-
1
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
Andrews R.M., Kubacka I., Chinnery P.F., Lightowlers R.N., Turnbull D.M., Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet. 1999, 23:147.
-
(1999)
Nat Genet.
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Turnbull, D.M.5
Howell, N.6
-
2
-
-
0030849125
-
Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study
-
Bai U., Seidman M.D., Hinojosa R., Quirk W.S. Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study. Am J Otol. 1997, 18:449-453.
-
(1997)
Am J Otol.
, vol.18
, pp. 449-453
-
-
Bai, U.1
Seidman, M.D.2
Hinojosa, R.3
Quirk, W.S.4
-
3
-
-
48749125930
-
Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective, a European population-based multicenter study
-
Bonaconsa A., Mazzoli M., Espeso A., Verbruggen K., Huyghe J., Huygen P.L.M., Kunst S., Manninen M., Diaz-Lacava A., Steffens M., Wienker T.F., Pyyko I., Cremers C., Kremer H., Dhooge I., Stephens D., Orzan E., Pfister M., Bille M., Parving A., Sorri M., Van De Heyning P., Van Camp G. Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective, a European population-based multicenter study. J Assoc for Res Otolaryngol. 2008, 9:264-276.
-
(2008)
J Assoc for Res Otolaryngol.
, vol.9
, pp. 264-276
-
-
Bonaconsa, A.1
Mazzoli, M.2
Espeso, A.3
Verbruggen, K.4
Huyghe, J.5
Huygen, P.L.M.6
Kunst, S.7
Manninen, M.8
Diaz-Lacava, A.9
Steffens, M.10
Wienker, T.F.11
Pyyko, I.12
Cremers, C.13
Kremer, H.14
Dhooge, I.15
Stephens, D.16
Orzan, E.17
Pfister, M.18
Bille, M.19
Parving, A.20
Sorri, M.21
Van De Heyning, P.22
Van Camp, G.23
more..
-
4
-
-
13044279515
-
Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications
-
Casano R., Johnson D.F., Bykhovskaya Y., Torricelli F., Bigozzi M., Fischel-Ghodsian N. Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications. Am J Otolaryngol. 1999, 20:151-156.
-
(1999)
Am J Otolaryngol.
, vol.20
, pp. 151-156
-
-
Casano, R.1
Johnson, D.F.2
Bykhovskaya, Y.3
Torricelli, F.4
Bigozzi, M.5
Fischel-Ghodsian, N.6
-
5
-
-
1642267429
-
Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis
-
Dai P., Yang W., Jiang S., Gu R., Yuan H., Han D., Guo W., Cao J. Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis. Acta Otolaryngol. 2004, 124:130-136.
-
(2004)
Acta Otolaryngol.
, vol.124
, pp. 130-136
-
-
Dai, P.1
Yang, W.2
Jiang, S.3
Gu, R.4
Yuan, H.5
Han, D.6
Guo, W.7
Cao, J.8
-
6
-
-
1642426851
-
Prevalence of hearing impairment
-
Whurr Publishers Ltd., Londen, A. Davis.
-
Davis A. Prevalence of hearing impairment. Hearing in Adults 1994, 43-321. Whurr Publishers Ltd., Londen, A. Davis.
-
(1994)
Hearing in Adults
, pp. 43-321
-
-
Davis, A.1
-
7
-
-
77953026831
-
Heritability of audiometric shape parameters and familial aggregation of presbycusis in an elderly Flemish population
-
Demeester K., van Wieringen A., Hendrickx J.J., Topsakal V., Huyghe J., Fransen E., Van Laer L., Van Camp G., Van de Heyning P. Heritability of audiometric shape parameters and familial aggregation of presbycusis in an elderly Flemish population. Hear Res. 2010, 265:1-10.
-
(2010)
Hear Res.
, vol.265
, pp. 1-10
-
-
Demeester, K.1
van Wieringen, A.2
Hendrickx, J.J.3
Topsakal, V.4
Huyghe, J.5
Fransen, E.6
Van Laer, L.7
Van Camp, G.8
Van de Heyning, P.9
-
8
-
-
0033917385
-
Mutations in mtDNA, are we scraping the bottom of the barrel?
-
DiMauro S., Andreu A.L. Mutations in mtDNA, are we scraping the bottom of the barrel?. Brain Pathol. 2000, 10:431-441.
