• 2107 Citations
  • 21 h-Index
1960 …2009

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Article
2009

Elements of morphology: Standard terminology for the nose and philtrum

Hennekam, R. C. M., Cormier-Daire, V., Hall, J. G., Méhes, K., Patton, M. & Stevenson, R. E., Jan 1 2009, In : American Journal of Medical Genetics, Part A. 149, 1, p. 61-76 16 p.

Research output: Contribution to journalArticle

45 Citations (Scopus)

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency

Komlósi, K., Magyari, L., Talián, G. C., Nemes, É., Káposzta, R., Mogyorósy, G., Méhes, K. & Melegh, B., Dec 2009, In : Journal of inherited metabolic disease. 32, SUPPL. 1, p. S15-S19

Research output: Contribution to journalArticle

7 Citations (Scopus)
2006

A fenotípus pontos leírása: A klinikus hozzájárulása a genotípus-fenotípus összefüggések tisztázásához

Translated title of the contribution: Accurate description of the phenotype: The clinician's contribution to clarification of genotype-phenotype correlationsMéhes, K. & Kosztolányi, G., Jun 11 2006, In : Orvosi hetilap. 147, 23, p. 1059-1061 3 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Excess of malignancies in grandparents of children with malformations? Short Communication

Hadzsiev, K., Tárnok, A., Kosztolányi, G. & Méhes, K., Jul 21 2006, In : Acta biologica Hungarica. 57, 1, p. 137-140 4 p.

Research output: Contribution to journalArticle

2004

Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

Hanks, S., Coleman, K., Reid, S., Plaja, A., Firth, H., FitzPatrick, D., Kidd, A., Méhes, K., Nash, R., Robin, N., Shannon, N., Tolmie, J., Swansbury, J., Irrthum, A., Douglas, J. & Rahman, N., Nov 1 2004, In : Nature genetics. 36, 11, p. 1159-1161 3 p.

Research output: Contribution to journalArticle

410 Citations (Scopus)
27 Citations (Scopus)
2003

Association of Wilms tumor with spinal dysraphism

Méhes, K., Weisenbach, J. & Kajtár, P., Jan 1 2003, In : Pediatric hematology and oncology. 20, 3, p. 261-264 4 p.

Research output: Contribution to journalArticle

10 Citations (Scopus)
9 Citations (Scopus)

Search for factor V Arg306 Cambridge and Hong Kong mutations in mixed Hungarian population samples

Komlósi, K., Havasi, V., Bene, J., Ghosh, M., Szolnoki, Z., Melegh, G., Nagy, Á., Stankovics, J., Császár, A., Papp, E., Gasztonyi, B., Tóth, K., Mózsik, G., Romics, L., Ten Cate, H., Smits, P., Méhes, K., Kosztolányi, G. & Melegh, B., Dec 17 2003, In : Acta Haematologica. 110, 4, p. 220-222 3 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Ulnar/fibular ray defect and brachydactyly in a family: A possible new autosomal dominant syndrome

Morava, É., Czakó, M., Kárteszi, J., Cser, B., Weissbecker, K. & Méhes, K., Jul 2003, In : Clinical Dysmorphology. 12, 3, p. 161-165 5 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)
2002

Association of nonsyndromic Wilms tumor with premature centromere division (PCD)

Méhes, K., Kajtár, P. & Kosztolányi, G., Oct 1 2002, In : American journal of medical genetics. 112, 2, p. 215-216 2 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)

Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia

Morava, É., Kárteszi, J., Weisenbach, J., Caliebe, A., Mundlos, S. & Méhes, K., Dec 31 2002, In : European Journal of Pediatrics. 161, 11, p. 619-622 4 p.

Research output: Contribution to journalArticle

22 Citations (Scopus)

Epithelial Ca2+ channel (ECAC1) in autosomal dominant idiopathic hypercalciuria

Müller, D., Hoenderop, J. G. J., Vennekens, R., Eggert, P., Harangi, F., Méhes, K., Garcia-Nieto, V., Claverie-Martin, F., Van Os, C. H., Nilius, B. & Bindels, R. J. M., Sep 1 2002, In : Nephrology Dialysis Transplantation. 17, 9, p. 1614-1620 7 p.

Research output: Contribution to journalArticle

41 Citations (Scopus)

Gastrointestinal malformations, associated congenital abnormalities, and intrauterine growth

Tárnok, A. & Méhes, K., Jun 8 2002, In : Journal of pediatric gastroenterology and nutrition. 34, 4, p. 406-409 4 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)
2001
13 Citations (Scopus)
2000

A gyógyítás tanítása.

