-
1
-
-
84931815061
-
Uber der verenbung der hereditaren labyrinth-schwerkorigkeit und der otosclerose
-
Albrecht W. Uber der verenbung der hereditaren labyrinth-schwerkorigkeit und der otosclerose. Arch. ohrenheilk. Nas. Kehlkopfheilk 1922, 110:15-48.
-
(1922)
Arch. ohrenheilk. Nas. Kehlkopfheilk
, vol.110
, pp. 15-48
-
-
Albrecht, W.1
-
2
-
-
34447257933
-
Clinical and genetic analysis of two Tunisian otosclerosis families
-
Ali I.B., Thys M., Beltaief N., Schrauwen I., Dieltjens N., Vanderstraeten K., Besbes G., Mnif E., Hachicha S., Arab S.B., Camp G.V. Clinical and genetic analysis of two Tunisian otosclerosis families. Am. J. Med. Genet. A 2007, 143A:1653-1660.
-
(2007)
Am. J. Med. Genet. A
, vol.143 A
, pp. 1653-1660
-
-
Ali, I.B.1
Thys, M.2
Beltaief, N.3
Schrauwen, I.4
Dieltjens, N.5
Vanderstraeten, K.6
Besbes, G.7
Mnif, E.8
Hachicha, S.9
Arab, S.B.10
Camp, G.V.11
-
3
-
-
40449110126
-
No evidence of linkage between 7q33-36 locus (OTSC2) and otosclerosis in seven British Caucasian pedigrees
-
Alzoubi F.Q., Ollier W.R., Ramsden R.T., Saeed S.R. No evidence of linkage between 7q33-36 locus (OTSC2) and otosclerosis in seven British Caucasian pedigrees. J. Laryngol. Otol. 2007, 121:1140-1147.
-
(2007)
J. Laryngol. Otol.
, vol.121
, pp. 1140-1147
-
-
Alzoubi, F.Q.1
Ollier, W.R.2
Ramsden, R.T.3
Saeed, S.R.4
-
4
-
-
0023238691
-
Detection of measles and rubella-specific antigens in the endochondral ossification zone in otosclerosis
-
Arnold W., Friedmann I. Detection of measles and rubella-specific antigens in the endochondral ossification zone in otosclerosis. Laryngol. Rhinol. Otol. (Stuttg) 1987, 66:167-171.
-
(1987)
Laryngol. Rhinol. Otol. (Stuttg)
, vol.66
, pp. 167-171
-
-
Arnold, W.1
Friedmann, I.2
-
5
-
-
0001326145
-
Vererbung und Konstitution bei ohrenkrakheiten
-
Bauer J., Stein C. Vererbung und Konstitution bei ohrenkrakheiten. Z. Konstitutionslehre 1925, 10:483-545.
-
(1925)
Z. Konstitutionslehre
, vol.10
, pp. 483-545
-
-
Bauer, J.1
Stein, C.2
-
6
-
-
41149125972
-
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9
-
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., Van Camp G. A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9. Hum. Genet. 2008, 123:267-272.
-
(2008)
Hum. Genet.
, vol.123
, pp. 267-272
-
-
Bel Hadj Ali, I.1
Thys, M.2
Beltaief, N.3
Schrauwen, I.4
Hilgert, N.5
Vanderstraeten, K.6
Dieltjens, N.7
Mnif, E.8
Hachicha, S.9
Besbes, G.10
Ben Arab, S.11
Van Camp, G.12
-
8
-
-
33645862577
-
Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus
-
Brownstein Z., Goldfarb A., Levi H., Frydman M., Avraham K.B. Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus. Arch. Otolaryngol. Head Neck Surg. 2006, 132:416-424.
-
(2006)
Arch. Otolaryngol. Head Neck Surg.
, vol.132
, pp. 416-424
-
-
Brownstein, Z.1
Goldfarb, A.2
Levi, H.3
Frydman, M.4
Avraham, K.B.5
-
10
-
-
34248347443
-
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis
-
Chen W., Meyer N., McKenna M., Pfister M., McBride D., Fukushima K., Thys M., Camp G., Smith R. Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis. Clin. Genet. 2007, 71:406-414.
