственных форм тугоухости / глухоты в Республике Тыва. Cообщение I. Эпидемиология нарушений слуха в Республике Тыва.
Бады-Хоо М.С., Посух О.Л., Зоркольцева И.В., Скиданова О.В., Барашков Н.А., Омзар О.С., Монгуш Р.Ш., Бамба О.М., Тукар В.М., Зыцарь М.В., Михальская В.Ю.
[Медицинская генетика]
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| 2013 |
Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions
Amin N, Hottenga JJ, Hansell NK, Janssens AC, de Moor MH, Madden PA, Zorkoltseva IV, Penninx BW, Terracciano A, Uda M, Tanaka T, Esko T, Realo A, Ferrucci L, Luciano M, Davies G, Metspalu A, Abecasis GR, Deary IJ, Raikkonen K, Bierut LJ, Costa PT, Saviouk V, Zhu G, Kirichenko AV, Isaacs A, Aulchenko YS, Willemsen G, Heath AC, Pergadia ML, Medland SE, Axenovich TI, de Geus E, Montgomery GW, Wright MJ, Oostra BA, Martin NG, Boomsma DI, van Duijn CM.
[EUR J HUM GENET]
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| 2012 |
A genome-wide linkage study of individuals with high scores on NEO personality traits.
Amin N, Schuur M, Gusareva ES, Isaacs A, Aulchenko YS, Kirichenko AV, Zorkoltseva IV, Axenovich TI, Oostra BA, Janssens AC, van Duijn CM.
[MOL PSYCHIATR]
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GADS software for parametric linkage analysis of quantitative traits distributed as a point-mass mixture.
Axenovich TI, Zorkoltseva IV.
[COMPUT BIOL CHEM]
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Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations
Demirkan A, van Duijn CM, Ugocsai P, Isaacs A, Pramstaller PP, Liebisch G, Wilson JF, Johansson Å, Rudan I, Aulchenko YS, Kirichenko AV, Janssens AC, Jansen RC, Gnewuch C, Domingues FS, Pattaro C, Wild SH, Jonasson I, Polasek O, Zorkoltseva IV, Hofman A, Karssen LC, Struchalin M, Floyd J, Igl W, Biloglav Z, Broer L, Pfeufer A, Pichler I, Campbell S, Zaboli G, Kolcic I, Rivadeneira F, Huffman J, Hastie ND, Uitterlinden A, Franke L, Franklin CS, Vitart V; DIAGRAM Consortium, Nelson CP, Preuss M; CARDIoGRAM Consortium, Bis JC, O'Donnell CJ, Franceschini N; CHARGE Consortium, Witteman JC, Axenovich T, Oostra BA, Meitinger T, Hicks AA, Hayward C, Wright AF, Gyllensten U, Campbell H, Schmitz G; EUROSPAN consortium
[PLOS GENET]
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Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2
Ibrahim-Verbaas CA, Zorkoltseva IV, Amin N, Schuur M, Coppus AM, Isaacs A, Aulchenko YS, Breteler MM, Ikram MA, Axenovich TI, Verbeek MM, van Swieten JC, Oostra BA, van Duijn CM.
[HUM GENET]
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| 2011 |
Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population
Axenovich T, Zorkoltseva I, Belonogova N, van Koolwijk L, Borodin P, Kirichenko A, Babenko V, Ramdas W, Amin N, Despriet D, Vingerling J, Lemij H, Oostra BA, Klaver C, Aulchenko Y, van Duijn C.
[J MED GENET]
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| 2010 |
A Genome-Wide Screen for Depression in Two Independent Dutch Populations
Schol-Gelok S, Janssens AC, Tiemeier H, Liu F, Lopez-Leon S, Zorkoltseva IV, Axenovich TI, van Swieten JC, Uitterlinden AG, Hofman A, Aulchenko YS, Oostra BA, van Duijn CM.
[BIOL PSYCHIAT]
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Genetic Architecture of Plasma Adiponectin Overlaps With the Genetics of Metabolic Syndrome-Related Traits
Henneman P, Aulchenko YS, Frants RR, Zorkoltseva IV, Zillikens MC, Frolich M, Oostra BA, van Dijk KW, van Duijn CM.