-
(2000)
Brain Pathol.
, vol.10
, pp. 431-441
-
-
DiMauro, S.1
Andreu, A.L.2
-
9
-
-
0030745117
-
Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations
-
Fischel-Ghodsian N., Bykhovskaya Y., Taylor K., Kahen T., Cantor R., Ehrenman K., Smith R., Keithley E. Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations. Hear Res. 1997, 110:147-154.
-
(1997)
Hear Res.
, vol.110
, pp. 147-154
-
-
Fischel-Ghodsian, N.1
Bykhovskaya, Y.2
Taylor, K.3
Kahen, T.4
Cantor, R.5
Ehrenman, K.6
Smith, R.7
Keithley, E.8
-
10
-
-
1842507428
-
A novel Z-score-based method to analyze candidate genes for age-related hearing impairment
-
Fransen E., Van Laer L., Lemkens N., Caethoven G., Flothmann K., Govaerts P., Van de Heyning P., Van Camp G. A novel Z-score-based method to analyze candidate genes for age-related hearing impairment. Ear Hear. 2004, 25:133-141.
-
(2004)
Ear Hear.
, vol.25
, pp. 133-141
-
-
Fransen, E.1
Van Laer, L.2
Lemkens, N.3
Caethoven, G.4
Flothmann, K.5
Govaerts, P.6
Van de Heyning, P.7
Van Camp, G.8
-
11
-
-
58949089599
-
GRM7 variants confer susceptibility to age-related hearing impairment
-
Friedman R.A., Van Laer L., Huentelman M.J., Sheth S.S., Van Eyken E., Corneveaux J.J., Tembe W.D., Halperin R.F., Thorburn A.Q., Thys S., Bonneux S., Fransen E., Huyghe J., Pyykkö I., Cremers C.W., Kremer H., Dhooge I., Stephens D., Orzan E., Pfister M., Bille M., Parving A., Sorri M., Van de Heyning P.H., Makmura L., Ohmen J.D., Linthicum F.H., Fayad J.N., Pearson J.V., Craig D.W., Stephan D.A., Van Camp G. GRM7 variants confer susceptibility to age-related hearing impairment. Hum Mol Genet. 2009, 18:785-796.
-
(2009)
Hum Mol Genet.
, vol.18
, pp. 785-796
-
-
Friedman, R.A.1
Van Laer, L.2
Huentelman, M.J.3
Sheth, S.S.4
Van Eyken, E.5
Corneveaux, J.J.6
Tembe, W.D.7
Halperin, R.F.8
Thorburn, A.Q.9
Thys, S.10
Bonneux, S.11
Fransen, E.12
Huyghe, J.13
Pyykkö, I.14
Cremers, C.W.15
Kremer, H.16
Dhooge, I.17
Stephens, D.18
Orzan, E.19
Pfister, M.20
Bille, M.21
Parving, A.22
Sorri, M.23
Van de Heyning, P.H.24
Makmura, L.25
Ohmen, J.D.26
Linthicum, F.H.27
Fayad, J.N.28
Pearson, J.V.29
Craig, D.W.30
Stephan, D.A.31
Van Camp, G.32
more..
-
13
-
-
38749145596
-
Shifting paradigm of association studies, value of rare single-nucleotide polymorphisms
-
Gorlov I.P., Gorlova O.Y., Sunyaev S.R., Spitz M.R., Amos C.I. Shifting paradigm of association studies, value of rare single-nucleotide polymorphisms. Am J Hum Genet. 2008, 82:100-112.
-
(2008)
Am J Hum Genet.
, vol.82
, pp. 100-112
-
-
Gorlov, I.P.1
Gorlova, O.Y.2
Sunyaev, S.R.3
Spitz, M.R.4
Amos, C.I.5
-
14
-
-
33646855427
-
Mitochondrial DNA mutations in human disease
-
Greaves L.C., Taylor R.W. Mitochondrial DNA mutations in human disease. Iubmb Life 2006, 58:143-151.
-
(2006)
Iubmb Life
, vol.58
, pp. 143-151
-
-
Greaves, L.C.1
Taylor, R.W.2
-
15
-
-
58349116644
-
Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes
-
Hartmann A., Thieme M., Nanduri L.K., Stempfl T., Moehle C., Kivisild T., Oefner P.J. Validation of microarray-based resequencing of 93 worldwide mitochondrial genomes. Human Mutat. 2009, 30:115-122.