-
(2007)
Clin. Genet.
, vol.71
, pp. 406-414
-
-
Chen, W.1
Meyer, N.2
McKenna, M.3
Pfister, M.4
McBride, D.5
Fukushima, K.6
Thys, M.7
Camp, G.8
Smith, R.9
-
11
-
-
18444377048
-
Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3
-
Chen W., Campbell C.A., Green G.E., Van Den Bogaert K., Komodikis C., Manolidis L.S., Aconomou E., Kyamides Y., Christodoulou K., Faghel C., Giguere C.M., Alford R.L., Manolidis S., Van Camp G., Smith R.J. Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21.3-22.3. J. Med. Genet. 2002, 39:473-477.
-
(2002)
J. Med. Genet.
, vol.39
, pp. 473-477
-
-
Chen, W.1
Campbell, C.A.2
Green, G.E.3
Van Den Bogaert, K.4
Komodikis, C.5
Manolidis, L.S.6
Aconomou, E.7
Kyamides, Y.8
Christodoulou, K.9
Faghel, C.10
Giguere, C.M.11
Alford, R.L.12
Manolidis, S.13
Van Camp, G.14
Smith, R.J.15
-
12
-
-
0034854437
-
Prevalence of otosclerosis in an unselected series of temporal bones
-
Declau F., Van Spaendonck M., Timmermans J.P., Michaels L., Liang J., Qiu J.P., Van de Heyning P. Prevalence of otosclerosis in an unselected series of temporal bones. Otol. Neurotol. 2001, 22:596-602.
-
(2001)
Otol. Neurotol.
, vol.22
, pp. 596-602
-
-
Declau, F.1
Van Spaendonck, M.2
Timmermans, J.P.3
Michaels, L.4
Liang, J.5
Qiu, J.P.6
Van de Heyning, P.7
-
13
-
-
33846608691
-
Prevalence of histologic otosclerosis: an unbiased temporal bone study in Caucasians
-
Declau F., van Spaendonck M., Timmermans J.P., Michaels L., Liang J., Qiu J.P., van de Heyning P. Prevalence of histologic otosclerosis: an unbiased temporal bone study in Caucasians. Adv. Otorhinolaryngol. 2007, 65:6-16.
-
(2007)
Adv. Otorhinolaryngol.
, vol.65
, pp. 6-16
-
-
Declau, F.1
Van Spaendonck, M.2
Timmermans, J.P.3
Michaels, L.4
Liang, J.5
Qiu, J.P.6
Van de Heyning, P.7
-
14
-
-
77953682782
-
Etude genetique et localisation d'un gene de l'otospongiose chez les familles Tunisiennes, 106 Congres Francais d'Oto-Rhino-Laryngologie et de Chirurgie de la Face et du Cou
-
Van Den Bogaert et al. 2002, Paris
-
Drira, et al., 1999. Etude genetique et localisation d'un gene de l'otospongiose chez les familles Tunisiennes, 106 Congres Francais d'Oto-Rhino-Laryngologie et de Chirurgie de la Face et du Cou. In: Van Den Bogaert et al. 2002. Bone 30(4), 624-630, Paris.
-
(1999)
Bone
, vol.30
, Issue.4
, pp. 624-630
-
-
Drira et, al.1
-
15
-
-
44649191635
-
Gene expression analysis of human otosclerotic stapedial footplates
-
Ealy M., Chen W., Ryu G.Y., Yoon J.G., Welling D.B., Hansen M., Madan A., Smith R.J. Gene expression analysis of human otosclerotic stapedial footplates. Hear. Res. 2008, 240:80-86.
-
(2008)
Hear. Res.
