Institution · Asper Biotech (Estonia)
Most cited papers from Asper Biotech (Estonia)
What are the most cited papers from Asper Biotech (Estonia)?
The most cited paper from Asper Biotech (Estonia) is "A first-generation linkage disequilibrium map of human chromosome 22" (Elisabeth Dawson et al., 2002), with 405 citations. Next come "Genotyping microarray (gene chip) for theABCR(ABCA4) gene" (241) and "Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles" (178).
Showing 50 of 66 papers. Every paper is listed.
| # | Paper | ||
|---|---|---|---|
| 1 | A first-generation linkage disequilibrium map of human chromosome 22 Elisabeth Dawson et al. · Nature | 10 Jul 2002 | 405 |
| 2 | Genotyping microarray (gene chip) for theABCR(ABCA4) gene Kaie Jaakson, Jana Zernant, Maigi Külm et al. · Human Mutation | 25 Sep 2003 | 241 |
| 3 | Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles Jana Zernant, Maigi Ku ̈lm, Sharola Dharmaraj et al. · Investigative Ophthalmology & Visual Science | 25 Aug 2005 | 178 |
| 4 | Development of a genotyping microarray for Usher syndrome Cremers, F P M, et al, Fleischhauer, J C et al. · Zurich Open Repository and Archive (University of Zurich) | 2007 | 106 |
| 5 | Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene Neeme Tõnisson, Jana Zernant, Ants Kurg et al. · Proceedings of the National Academy of Sciences | 16 Apr 2002 | 98 |
| 6 | Association study of 90 candidate gene polymorphisms in panic disorder Eduard Maron, Tiit Nikopensius, Sulev K ks et al. · Psychiatric Genetics | 18 Feb 2005 | 92 |
| 7 | Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-up Phyllis Gardner, Eneli Oitmaa, Anna H. Messner et al. · PEDIATRICS | Sep 2006 | 71 |
| 8 | Microarray-Based Mutation Analysis of 183 Spanish Families with Usher Syndrome Teresa Jaijo, Elena Aller, Gema García‐García et al. · Investigative Ophthalmology & Visual Science | 25 Feb 2010 | 64 |
| 9 | Genotyping Microarray for CSNB-Associated Genes Christina Zeitz et al. · Investigative Ophthalmology & Visual Science | Dec 2009 | 64 |
| 10 | Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray. Federica Gemignani, Chiara Perra, Stefano Landi et al. · PubMed | Nov 2002 | 62 |
| 11 | Reliable Detection of β-Thalassemia and G6PD Mutations by a DNA Microarray Federica Gemignani, Chiara Perra, Stefano Landi et al. · Clinical Chemistry | Nov 2002 | 60 |
| 12 | A Novel Mutation and Phenotypes in Phosphodiesterase 6 Deficiency Stephen H. Tsang, Irena Tsui, Chai Lin Chou et al. · American Journal of Ophthalmology | 7 Sep 2008 | 54 |
| 13 | Analysis of SNP profiles in patients with major depressive disorder Sulev Kõks, Tiit Nikopensius, Kati Koido et al. · The International Journal of Neuropsychopharmacology | Jun 2005 | 50 |
| 14 | Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders Kati Koido, Sulev Kõks, Tiit Nikopensius et al. · The International Journal of Neuropsychopharmacology | 19 Apr 2005 | 50 |
| 15 | Genetic assessment following increased nuchal translucency and normal karyotype Eugene Pergament, Christina M. L. Alamillo, Katrin Sak et al. · Prenatal Diagnosis | 15 Feb 2011 | 48 |
| 16 | Mutational Screening of LCA Genes Emphasizing RPE65 in South Indian Cohort of Patients Anshuman Verma, Perumalsamy Vijayalakshmi, Shashikant B Shetty et al. · PLoS ONE | 16 Sep 2013 | 47 |
| 17 | Genotyping Microarray for the Detection of More Than 200 CFTR Mutations in Ethnically Diverse Populations Iris Schrijver, Eneli Oitmaa, Andres Metspalu et al. · Journal of Molecular Diagnostics | Aug 2005 | 44 |