-
(2009)
Human Mutat.
, vol.30
, pp. 115-122
-
-
Hartmann, A.1
Thieme, M.2
Nanduri, L.K.3
Stempfl, T.4
Moehle, C.5
Kivisild, T.6
Oefner, P.J.7
-
16
-
-
0029101232
-
Human aging is associated with stochastic somatic mutations of mitochondrial-DNA
-
Kadenbach B., Munscher C., Frank V., Mullerhocker J., Napiwotzki J. Human aging is associated with stochastic somatic mutations of mitochondrial-DNA. Mutation Res. 1995, 338:161-172.
-
(1995)
Mutation Res.
, vol.338
, pp. 161-172
-
-
Kadenbach, B.1
Munscher, C.2
Frank, V.3
Mullerhocker, J.4
Napiwotzki, J.5
-
17
-
-
0030964943
-
Description and primary results from an audiometric study of male twins
-
Karlsson K.K., Harris J.R., Svartengren M. Description and primary results from an audiometric study of male twins. Ear Hear. 1997, 18:114-120.
-
(1997)
Ear Hear.
, vol.18
, pp. 114-120
-
-
Karlsson, K.K.1
Harris, J.R.2
Svartengren, M.3
-
18
-
-
33244457956
-
The role of selection in the evolution of human mitochondrial genomes
-
Kivisild T., Shen P.D., Wall D.P., Do B., Sung R., Davis K., Passarino G., Underhill P.A., Scharfe C., Torroni A., Scozzari R., Modiano D., Coppa A., de Knijff P., Feldman M., Cavalli-Sforza L.L., Oefner P.J. The role of selection in the evolution of human mitochondrial genomes. Genetics. 2006, 172:373-387.
-
(2006)
Genetics.
, vol.172
, pp. 373-387
-
-
Kivisild, T.1
Shen, P.D.2
Wall, D.P.3
Do, B.4
Sung, R.5
Davis, K.6
Passarino, G.7
Underhill, P.A.8
Scharfe, C.9
Torroni, A.10
Scozzari, R.11
Modiano, D.12
Coppa, A.13
de Knijff, P.14
Feldman, M.15
Cavalli-Sforza, L.L.16
Oefner, P.J.17
-
20
-
-
22344456832
-
Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging
-
Kujoth G.C., Hiona A., Pugh T.D., Someya S., Panzer K., Wohlgemuth S.E., Hofer T., Seo A.Y., Sullivan R., Jobling W.A., Morrow J.D., Van Remmen H., Sedivy J.M., Yamasoba Y., Tanokura T., Weindruch R., Leeuwenburgh C., Prolla T.A. Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science. 2005, 309:481-484.
-
(2005)
Science.
, vol.309
, pp. 481-484
-
-
Kujoth, G.C.1
Hiona, A.2
Pugh, T.D.3
Someya, S.4
Panzer, K.5
Wohlgemuth, S.E.6
Hofer, T.7
Seo, A.Y.8
Sullivan, R.9
Jobling, W.A.10
Morrow, J.D.11
Van Remmen, H.12
Sedivy, J.M.13
Yamasoba, Y.14
Tanokura, T.15
Weindruch, R.16
Leeuwenburgh, C.17
Prolla, T.A.18
-
21
-
-
0043066954
-
Increased variation in mtDNA in patients with familial sensorineural hearing impairment
-
Lehtonen M.S., Moilanen J.S., Majamaa K. Increased variation in mtDNA in patients with familial sensorineural hearing impairment. Hum Genet. 2003, 1133:220-227.
-
(2003)
Hum Genet.
, vol.1133
, pp. 220-227
-
-
Lehtonen, M.S.1
Moilanen, J.S.2
Majamaa, K.3
-
22
-
-
35548963935
-
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
-
Leveque M., Marlin S., Jonard L., Procaccio V., Reynier P., Amati-Bonneau P., Baulande S., Pierron D., Lacombe D., Duriez F., Francannet C., Mom T., Journel H., Catros H., Dourin-Garraud V., Obstoy M.F., Dollfus H., Eliot M.M., Faivre L., Duvillard C., Couderc R., Garabedian E.N., Petit C., Feldmann D., Denoyelle F. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. Eur J Hum Genet. 2007, 15:1145-1155.