, vol.240
, pp. 80-86
-
-
Ealy, M.1
Chen, W.2
Ryu, G.Y.3
Yoon, J.G.4
Welling, D.B.5
Hansen, M.6
Madan, A.7
Smith, R.J.8
-
16
-
-
0342751273
-
Estimation of volume referent bone turnover in the otic capsule after sequential point labeling
-
Frisch T., Sorensen M.S., Overgaard S., Bretlau P. Estimation of volume referent bone turnover in the otic capsule after sequential point labeling. Ann. Otol. Rhinol. Laryngol. 2000, 109:33-39.
-
(2000)
Ann. Otol. Rhinol. Laryngol.
, vol.109
, pp. 33-39
-
-
Frisch, T.1
Sorensen, M.S.2
Overgaard, S.3
Bretlau, P.4
-
17
-
-
0029836744
-
Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene
-
Grant S.F., Reid D.M., Blake G., Herd R., Fogelman I., Ralston S.H. Reduced bone density and osteoporosis associated with a polymorphic Sp1 binding site in the collagen type I alpha 1 gene. Nat. Genet. 1996, 14:203-205.
-
(1996)
Nat. Genet.
, vol.14
, pp. 203-205
-
-
Grant, S.F.1
Reid, D.M.2
Blake, G.3
Herd, R.4
Fogelman, I.5
Ralston, S.H.6
-
18
-
-
0020368050
-
HLA antigens and otosclerosis. A possible new genetic factor
-
Gregoriadis S., Zervas J., Varletzidis E., Toubis M., Pantazopoulos P., Fessas P. HLA antigens and otosclerosis. A possible new genetic factor. Arch. Otolaryngol. 1982, 108:769-771.
-
(1982)
Arch. Otolaryngol.
, vol.108
, pp. 769-771
-
-
Gregoriadis, S.1
Zervas, J.2
Varletzidis, E.3
Toubis, M.4
Pantazopoulos, P.5
Fessas, P.6
-
20
-
-
41349121418
-
Relation between renin-angiotensin-aldosterone system and otosclerosis: a genetic association and in vitro study
-
Imauchi Y., Jeunemaitre X., Boussion M., Ferrary E., Sterkers O., Grayeli A.B. Relation between renin-angiotensin-aldosterone system and otosclerosis: a genetic association and in vitro study. Otol. Neurotol. 2008, 29:295-301.
-
(2008)
Otol. Neurotol.
, vol.29
, pp. 295-301
-
-
Imauchi, Y.1
Jeunemaitre, X.2
Boussion, M.3
Ferrary, E.4
Sterkers, O.5
Grayeli, A.B.6
-
21
-
-
4043130443
-
Measles virus prevalence in otosclerotic stapes footplate samples
-
Karosi T., Konya J., Szabo L.Z., Sziklai I. Measles virus prevalence in otosclerotic stapes footplate samples. Otol. Neurotol. 2004, 25:451-456.
-
(2004)
Otol. Neurotol.
, vol.25
, pp. 451-456
-
-
Karosi, T.1
Konya, J.2
Szabo, L.Z.3
Sziklai, I.4
-
22
-
-
34247866321
-
Expression of measles virus receptors in otosclerotic, non-otosclerotic and in normal stapes footplates
-
Karosi T., Jokay I., Konya J., Petko M., Szabo L.Z., Sziklai I. Expression of measles virus receptors in otosclerotic, non-otosclerotic and in normal stapes footplates. Eur. Arch. Otorhinolaryngol. 2007, 264:607-613.
-
(2007)
Eur. Arch. Otorhinolaryngol.
, vol.264
, pp. 607-613
-
-
Karosi, T.1
Jokay, I.2
Konya, J.3
Petko, M.4
Szabo, L.Z.5
Sziklai, I.6
-
23
-
-
51649116682
-
Disease-associated novel CD46 splicing variants and pathologic bone remodeling in otosclerosis
-
Karosi T., Szalmas A., Csomor P., Konya J., Petko M., Sziklai I. Disease-associated novel CD46 splicing variants and pathologic bone remodeling in otosclerosis. Laryngoscope 2008, 118:1669-1676.
