Center of Excellence of the European Union
 
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Recent publications

Articles

1.   Schad E, Kalmar L and Tompa P (2013) [23460204]
  Exon-phase symmetry and intrinsic structural disorder promote modular evolution in the human genome.
  Nucleic Acids Res notSet,
2.   Meggyesi N, Kalmár L, Fekete S, Masszi T, Tordai A and Andrikovics H (2012) [22038725]
  Characterization of ABL exon 7 deletion by molecular genetic and bioinformatic methods reveals no association with imatinib resistance in chronic myeloid leukemia.
  Med Oncol 29, 2136-42
3.   Kalmar L, Acs V, Silhavy D and Tompa P (2012) [22971338]
  Long-range interactions in nonsense-mediated mRNA decay are mediated by intrinsically disordered protein regions.
  J Mol Biol 424, 125-31
4.   Kalmar L, Homola D, Varga G and Tompa P (2012) [22634174]
  Structural disorder in proteins brings order to crystal growth in biomineralization.
  Bone 51, 528-34
5.   Hazy E, Bokor M, Kalmar L, Gelencser A, Kamasa P, Han KH, Tompa K and Tompa P (2011) [22067166]
  Distinct Hydration Properties of Wild-Type and Familial Point Mutant A53T of α-Synuclein Associated with Parkinsons Disease.
  Biophys J 101, 2260-6
6.   Hegyi H, Kalmar L, Horvath T and Tompa P (2011) [20972208]
  Verification of alternative splicing variants based on domain integrity, truncation length and intrinsic protein disorder.
  Nucleic Acids Res 39, 1208-19
7.   Kovacs E, Tompa P, Liliom K and Kalmar L (2010) [20212158]
  Dual coding in alternative reading frames correlates with intrinsic protein disorder.
  P Natl Acad Sci Usa 107, 5429-34
8.   Tompa P and Kalmar L (2010) [20816987]
  Power law distribution defines structural disorder as a structural element directly linked with function.
  J Mol Biol 403, 346-50
9.   Burra PV, Kalmar L and Tompa P (2010) [20711457]
  Reduction in structural disorder and functional complexity in the thermal adaptation of prokaryotes.
  PLoS ONE 5, e12069
10.   Vili N, Horvath MB, Kovacs S, Jozef C, Hornung E and Kalmar L (2009) [-100061774]
  Alternative sampling methods in avian genetic studies: sexing, microsatellites based individual identification and mtDNA analyses of eastern imperial eagles (Aquila heliaca)
  Magy Allatorvosok 131, 426-435
11.   Tusnády GE, Kalmár L and Simon I (2008) [17921502]
  TOPDB: topology data bank of transmembrane proteins.
  Nucleic Acids Res 36, D234-9
12.   Tusnády GE, Kalmár L, Hegyi H, Tompa P and Simon I (2008) [18434342]
  TOPDOM: database of domains and motifs with conservative location in transmembrane proteins.
  Bioinformatics 24, 1469-70
13.   Egyed B, Füredi S, Angyal M, Balogh I, Kalmar L and Padar Z (2006) [16143479]
  Analysis of the population heterogeneity in Hungary using fifteen forensically informative STR markers.
  Forensic Sci Int 158, 244-9
14.   Horvath MB, Martinez-Cruz B, Negro JJ, Kalmár L and Godoy JA (2005) [-142812609]
  An overlooked DNA source for non-invasive genetic analysis in birds
  J Avian Biol 36, 84-88
15.   Szilvási A, Andrikovics H, Kalmár L, Bors A and Tordai A (2005) [15982647]
  Asymmetric PCR increases efficiency of melting peak analysis on the LightCycler.
  Clin Biochem 38, 727-30
16.   Kalmar L, Hegedus T, Farkas H, Nagy M and Tordai A (2005) [15580551]
  Haedb: a novel interactive, locus-specific mutation database for the C1 inhibitor gene
  Hum Mutat 25, 1-5
17.   Bors A, Andrikovics H, Kalmár L, Erdei N, Galambos S, Losonczi A, Füredi S, Balogh I, Szalai C and Tordai A (2004) [15547683]
  Frequencies of two common mutations (c.35delG and c.167delT) of the connexin 26 gene in different populations of Hungary.
  Int J Mol Med 14, 1105-8
18.   Agostoni A, Aygören-Pürsün E, Binkley KE, Blanch A, Bork K, Bouillet L, Bucher C, Castaldo AJ, Cicardi M, Davis AE, De Carolis C, Drouet C, Duponchel C, Farkas H, Fáy K, Fekete B, Fischer B, Fontana L, Füst G, Giacomelli R, Gröner A, Hack CE, Harmat G, Jakenfelds J, Juers M, Kalmár L, Kaposi PN, Karádi I, Kitzinger A, Kollár T, Kreuz W, Lakatos P, Longhurst HJ, Lopez-Trascasa M, Martinez-Saguer I, Monnier N, Nagy I, Németh E, Nielsen EW, Nuijens JH, O\\\'grady C, Pappalardo E, Penna V, Perricone C, Perricone R, Rauch U, Roche O, Rusicke E, Späth PJ, Szendei G, Takács E, Tordai A, Truedsson L, Varga L, Visy B, Williams K, Zanichelli A and Zingale L (2004) [15356535]
  Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.
  J Allergy Clin Immun 114, S51-131
19.   Morar B, Gresham D, Angelicheva D, Tournev I, Gooding R, Guergueltcheva V, Schmidt C, Abicht A, Lochmuller H, Tordai A, Kalmar L, Nagy M, Karcagi V, Jeanpierre M, Herczegfalvi A, Beeson D, Venkataraman V, Warwick Carter K, Reeve J, de Pablo R, Kucinskas V and Kalaydjieva L (2004) [15322984]
  Mutation history of the roma/gypsies.
  Am J Hum Genet 75, 596-609
20.   Kalmár L, Bors A, Farkas H, Vas S, Fandl B, Varga L, Füst G and Tordai A (2003) [14635117]
  Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema.
  Hum Mutat 22, 498
21.   Farkas H, Visy B, Fekete B, Karádi I, Kovács JB, Kovács IB, Kalmár L, Tordai A and Varga L (2002) [12385467]
  Association of celiac disease and hereditary angioneurotic edema.
  Am J Gastroenterol 97, 2682-3
22.   Hunter M, Heyer E, Austerlitz F, Angelicheva D, Nedkova V, Briones P, Gata A, de Pablo R, László A, Bosshard N, Gitzelmann R, Tordai A, Kalmar L, Szalai C, Balogh I, Lupu C, Corches A, Popa G, Perez-Lezaun A and Kalaydjieva LV (2002) [11978884]
  The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across Europe.
  Pediatr Res 51, 602-6
23.   Andrikovics H, Kalmár L, Bors A, Fandl B, Petri I, Kalász L and Tordai A (2001) [11358395]
  Genotype screening for hereditary hemochromatosis among voluntary blood donors in Hungary.
  Blood Cell Mol Dis 27, 334-41
24.   Andrikovics H, Klein I, Kalmár L, Bors A, Jermendy G, Petri I, Kalász L, Váradi A and Tordai A (1999) [10586619]
  [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis]
  Orv Hetil 140, 2517-22
25.   Tordai A, Andrikovics H, Kalmár L, Rajczy K, Pénzes M, Sarkadi B, Klein I and Váradi A (1998) [9783719]
  High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.
  J Med Genet 35, 878-9