Translated title of the contribution: The teaching of the healing artMéhes, K., Aug 6 2000, In : Orvosi hetilap. 141, 32, p. 1781-1784 4 p.

Research output: Contribution to journalArticle

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation

Kotzot, D., Lurie, I. W., Méhes, K., Werder, E. & Schinzel, A., Oct 19 2000, In : Clinical Genetics. 58, 3, p. 177-180 4 p.

Research output: Contribution to journalArticle

16 Citations (Scopus)
1999

Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy

Melegh, B., Seress, L., Bedekovics, T., Kispál, G., Sümegi, B., Trombitás, K. & Méhes, K., Sep 22 1999, In : Journal of inherited metabolic disease. 22, 7, p. 827-838 12 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)

No chromosomal instability in offspring of survivors of childhood malignancy

Bajnóczky, K., Khezri, S., Kajtár, P. Á., Szücs, R., Kosztolányi, G. & Méhes, K. Á., Feb 1 1999, In : Cancer Genetics and Cytogenetics. 109, 1, p. 79-80 2 p.

Research output: Contribution to journalArticle

8 Citations (Scopus)

No latent chromosome damage in oxygen-exposed premature neonates

Méhes, K., Bajnóczky, K., Adamovich, K., Khezri, S. & Kosztolányi, G., Feb 8 1999, In : Journal of Human Genetics. 44, 1, p. 40-42 3 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian population

Gyürüs, P., Molnár, J., Melegh, B., Tóth, G., Morava, É., Kosztolányi, G. & Méhes, K., Nov 26 1999, In : American journal of medical genetics. 87, 3, p. 245-250 6 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)
1998

A mentális retardatio genetikai kivizsgálása.

Translated title of the contribution: Genetic evaluation of mental retardationMéhes, K. & Kosztolányi, G., Feb 15 1998, In : Orvosi hetilap. 139, 7, p. 339-346 8 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Excess of mild errors of morphogenesis in childhood lymphoblastic leukemia

Méhes, K., Kajtár, P., Sándor, G., Scheel-Walter, M. & Niethammer, D., Jan 6 1998, In : American journal of medical genetics. 75, 1, p. 22-27 6 p.

Research output: Contribution to journalArticle

20 Citations (Scopus)

Gyermekkori malignus betegségböl gyógyultak utódainak vizsgálata.

Translated title of the contribution: Study of offsprings of survivors of childhood malignant diseasesMéhes, K., Szücs, R., Khezri, S., Kajtár, P., Bajnóczky, K. & Kosztolányi, G., Dec 6 1998, In : Orvosi hetilap. 139, 49, p. 2947-2949 3 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Homoplastic A12,753G mitochondrial DNA mutation in a Hungarian family

Kis, A., Matolcsy, A., Vécsei, L., Kosztolányi, G., Méhes, K. & Melegh, B., Dec 1 1998, In : Acta biologica Hungarica. 49, 1, p. 119-124 6 p.

Research output: Contribution to journalArticle

Isolated hypospadias is not associated with signs of midline closure defects

Méhes, K., Jan 13 1998, In : American journal of medical genetics. 75, 2, p. 190-192 3 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)
1997

Allásfoglalás a só fluordúsításának a fogszuvasodás megelözése céljából történö bevezetéséröl.

Translated title of the contribution: Taking position on the introduction of fluoridation for the prevention of dental cariesMéhes, K., Dec 1997, In : Fogorvosi szemle. 90, 12, p. 359-360 2 p.

Research output: Contribution to journalArticle

51 Citations (Scopus)
1996

Familial association of supernumerary nipple with renal cancer

Méhes, K., Feb 1996, In : Cancer Genetics and Cytogenetics. 86, 2, p. 129-130 2 p.

Research output: Contribution to journalArticle

21 Citations (Scopus)

Multiple mitochondrial DNA deletions and persistent hyperthermia in a patient with Brachmann-De Lange phenotype

Melegh, B., Bock, I., Gati, I. & Mehes, K., Oct 19 1996, In : American journal of medical genetics. 65, 1, p. 82-88 7 p.