| 18 | Arrayed primer extension technology simplifies mutation detection in Bardet–Biedl and Alström syndrome Inés Pereiro, Bethan E. Hoskins, Jan D. Marshall et al. · European Journal of Human Genetics | 15 Dec 2010 | 37 |
| 19 | Evaluation of the 124-plex SNP typing microarray for forensic testing Kaarel Krjutškov, Triin Viltrop, Priit Palta et al. · Forensic Science International Genetics | 16 May 2009 | 35 |
| 20 | Fluoride‐Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension Diana C. Knapp, Saulius Serva, Jennifer D’Onofrio et al. · Chemistry - A European Journal | 3 Feb 2011 | 33 |
| 21 | Molecular epidemiology of Usher syndrome in Italy. Diego Vozzi, Anu Aaspõllu, Emmanouil Athanasakis et al. · PubMed | 2011 | 31 |
| 22 | Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease Lucie Gojová, Eva Jansová, Maigi Külm et al. · Clinical Genetics | 7 Apr 2008 | 30 |
| 23 | A polymer Lab-on-a-Chip for genetic analysis using the arrayed primer extension on microarray chips Simone Luigi Marasso, Domenico Mombello, Matteo Cocuzza et al. · Biomedical Microdevices | 15 May 2014 | 29 |
| 24 | Li2B4O7:Mn for dosimetry applications: traps and mechanisms; pp. 279–295 Arno Ratas, Mikhail I. Danilkin, Mihkel Kerikmäe et al. · Proceedings of the Estonian Academy of Sciences | 16 Nov 2012 | 28 |
| 25 | Cross-Clade Protection Induced by Human Immunodeficiency Virus-1 DNA Immunogens Expressing Consensus Sequences of Multiple Genes and Epitopes From Subtypes A, B, C, and FGH Maria Malm, Erik Rollman, Mart Ustav et al. · Viral Immunology | Dec 2005 | 28 |
| 26 | Associations Between Milk Performance Traits in Holstein Cows and 16 Candidate SNPs Identified by Arrayed Primer Extension (APEX) Microarray Stanisław Kamiński, P. Brym, Anna Ruść et al. · Animal Biotechnology | 17 Apr 2006 | 25 |
| 27 | Carrier of R14W in Carbonic Anhydrase IV Presents Bothnia Dystrophy Phenotype Caused by Two Allelic Mutations inRLBP1 Linda Ko ̈hn, Marie S. I. Burstedt, Frida Jönsson et al. · Investigative Ophthalmology & Visual Science | 25 Jun 2008 | 22 |
| 28 | Can coverage factor 2 be interpreted as an equivalent to 95% coverage level in uncertainty estimation? Two case studies Martin Vilbaste, Georgi Slavin, Olev Saks et al. · Measurement | 18 Dec 2009 | 21 |
| 29 | A quality assessment survey of SNP genotyping laboratories Päivi Lahermo et al. · Human Mutation | 19 Jun 2006 | 21 |
| 30 | Comprehensive Arrayed Primer Extension Array for the Detection of 59 Sequence Variants in 15 Conditions Prevalent Among the (Ashkenazi) Jewish Population Iris Schrijver, Maigi Külm, Phyllis Gardner et al. · Journal of Molecular Diagnostics | 23 Mar 2007 | 21 |
| 31 | Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia Rita Teek, Katrin Kruustük, Riina Žordania et al. · International Journal of Pediatric Otorhinolaryngology | 20 Jun 2010 | 20 |
| 32 | Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene Lorraine N. Clark et al. · Movement Disorders | 5 Apr 2007 | 19 |
| 33 | Arrayed Primer Extension Resequencing of Mutations in the TP53 Tumor Suppressor Gene: Comparison with Denaturing HPLC and Direct Sequencing Florence Le Calvez‐Kelm, Aune Ahman, Neeme Tõnisson et al. · Clinical Chemistry | 23 Jun 2005 | 18 |