-
(2007)
Eur J Hum Genet.
, vol.15
, pp. 1145-1155
-
-
Leveque, M.1
Marlin, S.2
Jonard, L.3
Procaccio, V.4
Reynier, P.5
Amati-Bonneau, P.6
Baulande, S.7
Pierron, D.8
Lacombe, D.9
Duriez, F.10
Francannet, C.11
Mom, T.12
Journel, H.13
Catros, H.14
Dourin-Garraud, V.15
Obstoy, M.F.16
Dollfus, H.17
Eliot, M.M.18
Faivre, L.19
Duvillard, C.20
Couderc, R.21
Garabedian, E.N.22
Petit, C.23
Feldmann, D.24
Denoyelle, F.25
more..
-
23
-
-
50949095168
-
Novel methods for detecting associations with rare variants for common diseases, application to analysis of sequence data
-
Li B., Leal S.M. Novel methods for detecting associations with rare variants for common diseases, application to analysis of sequence data. Am J Hum Genet. 2008, 83:311-321.
-
(2008)
Am J Hum Genet.
, vol.83
, pp. 311-321
-
-
Li, B.1
Leal, S.M.2
-
24
-
-
2442720182
-
The human MitoChip, a high-throughput sequencing microarray for mitochondrial mutation detection
-
Maitra A., Cohen Y., Gillespie S.E.D., Mambo E., Fukushima N., Hoque M.O., Shah N., Goggins M., Califano J., Sidransky D., Chakravarti A. The human MitoChip, a high-throughput sequencing microarray for mitochondrial mutation detection. Genome Res. 2004, 14:812-819.
-
(2004)
Genome Res.
, vol.14
, pp. 812-819
-
-
Maitra, A.1
Cohen, Y.2
Gillespie, S.E.D.3
Mambo, E.4
Fukushima, N.5
Hoque, M.O.6
Shah, N.7
Goggins, M.8
Califano, J.9
Sidransky, D.10
Chakravarti, A.11
-
25
-
-
34548781484
-
Mitochondrial DNA haplogroups and age-related hearing loss
-
Manwaring N., Jones M.M., Wang J.J., Rochtchina E., Howard C., Newall P., Mitchell P., Sue C.M. Mitochondrial DNA haplogroups and age-related hearing loss. Arch Otolaryngol Head Neck Surg. 2007, 133:929-933.
-
(2007)
Arch Otolaryngol Head Neck Surg.
, vol.133
, pp. 929-933
-
-
Manwaring, N.1
Jones, M.M.2
Wang, J.J.3
Rochtchina, E.4
Howard, C.5
Newall, P.6
Mitchell, P.7
Sue, C.M.8
-
26
-
-
66849141801
-
Quantification of the mitochondrial DNA common deletion in presbycusis
-
Markaryan A., Nelson E.G., Hinojosa R. Quantification of the mitochondrial DNA common deletion in presbycusis. Laryngoscope. 2009, 119:1184-1189.
-
(2009)
Laryngoscope.
, vol.119
, pp. 1184-1189
-
-
Markaryan, A.1
Nelson, E.G.2
Hinojosa, R.3
-
28
-
-
67349268943
-
20years of human mtDNA pathologic point mutations, carefully reading the pathogenicity criteria
-
Montoya J., Lopez-Gallardo E., Diez-Sanchez C., Lopez-Perez M.J., Ruiz-Pesini E. 20years of human mtDNA pathologic point mutations, carefully reading the pathogenicity criteria. Biochim Biophys Acta. 2009, 1787:476-483.
-
(2009)
Biochim Biophys Acta.
, vol.1787
, pp. 476-483
-
-
Montoya, J.1
Lopez-Gallardo, E.2
Diez-Sanchez, C.3
Lopez-Perez, M.J.4
Ruiz-Pesini, E.5
-
29
-
-
65149104318
-
The diversity present in 5140 human mitochondrial genomes
-
Pereira L., Freitas F., Fernandes V., Pereira J.B., Costa M.D., Costa S., Maximo V., Macaulay V., Rocha R., Samuels D.C. The diversity present in 5140 human mitochondrial genomes. Am J Hum Genet. 2009, 84:628-640.
-
(2009)
Am J Hum Genet.