-
(2008)
Laryngoscope
, vol.118
, pp. 1669-1676
-
-
Karosi, T.1
Szalmas, A.2
Csomor, P.3
Konya, J.4
Petko, M.5
Sziklai, I.6
-
24
-
-
0028877463
-
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
-
Lander E., Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat. Genet. 1995, 11:241-247.
-
(1995)
Nat. Genet.
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
25
-
-
0002256793
-
Otosclerosis. A genetic and clinical study
-
Larsson A. Otosclerosis. A genetic and clinical study. Acta Otolaryngol. Suppl. 1960, 154:1-86.
-
(1960)
Acta Otolaryngol
, vol.154
, Issue.SUPPL.
, pp. 1-86
-
-
Larsson, A.1
-
26
-
-
26944468241
-
Does pregnancy affect otosclerosis?
-
Lippy W.H., Berenholz L.P., Schuring A.G., Burkey J.M. Does pregnancy affect otosclerosis?. Laryngoscope 2005, 115:1833-1836.
-
(2005)
Laryngoscope
, vol.115
, pp. 1833-1836
-
-
Lippy, W.H.1
Berenholz, L.P.2
Schuring, A.G.3
Burkey, J.M.4
-
27
-
-
84907113981
-
Ultrastructural and immunohistochemical evidence of measles virus in active otosclerosis
-
(discussion 139-140)
-
McKenna M.J., Mills B.G. Ultrastructural and immunohistochemical evidence of measles virus in active otosclerosis. Acta Otolaryngol. Suppl. 1990, 470:130-139. (discussion 139-140).
-
(1990)
Acta Otolaryngol
, vol.470
, Issue.SUPPL.
, pp. 130-139
-
-
McKenna, M.J.1
Mills, B.G.2
-
28
-
-
0036162101
-
Similar COL1A1 expression in fibroblasts from some patients with clinical otosclerosis and those with type I osteogenesis imperfecta
-
McKenna M.J., Kristiansen A.G., Tropitzsch A.S. Similar COL1A1 expression in fibroblasts from some patients with clinical otosclerosis and those with type I osteogenesis imperfecta. Ann. Otol. Rhinol. Laryngol. 2002, 111:184-189.
-
(2002)
Ann. Otol. Rhinol. Laryngol.
, vol.111
, pp. 184-189
-
-
McKenna, M.J.1
Kristiansen, A.G.2
Tropitzsch, A.S.3
-
29
-
-
4043131873
-
Association of otosclerosis with Sp1 binding site polymorphism in COL1A1 gene: evidence for a shared genetic etiology with osteoporosis
-
McKenna M.J., Nguyen-Huynh A.T., Kristiansen A.G. Association of otosclerosis with Sp1 binding site polymorphism in COL1A1 gene: evidence for a shared genetic etiology with osteoporosis. Otol. Neurotol. 2004, 25:447-450.
-
(2004)
Otol. Neurotol.
, vol.25
, pp. 447-450
-
-
McKenna, M.J.1
Nguyen-Huynh, A.T.2
Kristiansen, A.G.3
-
30
-
-
0031689819
-
Association of COL1A1 and otosclerosis: evidence for a shared genetic etiology with mild osteogenesis imperfecta
-
McKenna M.J., Kristiansen A.G., Bartley M.L., Rogus J.J., Haines J.L. Association of COL1A1 and otosclerosis: evidence for a shared genetic etiology with mild osteogenesis imperfecta. Am. J. Otol. 1998, 19:604-610.
-
(1998)
Am. J. Otol.
, vol.19
, pp. 604-610
-
-
McKenna, M.J.1
Kristiansen, A.G.2
Bartley, M.L.3
Rogus, J.J.4
Haines, J.L.5
-
31
-
-
0014117560
-
Genetic factors in otosclerosis
-
Morrison A.W. Genetic factors in otosclerosis. Ann. R. Coll. Surg. Engl. 1967, 41:202-237.
-
(1967)
Ann. R. Coll. Surg. Engl.