[DIABETES CARE]
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Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene OBESITY
Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Floyd J, Hastie N, Knott S, Lauc G, Pichler I, Rotim K, Wild SH, Zorkoltseva IV, Wilson JF, Rudan I, Campbell H, Pattaro C, P
[OBESITY]
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Ped_Outlier software for automatic identification of within-family outliers
Zorkoltseva IV, Aulchenko YS, van Duijn CM, Axenovich TI.
[COMPUT BIOL CHEM]
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The apolipoprotein E gene and its age-specific effects on cognitive function
Liu F, Pardo LM, Schuur M, Sanchez-Juan P, Isaacs A, Sleegers K, de Koning I, Zorkoltseva IV, Axenovich TI, Witteman JC, Janssens AC, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM.
[NEUROBIOL AGING]
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| 2009 |
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Dunlop MG, Floyd J, Hastie N, Hofman A, Knott S, Kolcic I, Pichler I, Polasek O, Rivadeneira F, Tenesa A, Uitterlinden AG, Wi
[HUM MOL GENET]
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Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations
Hicks AA, Pramstaller PP, Johansson A, Vitart V, Rudan I, Ugocsai P, Aulchenko Y, Franklin CS, Liebisch G, Erdmann J, Jonasson I, Zorkoltseva IV, Pattaro C, Hayward C, Isaacs A, Hengstenberg C, Campbell S, Gnewuch C, Janssens AC, Kirichenko AV, König
[PLOS GENET]
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Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population
Axenovich T.I., Zorkoltseva I.V., Belonogova N.M. Struchalin, MV; Kirichenko, AV); Kayser, M); Oostra, BA; van Duijn, CM; Aulchenko, YS .
[HUM GENET]
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| 2008 |
Breaking loops in large complex pedigrees
Axenovich TI, Zorkoltseva IV, Liu F, Kirichenko AV, Aulchenko YS
[HUM HERED]
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The apolipoprotein E gene and its age-specific effects on cognitive function
Liu F, Pardo LM, Schuur M, Sanchez-Juan P, Isaacs A, Sleegers K, de Koning I, Zorkoltseva IV, Axenovich TI, Witteman JC, Janssens AC, van Swieten JC, Aulchenko YS, Oostra BA, van Duijn CM.
[NEUROBIOL AGING]
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| 2007 |
Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes
van Rijn MJ, Schut AF, Aulchenko YS, Deinum J, Sayed-Tabatabaei FA, Yazdanpanah M, Isaacs A, Axenovich TI, Zorkoltseva IV, Zillikens MC, Pols HA, Witteman JC, Oostra BA, van Duijn CM
[J HYPERTENS]
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Inheritance of litter size at birth in farmed arctic foxes (Alopex lagopus, Canidae, Carnivora)
Axenovich TI, Zorkoltseva IV, Akberdin IR, Beketov SV, Kashtanov SN, Zakharov IA, Borodin PM.
[HEREDITY]
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Полиморфизм гена рецепторного антагониста интерлейкина-1 у пришлого и коренного населения Кемеровской области
Шабалдин, А.В.; Остапцева, А.В.; Ахматьянова, В.Р.; Минина, В.И.; Глушкова, О.А.; Макарченко, О.С.; Филипенко, М.Л.; Шабалдина , Е.В.; Дружинин, В.Г.; Зоркольцева, И.В.
[Иммунология]
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| 2006 |
Changes in litter size in Kerry Blue Terrier dogs with abnormal dentition
Zorkoltseva I.V., Akberdin I.R., Kulikova A.V, Knyazev S.V, Borodin P.M, Axenovich T.I.
[RUSS J GENET+]
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Polymorphism of aggrecan gene in families with idiopathic scoliosis
Sharipov RN, Zaidman AM, Zorkol'tseva IV, Aksenovich TI, Dymshits GM.
[Molecular Biology]
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Polymorphism of dental formula and segregation of its variants in a pedigree of kerry blue terrier dogs
Aksenovich TI, Kulikova AV, Kniazev SP, Zorkal'tseva IV, Borodin PM.
[RUSS J GENET+]
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Сравнительный анализ полиморфизма VNTR аллелей гена фенилаланингидроксилазы в выборке населения г. Новосибирска и телеутов в Кемеровской области
Воронина, Е. Н.; Шабалдин, А. В.; Филипенко, М. Л.; Глушков, А. Н.; Гордеева, Л. А.; Зоркольцева, И. В.; Глушкова, О. А.; Ларин, С. А.
[Сибирский медицинский журнал]
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