, vol.84
, pp. 628-640
-
-
Pereira, L.1
Freitas, F.2
Fernandes, V.3
Pereira, J.B.4
Costa, M.D.5
Costa, S.6
Maximo, V.7
Macaulay, V.8
Rocha, R.9
Samuels, D.C.10
-
31
-
-
57649210205
-
Mitochondrial DNA mutations in disease, aging, and neurodegeneration
-
Reeve A.K., Krishnan K.J., Turnbull D. Mitochondrial DNA mutations in disease, aging, and neurodegeneration. Ann N Y Acad Sci. 2008, 1147:21-29.
-
(2008)
Ann N Y Acad Sci.
, vol.1147
, pp. 21-29
-
-
Reeve, A.K.1
Krishnan, K.J.2
Turnbull, D.3
-
32
-
-
33745273048
-
Comprehensive association testing of common mitochondrial DNA variation in metabolic disease
-
Saxena R., de Bakker P.I.W., Singer K., Mootha V., Burtt N., Hirschhorn J.N., Gaudet D., Isomaa B., Daly M.J., Groop L., Ardlie K.G., Altshuler D. Comprehensive association testing of common mitochondrial DNA variation in metabolic disease. Am J Hum Genet. 2006, 79:54-61.
-
(2006)
Am J Hum Genet.
, vol.79
, pp. 54-61
-
-
Saxena, R.1
de Bakker, P.I.W.2
Singer, K.3
Mootha, V.4
Burtt, N.5
Hirschhorn, J.N.6
Gaudet, D.7
Isomaa, B.8
Daly, M.J.9
Groop, L.10
Ardlie, K.G.11
Altshuler, D.12
-
33
-
-
0029945725
-
Association of mitochondrial DNA deletions and cochlear pathology, a molecular biologic tool
-
Seidman M.D., Bai U., Khan M.J., Murphy M.J., Quirk W.S., Castora F.L., Hinojosa R. Association of mitochondrial DNA deletions and cochlear pathology, a molecular biologic tool. Laryngoscope. 1996, 106:777-783.
-
(1996)
Laryngoscope.
, vol.106
, pp. 777-783
-
-
Seidman, M.D.1
Bai, U.2
Khan, M.J.3
Murphy, M.J.4
Quirk, W.S.5
Castora, F.L.6
Hinojosa, R.7
-
34
-
-
0030730676
-
Mitochondrial DNA deletions associated with aging and presbyacusis
-
Seidman M.D., Bai U., Khan M.J., Quirk W.S. Mitochondrial DNA deletions associated with aging and presbyacusis. Arch Otolaryngol Head Neck Surg. 1997, 123:1039-1045.
-
(1997)
Arch Otolaryngol Head Neck Surg.
, vol.123
, pp. 1039-1045
-
-
Seidman, M.D.1
Bai, U.2
Khan, M.J.3
Quirk, W.S.4
-
35
-
-
0034056134
-
Biologic activity of mitochondrial metabolites on aging and age-related hearing loss
-
Seidman M.D., Khan M.J., Bai U., Shirwany N., Quirk W.S. Biologic activity of mitochondrial metabolites on aging and age-related hearing loss. Am J Otol. 2000, 21:161-167.
-
(2000)
Am J Otol.
, vol.21
, pp. 161-167
-
-
Seidman, M.D.1
Khan, M.J.2
Bai, U.3
Shirwany, N.4
Quirk, W.S.5
-
36
-
-
0036593360
-
Molecular mechanisms of age-related hearing loss
-
Seidman M.D., Ahmad N., Bai U. Molecular mechanisms of age-related hearing loss. Ageing Res Rev. 2002, 1:331-343.
-
(2002)
Ageing Res Rev.
, vol.1
, pp. 331-343
-
-
Seidman, M.D.1
Ahmad, N.2
Bai, U.3
-
37
-
-
0028095263
-
MtDNA and the origin of Caucasians, identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region
-
Torroni A., Lott M.T., Cabell M.F., Chen Y.S., Lavergne L., Wallace D.C. mtDNA and the origin of Caucasians, identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet. 1994, 55:760-776.
-
(1994)
Am J Hum Genet.