, vol.41
, pp. 202-237
-
-
Morrison, A.W.1
-
32
-
-
0014466604
-
Histopathology of otosclerosis
-
Nager G.T. Histopathology of otosclerosis. Arch. Otolaryngol. 1969, 89:341-363.
-
(1969)
Arch. Otolaryngol.
, vol.89
, pp. 341-363
-
-
Nager, G.T.1
-
33
-
-
0024234621
-
Osteogenesis imperfecta of the temporal bone and its relation to otosclerosis
-
Nager G.T. Osteogenesis imperfecta of the temporal bone and its relation to otosclerosis. Ann. Otol. Rhinol. Laryngol. 1988, 97:585-593.
-
(1988)
Ann. Otol. Rhinol. Laryngol.
, vol.97
, pp. 585-593
-
-
Nager, G.T.1
-
34
-
-
0028289265
-
Evidence of measles virus RNA in otosclerotic tissue
-
Niedermeyer H., Arnold W., Neubert W.J., Hofler H. Evidence of measles virus RNA in otosclerotic tissue. ORL J. Otorhinolaryngol. Relat. Spec. 1994, 56:130-132.
-
(1994)
ORL J. Otorhinolaryngol. Relat. Spec.
, vol.56
, pp. 130-132
-
-
Niedermeyer, H.1
Arnold, W.2
Neubert, W.J.3
Hofler, H.4
-
35
-
-
0000274171
-
Uber primare erkrankung der knockernen labyrinthkapsel
-
Politzer A. Uber primare erkrankung der knockernen labyrinthkapsel. Zeitschrift Fur Ohrenheilkunde 1894, 25:309-327.
-
(1894)
Zeitschrift Fur Ohrenheilkunde
, vol.25
, pp. 309-327
-
-
Politzer, A.1
-
36
-
-
0037016683
-
Reelin is a serine protease of the extracellular matrix
-
Quattrocchi C.C., Wannenes F., Persico A.M., Ciafre S.A., D'Arcangelo G., Farace M.G., Keller F. Reelin is a serine protease of the extracellular matrix. J. Biol. Chem. 2002, 277:303-309.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 303-309
-
-
Quattrocchi, C.C.1
Wannenes, F.2
Persico, A.M.3
Ciafre, S.A.4
D'Arcangelo, G.5
Farace, M.G.6
Keller, F.7
-
37
-
-
0028246134
-
Mixed hearing loss in otosclerosis: indication for long-term follow-up
-
Ramsay H.A., Linthicum F.H. Mixed hearing loss in otosclerosis: indication for long-term follow-up. Am. J. Otol. 1994, 15:536-539.
-
(1994)
Am. J. Otol.
, vol.15
, pp. 536-539
-
-
Ramsay, H.A.1
Linthicum, F.H.2
-
38
-
-
3042846789
-
Proposed association between the COL1A1 and COL1A2 genes and otosclerosis is not supported by a case-control study in Spain
-
Rodriguez L., Rodriguez S., Hermida J., Frade C., Sande E., Visedo G., Martin C., Zapata C. Proposed association between the COL1A1 and COL1A2 genes and otosclerosis is not supported by a case-control study in Spain. Am. J. Med. Genet. A 2004, 128:19-22.
-
(2004)
Am. J. Med. Genet. A
, vol.128
, pp. 19-22
-
-
Rodriguez, L.1
Rodriguez, S.2
Hermida, J.3
Frade, C.4
Sande, E.5
Visedo, G.6
Martin, C.7
Zapata, C.8
-
39
-
-
74349124278
-
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch population
-
2009 Jun 5 [Epub ahead of print]
-
Schrauwen I., Thys M., Vanderstraeten K., Fransen E., Ealy M., Cremers C.W., Dhooge I., Van de Heyning P., Offeciers E., Smith R.J., Van Camp G. No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch population. Otol. Neurotol. 2009, 2009 Jun 5 [Epub ahead of print].
-
(2009)
Otol. Neurotol.