Research output: Contribution to journalArticle

10 Citations (Scopus)

Objective analysis of centromere separation

Méhes, G., Tárnok, A., Pajor, L. & Méhes, K., Mar 1996, In : Human genetics. 97, 3, p. 365-366 2 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)

Physicians' attitudes regarding Down syndrome

Hermann, R. & Méhes, K., Jan 1 1996, In : Journal of Child Neurology. 11, 1, p. 66-70 5 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Plasma amino acid concentrations in healthy, full-term infants fed hydrolysate infant formula

Decsi, T., Veitl, V., Szász, M., Pintér, Z. & Méhes, K., Jan 12 1996, In : Journal of pediatric gastroenterology and nutrition. 22, 1, p. 62-67 6 p.

Research output: Contribution to journalArticle

16 Citations (Scopus)
1995

Mitokondriális DNS deléció herediter cardio-encephalo-myopathiában.

Translated title of the contribution: Mitochondrial DNA deletion in hereditary cardio-encephalo-myopathyMelegh, B., Seress, L., Sümegi, B., Trombitás, K., Bock, I., Kispál, G., Oláh, E. & Méhes, K., Jun 11 1995, In : Orvosi hetilap. 136, 24, p. 1275-1279 5 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Premature centromere division: A possible manifestation of chromosome instability

Mehes, K. & Buhler, E. M., Mar 13 1995, In : American journal of medical genetics. 56, 1, p. 76-79 4 p.

Research output: Contribution to journalArticle

33 Citations (Scopus)
7 Citations (Scopus)

Uniparental disomy 7 in silver - russell syndrome and primordial growth retardation

Kotzot, D., Schmitt, S., Bernasconi, F., Robinson, W. P., Lurie, I. W., Ilyina, H., Méhes, K., Hamel, B. C. J., Otten, B. J., Hergersberg, M., Werder, E., Schoenle, E. & Schinzel, A., Apr 1 1995, In : Human molecular genetics. 4, 4, p. 583-587 5 p.

Research output: Contribution to journalArticle

235 Citations (Scopus)
1994

Bilateral Coats retinopathy associated with aplastic anaemia and mild dyskeratotic signs

Kajtar, P. & Mehes, K., Jan 1 1994, In : American journal of medical genetics. 49, 4, p. 374-377 4 p.

Research output: Contribution to journalArticle

41 Citations (Scopus)
1993
6 Citations (Scopus)
4 Citations (Scopus)

Family investigations in idiopathic hypercalciuria

Harangi, F. & Méhes, K., Jan 1 1993, In : European Journal of Pediatrics. 152, 1, p. 64-68 5 p.

Research output: Contribution to journalArticle

34 Citations (Scopus)

No effect of vanadate on the centromere separation sequence.

Tárnok, A., Méhes, K. & Kosztolányi, G., 1993, In : Acta biologica Hungarica. 44, 2-3, p. 297-301 5 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)
1992

A possible mosaic form of delayed centromere separation and aneuploidy

Méhes, K. & Kosztolányi, G., Feb 1 1992, In : Human genetics. 88, 4, p. 477-478 2 p.

Research output: Contribution to journalArticle

8 Citations (Scopus)
1991

Balanced chromosome rearrangements and abnormal phenotype.

Kosztolányi, G., Bajnóczky, K. & Méhes, K., 1991, In : Acta paediatrica Hungarica. 31, 4, p. 397-402 6 p.

Research output: Contribution to journalArticle

Dysmorphology in Children with Congenital Metabolic Disorders

Méhes, K., Aug 1991, In : Pediatrics International. 33, 4, p. 440-442 3 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

Inherited ring chromosomes: an analysis of published cases

Kosztolányi, G., Méhes, K. & Hook, E. B., Jul 1 1991, In : Human genetics. 87, 3, p. 320-324 5 p.

Research output: Contribution to journalArticle

60 Citations (Scopus)

Late separating D/D fusions in subjects with 'balanced' translocation

Mehes, K., Bajnoczky, K., Buhler, E. M. & Kosztolanyi, G., Jul 19 1991, In : Annales de Genetique. 34, 1, p. 19-21 3 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)
1990

Minor morphological aberrations in children with isolated urinary tract malformations

Méhes, K. & Pintér, A., Mar 1 1990, In : European Journal of Pediatrics. 149, 6, p. 399-402 4 p.

Research output: Contribution to journalArticle

20 Citations (Scopus)

MORPHOGENETISCHE VARIANTEN BEI ELTERN VON KINDERN MIT REZESSIVEN MISSBILDUNGSSYNDROMEN

Translated title of the contribution: Morphogenetic variants in parents of children with recessive multiple malformation syndromesMehes, K., Jan 1 1990, In : Kinderarztliche Praxis. 58, 3, p. 125-130 6 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)