, vol.55
, pp. 760-776
-
-
Torroni, A.1
Lott, M.T.2
Cabell, M.F.3
Chen, Y.S.4
Lavergne, L.5
Wallace, D.C.6
-
38
-
-
0030468182
-
Classification of European mtDNAs from an analysis three European populations
-
Torroni A., Huoponen K., Francalacci P., Petrozzi M., Morelli L., Scozzari R., Obinu D., Savontaus M.L., Wallace D.C. Classification of European mtDNAs from an analysis three European populations. Genetics. 1996, 144:1835-1850.
-
(1996)
Genetics.
, vol.144
, pp. 1835-1850
-
-
Torroni, A.1
Huoponen, K.2
Francalacci, P.3
Petrozzi, M.4
Morelli, L.5
Scozzari, R.6
Obinu, D.7
Savontaus, M.L.8
Wallace, D.C.9
-
39
-
-
2642580016
-
Premature ageing in mice expressing defective mitochondrial DNA polymerase
-
Trifunovic A., Wredenberg A., Falkenberg M., Spelbrink J.N., Rovio A.T., Bruder C.E., Bohlooly-Y M., Gidlof S.M., Oldfors A., Wibom R., Tornell J., Jacobs H.T., Larsson N.G. Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature. 2004, 429:417-423.
-
(2004)
Nature.
, vol.429
, pp. 417-423
-
-
Trifunovic, A.1
Wredenberg, A.2
Falkenberg, M.3
Spelbrink, J.N.4
Rovio, A.T.5
Bruder, C.E.6
Bohlooly-Y, M.7
Gidlof, S.M.8
Oldfors, A.9
Wibom, R.10
Tornell, J.11
Jacobs, H.T.12
Larsson, N.G.13
-
41
-
-
33750543175
-
Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients
-
van Eijsden R.G.E., Gerards M., Eijssen L.M.T., Hendrickx A.T.M., Jongbloed R.J.E., Wokke J.H.J., Hintzen R.Q., Rubio-Gozalbo M.E., De Coo I.F.M., Briem E., Tiranti V., Smeets H.J.M. Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients. Genet Med. 2006, 8:620-627.
-
(2006)
Genet Med.
, vol.8
, pp. 620-627
-
-
van Eijsden, R.G.E.1
Gerards, M.2
Eijssen, L.M.T.3
Hendrickx, A.T.M.4
Jongbloed, R.J.E.5
Wokke, J.H.J.6
Hintzen, R.Q.7
Rubio-Gozalbo, M.E.8
De Coo, I.F.M.9
Briem, E.10
Tiranti, V.11
Smeets, H.J.M.12
-
42
-
-
33748999299
-
KCNQ4, a gene for age-related hearing impairment?
-
Van Eyken E., Van Laer L., Fransen E., Topsakal V., Lemkens N., Laureys W., Nelissen N., Vandevelde A., Wienker T., Van De Heyning P., Van Camp G. KCNQ4, a gene for age-related hearing impairment?. Hum Mutat. 2006, 27:1007-1016.
-
(2006)
Hum Mutat.
, vol.27
, pp. 1007-1016
-
-
Van Eyken, E.1
Van Laer, L.2
Fransen, E.3
Topsakal, V.4
Lemkens, N.5
Laureys, W.6
Nelissen, N.7
Vandevelde, A.8
Wienker, T.9
Van De Heyning, P.10
Van Camp, G.11
-
43
-
-
34548827061
-
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment
-
Van Eyken E., Van Camp G., Fransen E., Topsakal V., Hendrickx J.J., Demeester K., Van de Heyning P., Maki-Torkko E., Hannula S., Sorri M., Jensen M., Parving A., Bille M., Baur M., Pfister M., Bonaconsa A., Mazzoli M., Orzan E., Espeso A., Stephens D., Verbruggen K., Huyghe J., Dhooge I., Huygen P., Kremer H., Cremers C.W., Kunst S., Manninen M., Pyykko I., Lacava A., Steffens M., Wienker T.F., Van Laer L. Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment. J Med Genet. 2007, 44:570-578.
-
(2007)
J Med Genet.