-
-
Schrauwen, I.1
Thys, M.2
Vanderstraeten, K.3
Fransen, E.4
Ealy, M.5
Cremers, C.W.6
Dhooge, I.7
Van de Heyning, P.8
Offeciers, E.9
Smith, R.J.10
Van Camp, G.11
-
40
-
-
61849109303
-
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis
-
Schrauwen I., Ealy M., Huentelman M.J., Thys M., Homer N., Vanderstraeten K., Fransen E., Corneveaux J.J., Craig D.W., Claustres M., Cremers C.W., Dhooge I., Van de Heyning P., Vincent R., Offeciers E., Smith R.J., Van Camp G. A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. Am. J. Hum. Genet. 2009, 84:328-338.
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 328-338
-
-
Schrauwen, I.1
Ealy, M.2
Huentelman, M.J.3
Thys, M.4
Homer, N.5
Vanderstraeten, K.6
Fransen, E.7
Corneveaux, J.J.8
Craig, D.W.9
Claustres, M.10
Cremers, C.W.11
Dhooge, I.12
Van de Heyning, P.13
Vincent, R.14
Offeciers, E.15
Smith, R.J.16
Van Camp, G.17
-
41
-
-
41849127482
-
Association of bone morphogenetic proteins with otosclerosis
-
Schrauwen I., Thys M., Vanderstraeten K., Fransen E., Dieltjens N., Huyghe J.R., Ealy M., Claustres M., Cremers C.R., Dhooge I., Declau F., Van de Heyning P., Vincent R., Somers T., Offeciers E., Smith R.J., Van Camp G. Association of bone morphogenetic proteins with otosclerosis. J. Bone Miner. Res. 2008, 23:507-516.
-
(2008)
J. Bone Miner. Res.
, vol.23
, pp. 507-516
-
-
Schrauwen, I.1
Thys, M.2
Vanderstraeten, K.3
Fransen, E.4
Dieltjens, N.5
Huyghe, J.R.6
Ealy, M.7
Claustres, M.8
Cremers, C.R.9
Dhooge, I.10
Declau, F.11
Van de Heyning, P.12
Vincent, R.13
Somers, T.14
Offeciers, E.15
Smith, R.J.16
Van Camp, G.17
-
42
-
-
0023275558
-
Pregnancy: an overfill or underfill state
-
Schrier R.W., Durr J.A. Pregnancy: an overfill or underfill state. Am. J. Kidney Dis. 1987, 9:284-289.
-
(1987)
Am. J. Kidney Dis.
, vol.9
, pp. 284-289
-
-
Schrier, R.W.1
Durr, J.A.2
-
44
-
-
0347855674
-
Totaler knocherner verschless beider labyrinthfester und labyrinthitis serosa infolage progressiver spongiosierung
-
Siebenmann F. Totaler knocherner verschless beider labyrinthfester und labyrinthitis serosa infolage progressiver spongiosierung. Verhanlungen Deutschen Otologischenn Gesellschaft 6 1912.
-
(1912)
Verhanlungen Deutschen Otologischenn Gesellschaft 6
-
-
Siebenmann, F.1
-
45
-
-
60549089067
-
Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients
-
Thys M., Schrauwen I., Vanderstraeten K., Dieltjens N., Fransen E., Ealy M., Cremers C.W., van de Heyning P., Vincent R., Offeciers E., Smith R.H., van Camp G. Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients. Ann. Hum. Genet. 2009, 73:171-175.
-
(2009)
Ann. Hum. Genet.
, vol.73
, pp. 171-175
-
-
Thys, M.1
Schrauwen, I.2
Vanderstraeten, K.3
Dieltjens, N.4
Fransen, E.5
Ealy, M.6
Cremers, C.W.7
van de Heyning, P.8
Vincent, R.9
Offeciers, E.10
Smith, R.H.11
van Camp, G.12
-
46
-
-
33847227351
-
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1
-
Thys M., Van Den Bogaert K., Iliadou V., Vanderstraeten K., Dieltjens N., Schrauwen I., Chen W., Eleftheriades N., Grigoriadou M., Pauw R.J., Cremers C.R., Smith R.J., Petersen M.B., Van Camp G. A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1. Eur. J. Hum. Genet. 2007, 15:362-368.