| 34 | SNiPORK – A Microarray of SNPs in Candidate Genes Potentially Associated with Pork Yield and Quality – Development and Validation in Commercial Breeds Stanisław Kamiński, Hela Help, P. Brym et al. · Animal Biotechnology | 18 Jan 2008 | 17 |
| 35 | Towards an integrated approach to study SNPs and expression of candidate genes associated with milk protein biosynthesis Stanisław Kamiński, Tadeusz Malewski, Aune Ahman et al. · Russian Journal of Genetics | Apr 2008 | 17 |
| 36 | Ace I/D polymorphism is associated with habitual physical activity in pubertal boys Jarek Mäestu, Evelin Lätt, Triin Rääsk et al. · The Journal of Physiological Sciences | 2 Aug 2013 | 14 |
| 37 | Analysis of NADP+-dependent isocitrate dehydrogenase-1/2 gene mutations in pediatric brain tumors: report of a secondary anaplastic astrocytoma carrying the IDH1 mutation Samantha Mascelli, Alessandro Raso, Roberto Biassoni et al. · Journal of Neuro-Oncology | 21 Jul 2012 | 13 |
| 38 | Screening 52 single nucleotide polymorphisms for extreme value of glycolytic potential and drip loss in pigs Stanisław Kamiński, M. Koćwin‐Podsiadła, H. Sieczkowska et al. · Journal of Animal Breeding and Genetics | 13 Nov 2009 | 11 |
| 39 | Out-of-hospital resuscitation in Estonia: a bystander-witnessed sudden cardiac arrest Aleksander Sipria, Vassili Novak, Aire Veber et al. · European Journal of Emergency Medicine | 21 Dec 2005 | 11 |
| 40 | Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss Rita Teek, Eneli Oitmaa, Katrin Kruustük et al. · International Journal of Pediatric Otorhinolaryngology | 23 Nov 2008 | 11 |
| 41 | The Prevalence and Molecular Landscape of Lynch Syndrome in the Affected and General Population Laura Roht, Piret Laidre, Mikk Tooming et al. · Cancers | 18 Jul 2023 | 10 |
| 42 | Classical galactosemia in Estonia: selective neonatal screening, incidence, and genotype/phenotype data of diagnosed patients Katrin Õunap, Kairit Joost, Triinu Temberg et al. · Journal of Inherited Metabolic Disease | 11 Feb 2010 | 10 |
| 43 | ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia Christos Shammas, Thessalia Papasavva, Xenia Felekis et al. · Clinical Chemistry and Laboratory Medicine (CCLM) | 13 Aug 2010 | 8 |
| 44 | A very early diagnosis of Alstrӧm syndrome by next generation sequencing Leonardo Gatticchi, Ján Miertuš, Paolo Enrico Maltese et al. · BMC Medical Genetics | Sep 2020 | 7 |
| 45 | Leber Congenital Amaurosis: First Genotyped Hungarian Patients and Report of 2 Novel Mutations in the CRB1 and CEP290 Genes Rita Vámos, Maigi Külm, Viktória Szabó et al. · European Journal of Ophthalmology | 7 Feb 2015 | 6 |
| 46 | Additive effects of 19 porcine SNPs on growth rate, meat content and selection index Stanisław Kamiński, Hela Help, Tomasz Suchocki et al. · Journal of Applied Genetics | Sep 2009 | 6 |
| 47 | Arrayed primer extension on in situ synthesized 5′ → 3′ oligonucleotides in microchannels Janne Pullat, Wlad Kusnezow, Kaie Jaakson et al. · New Biotechnology | 15 Aug 2008 | 6 |
| 48 | Lynch syndrome mutations shared by the Baltic States and Poland Dagmara Dymerska et al. · Clinical Genetics | 5 Sep 2013 | 5 |
| 49 | A hybrid approach to device integration on a genetic analysis platform Des Brennan, Dorothée Jary, Ants Kurg et al. · Measurement Science and Technology | 14 Sep 2012 | 5 |
| 50 | Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia Pablo Serrano‐Fernández, Dagmara Dymerska, Grzegorz Kurzawski et al. · Gastroenterology Research and Practice | 2015 | 5 |
Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.