, vol.44
, pp. 570-578
-
-
Van Eyken, E.1
Van Camp, G.2
Fransen, E.3
Topsakal, V.4
Hendrickx, J.J.5
Demeester, K.6
Van de Heyning, P.7
Maki-Torkko, E.8
Hannula, S.9
Sorri, M.10
Jensen, M.11
Parving, A.12
Bille, M.13
Baur, M.14
Pfister, M.15
Bonaconsa, A.16
Mazzoli, M.17
Orzan, E.18
Espeso, A.19
Stephens, D.20
Verbruggen, K.21
Huyghe, J.22
Dhooge, I.23
Huygen, P.24
Kremer, H.25
Cremers, C.W.26
Kunst, S.27
Manninen, M.28
Pyykko, I.29
Lacava, A.30
Steffens, M.31
Wienker, T.F.32
Van Laer, L.33
more..
-
44
-
-
34848875754
-
The contribution of GJB2 (connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss
-
Van Eyken E., Van Laer L., Fransen E., Topsakal V., Hendrickx J.J., Demeester K., Van de Heyning P., Maki-Torkko E., Hannula S., Sorri M., Jensen M., Parving A., Bille M., Baur M., Pfister M., Bonaconsa A., Mazzoli M., Orzan E., Espeso A., Stephens D., Verbruggen K., Huyghe J., Dhooge I., Huygen P., Kremer H., Cremers C., Kunst S., Manninen M., Pyykko I., Rajkowska E., Pawelczyk M., Sliwinska-Kowalska M., Steffens M., Wienker T., Van Camp G. The contribution of GJB2 (connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss. Otol Neurotol. 2007, 28:970-975.
-
(2007)
Otol Neurotol.
, vol.28
, pp. 970-975
-
-
Van Eyken, E.1
Van Laer, L.2
Fransen, E.3
Topsakal, V.4
Hendrickx, J.J.5
Demeester, K.6
Van de Heyning, P.7
Maki-Torkko, E.8
Hannula, S.9
Sorri, M.10
Jensen, M.11
Parving, A.12
Bille, M.13
Baur, M.14
Pfister, M.15
Bonaconsa, A.16
Mazzoli, M.17
Orzan, E.18
Espeso, A.19
Stephens, D.20
Verbruggen, K.21
Huyghe, J.22
Dhooge, I.23
Huygen, P.24
Kremer, H.25
Cremers, C.26
Kunst, S.27
Manninen, M.28
Pyykko, I.29
Rajkowska, E.30
Pawelczyk, M.31
Sliwinska-Kowalska, M.32
Steffens, M.33
Wienker, T.34
Van Camp, G.35
more..
-
45
-
-
38049053663
-
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment
-
Van Laer L., Van Eyken E., Fransen E., Huyghe J.R., Topsakal V., Hendrickx J.J., Hannula S., Maki-Torkko E., Jensen M., Demeester K., Baur M., Bonaconsa A., Mazzoli M., Espeso A., Verbruggen K., Huyghe J., Huygen P., Kunst S., Manninen M., Konings A., Diaz-Lacava A.N., Steffens M., Wienker T.F., Pyykko I., Cremers C.W., Kremer H., Dhooge I., Stephens D., Orzan E., Pfister M., Bille M., Parving A., Sorri M., Van de Heyning P.H., Van Camp G. The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. Hum Mol Genet. 2008, 17:159-169.
-
(2008)
Hum Mol Genet.
, vol.17
, pp. 159-169
-
-
Van Laer, L.1
Van Eyken, E.2
Fransen, E.3
Huyghe, J.R.4
Topsakal, V.5
Hendrickx, J.J.6
Hannula, S.7
Maki-Torkko, E.8
Jensen, M.9
Demeester, K.10
Baur, M.11
Bonaconsa, A.12
Mazzoli, M.13
Espeso, A.14
Verbruggen, K.15
Huyghe, J.16
Huygen, P.17
Kunst, S.18
Manninen, M.19
Konings, A.20
Diaz-Lacava, A.N.21
Steffens, M.22
Wienker, T.F.23
Pyykko, I.24
Cremers, C.W.25
Kremer, H.26
Dhooge, I.27
Stephens, D.28
Orzan, E.29
Pfister, M.30
Bille, M.31
Parving, A.32
Sorri, M.33
Van de Heyning, P.H.34
Van Camp, G.35
more..
-
46
-
-
64049089255
-
Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation
-
Van Oven M., Kayser M. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Hum Mutat. 2009, 30:386-394.
-
(2009)
Hum Mutat.
