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Papers authored by Hilgert N

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Function and expression pattern of nonsyndromic deafness genes.

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Hilgert N, Smith RJ, and Van Camp G

Current molecular medicine 9(5):546-64, 2009 Jul - Who cited this? | PubMed ID: 19601806 | Fulltext

Milk acidification by Lactococcus lactis is improved by decreasing the level of dissolved oxygen rather than decreasing redox potential in the milk prior to inoculation.

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Jeanson S, Hilgert N, Coquillard MO, Seukpanya C, Faiveley M, Neveu P, Abraham C, Georgescu V, Fourcassié P, and Beuvier E

International journal of food microbiology 131(1):75-81, 2009 Apr 30 - Who cited this? | PubMed ID: 18986723 | Fulltext

Novel human pathological mutations. Gene symbol: GPR98. Disease: Usher syndrome 2C.

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Hilgert N

Human genetics 125(3):342, 2009 Apr - Who cited this? | PubMed ID: 19320012 | Fulltext

A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family.

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Hilgert N, Kahrizi K, Dieltjens N, Bazazzadegan N, Najmabadi H, Smith RJ, and Van Camp G

Journal of medical genetics 46(4):272-6, 2009 Apr - Who cited this? | PubMed ID: 19357116 | Fulltext

Are MYO1C and MYO1F associated with hearing loss?.

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Zadro C, Alemanno MS, Bellacchio E, Ficarella R, Donaudy F, Melchionda S, Zelante L, Rabionet R, Hilgert N, Estivill X, Van Camp G, Gasparini P, and Carella M

Biochimica et biophysica acta 1792(1):27-32, 2009 Jan - Who cited this? | PubMed ID: 19027848 | Fulltext

Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?.

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Hilgert N, Smith RJ, and Van Camp G

Mutation research 681(2-3):189-96, 2009 - Who cited this? | PubMed ID: 18804553 | Fulltext

Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment.

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Hilgert N, Monahan K, Kurima K, Li C, Friedman RA, Griffith AJ, and Van Camp G

Journal of human genetics 54(3):188-90, 2009 - Who cited this? | PubMed ID: 19180119 | Fulltext

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.

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Hilgert N, Huentelman MJ, Thorburn AQ, Fransen E, Dieltjens N, Mueller-Malesinska M, Pollak A, Skorka A, Waligora J, Ploski R, Castorina P, Primignani P, Ambrosetti U, Murgia A, Orzan E, Pandya A,

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European journal of human genetics : EJHG, 2008 Nov 5 - Who cited this? | PubMed ID: 18985073 | Fulltext

Gene symbol: TMC1. Disease: Deafness.

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Hilgert N

Human genetics 124(3):305, 2008 Oct - Who cited this? | PubMed ID: 18846636 | Fulltext

Gene symbol: TMC1. Disease: Hearing loss.

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Hilgert N

Human genetics 124(3):305, 2008 Oct - Who cited this? | PubMed ID: 18846637 | Fulltext

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.

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Hilgert N, Alasti F, Dieltjens N, Pawlik B, Wollnik B, Uyguner O, Delmaghani S, Weil D, Petit C, Danis E, Yang T, Pandelia E, Petersen M, Goossens D, Favero J, Sanati M,

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Clinical genetics, 2008 Jun 26 - Who cited this? | PubMed ID: 18616530 | Fulltext

A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss.

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Hilgert N, Topsakal V, van Dinther J, Offeciers E, Van de Heyning P, and Van Camp G

European journal of human genetics : EJHG 16(5):593-602, 2008 May - Who cited this? | PubMed ID: 18212818 | Fulltext

A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9.

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Bel Hadj Ali I, Thys M, Beltaief N, Schrauwen I, Hilgert N, Vanderstraeten K, Dieltjens N, Mnif E, Hachicha S, Besbes G, Ben Arab S, and Van Camp G

Human genetics 123(3):267, 2008 Apr - Who cited this? | PubMed ID: 18224337 | Fulltext

Reproductive medicine in northwest Argentina: traditional and institutional systems.

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Hilgert NI and Gil GE

Journal of ethnobiology and ethnomedicine 3:19, 2007 - Who cited this? | PubMed ID: 17475013 | Fulltext

A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene.

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Van Camp G, Snoeckx RL, Hilgert N, van den Ende J, Fukuoka H, Wagatsuma M, Suzuki H, Smets RM, Vanhoenacker F, Declau F, Van de Heyning P, and Usami S

American journal of human genetics 79(3):449-57, 2006 Sep - Who cited this? | PubMed ID: 16909383 | Fulltext

GJB2 mutations and degree of hearing loss: a multicenter study.

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Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, Wiszniewski W,

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American journal of human genetics 77(6):945-57, 2005 Dec - Who cited this? | PubMed ID: 16380907 | Fulltext

Modeling the effects of assimilable nitrogen and temperature on fermentation kinetics in enological conditions.

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Malherbe S, Fromion V, Hilgert N, and Sablayrolles JM

Biotechnology and bioengineering 86(3):261-72, 2004 May 5 - Who cited this? | PubMed ID: 15083506 | Fulltext

Plants used in home medicine in the Zenta River basin, Northwest Argentina.

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Hilgert NI

Journal of ethnopharmacology 76(1):11-34, 2001 Jun - Who cited this? | PubMed ID: 11378277 | Fulltext

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