, vol.30
, pp. 386-394
-
-
Van Oven, M.1
Kayser, M.2
-
47
-
-
34250376913
-
Genetic and environmental influences on hearing in older women
-
Viljanen A., Era P., Kaprio J., Pyykko I., Koskenvuo M., Rantanen T. Genetic and environmental influences on hearing in older women. J Gerontol A Biol Sci Med Sci. 2007, 62:447-452.
-
(2007)
J Gerontol A Biol Sci Med Sci.
, vol.62
, pp. 447-452
-
-
Viljanen, A.1
Era, P.2
Kaprio, J.3
Pyykko, I.4
Koskenvuo, M.5
Rantanen, T.6
-
48
-
-
0031205455
-
Mitochondrial DNA in aging and disease
-
Wallace D.C. Mitochondrial DNA in aging and disease. Sci Am. 1997, 277:40-47.
-
(1997)
Sci Am.
, vol.277
, pp. 40-47
-
-
Wallace, D.C.1
-
49
-
-
70450231612
-
Energetics, epigenetics, mitochondrial genetics
-
Wallace D.C., Fan W.W. Energetics, epigenetics, mitochondrial genetics. Mitochondrion. 2010, 10:12-31.
-
(2010)
Mitochondrion.
, vol.10
, pp. 12-31
-
-
Wallace, D.C.1
Fan, W.W.2
-
50
-
-
0023240790
-
Sequence-analysis of CDNAS for the human and bovine ATP synthase Beta-subunit-mitochondrial-DNA genes sustain 17 more mutations
-
Wallace D.C., Ye J.H., Neckelmann S.N., Singh G., Webster K.A., Greenberg B.D. Sequence-analysis of CDNAS for the human and bovine ATP synthase Beta-subunit-mitochondrial-DNA genes sustain 17 more mutations. Curr Genet. 1987, 12:81-90.
-
(1987)
Curr Genet.
, vol.12
, pp. 81-90
-
-
Wallace, D.C.1
Ye, J.H.2
Neckelmann, S.N.3
Singh, G.4
Webster, K.A.5
Greenberg, B.D.6
-
51
-
-
33947204097
-
Role of mitochondrial dysfunction and mitochondrial DNA mutations in age-related hearing loss
-
Yamasoba T., Someya S., Yamada C., Weindruch R., Prolla T.A., Tanokura M. Role of mitochondrial dysfunction and mitochondrial DNA mutations in age-related hearing loss. Hear Res. 2007, 226:185-193.
-
(2007)
Hear Res.
, vol.226
, pp. 185-193
-
-
Yamasoba, T.1
Someya, S.2
Yamada, C.3
Weindruch, R.4
Prolla, T.A.5
Tanokura, M.6
-
52
-
-
33646185290
-
A reappraisal of complete mtDNA variation in East Asian families with hearing impairment
-
Yao Y.G., Salas A., Bravi C.M., Bandelt H.J. A reappraisal of complete mtDNA variation in East Asian families with hearing impairment. Hum Genet. 2006, 119:505-515.
-
(2006)
Hum Genet.
, vol.119
, pp. 505-515
-
-
Yao, Y.G.1
Salas, A.2
Bravi, C.M.3
Bandelt, H.J.4
-
53
-
-
0036743214
-
Cochlear mitochondrial DNA3867bp deletion in aged mice
-
Zhang X.X., Han D.Y., Ding D.L., Dai P., Yang W.Y., Jiang S.C., Salvi R.J. Cochlear mitochondrial DNA3867bp deletion in aged mice. Chin Med J. 2002, 115:1390-1393.
-
(2002)
Chin Med J.
, vol.115
, pp. 1390-1393
-
-
Zhang, X.X.1
Han, D.Y.2
Ding, D.L.3
Dai, P.4
Yang, W.Y.5
Jiang, S.C.6
Salvi, R.J.7
-
54
-
-
33748623364
-
An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome
-
Zhou S.Y., Kassauei K., Cutler D.J., Kennedy G.C., Sidransky D., Maitra A., Califano J. An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome. J Mol Diagn. 2006, 8:476-482.
-
(2006)
J Mol Diagn.
, vol.8
, pp. 476-482
-
-
Zhou, S.Y.1
Kassauei, K.2
Cutler, D.J.3
Kennedy, G.C.4
Sidransky, D.5
Maitra, A.6
Califano, J.7
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