-
(2007)
Eur. J. Hum. Genet.
, vol.15
, pp. 362-368
-
-
Thys, M.1
Van Den Bogaert, K.2
Iliadou, V.3
Vanderstraeten, K.4
Dieltjens, N.5
Schrauwen, I.6
Chen, W.7
Eleftheriades, N.8
Grigoriadou, M.9
Pauw, R.J.10
Cremers, C.R.11
Smith, R.J.12
Petersen, M.B.13
Van Camp, G.14
-
47
-
-
34548426475
-
The coding polymorphism T263I in TGF-{beta}1 is associated with otosclerosis in two independent populations
-
Thys M., Schrauwen I., Vanderstraeten K., Janssens K., Dieltjens N., Van Den Bogaert K., Fransen E., Chen W., Ealy M., Claustres M., Cremers C.R., Dhooge I., Declau F., Claes J., Van de Heyning P., Vincent R., Somers T., Offeciers E., Smith R.J., Van Camp G. The coding polymorphism T263I in TGF-{beta}1 is associated with otosclerosis in two independent populations. Hum. Mol. Genet. 2007, 16:2021-2030.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 2021-2030
-
-
Thys, M.1
Schrauwen, I.2
Vanderstraeten, K.3
Janssens, K.4
Dieltjens, N.5
Van Den Bogaert, K.6
Fransen, E.7
Chen, W.8
Ealy, M.9
Claustres, M.10
Cremers, C.R.11
Dhooge, I.12
Declau, F.13
Claes, J.14
Van de Heyning, P.15
Vincent, R.16
Somers, T.17
Offeciers, E.18
Smith, R.J.19
Van Camp, G.20
more..
-
48
-
-
6844251602
-
Localization of a gene for otosclerosis to chromosome 15q25-q26
-
Tomek M.S., Brown M.R., Mani S.R., Ramesh A., Srisailapathy C.R., Coucke P., Zbar R.I., Bell A.M., McGuirt W.T., Fukushima K., Willems P.J., Van Camp G., Smith R.J. Localization of a gene for otosclerosis to chromosome 15q25-q26. Hum. Mol. Genet. 1998, 7:285-290.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 285-290
-
-
Tomek, M.S.1
Brown, M.R.2
Mani, S.R.3
Ramesh, A.4
Srisailapathy, C.R.5
Coucke, P.6
Zbar, R.I.7
Bell, A.M.8
McGuirt, W.T.9
Fukushima, K.10
Willems, P.J.11
Van Camp, G.12
Smith, R.J.13
-
49
-
-
0008274624
-
Pathological and surgical observations on the disease of the ear
-
Toynbee J. Pathological and surgical observations on the disease of the ear. Med. Chir. Trans. 1861, 24:109-205.
-
(1861)
Med. Chir. Trans.
, vol.24
, pp. 109-205
-
-
Toynbee, J.1
-
50
-
-
2942755753
-
A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24
-
Van Den Bogaert K., De Leenheer E.M., Chen W., Lee Y., Nurnberg P., Pennings R.J., Vanderstraeten K., Thys M., Cremers C.W., Smith R.J., Van Camp G. A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24. J. Med. Genet. 2004, 41:450-453.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 450-453
-
-
Van Den Bogaert, K.1
De Leenheer, E.M.2
Chen, W.3
Lee, Y.4
Nurnberg, P.5
Pennings, R.J.6
Vanderstraeten, K.7
Thys, M.8
Cremers, C.W.9
Smith, R.J.10
Van Camp, G.11
-
51
-
-
0035121870
-
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36
-
Van Den Bogaert K., Govaerts P.J., Schatteman I., Brown M.R., Caethoven G., Offeciers F.E., Somers T., Declau F., Coucke P., Van de Heyning P., Smith R.J., Van Camp G. A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36. Am. J. Hum. Genet. 2001, 68:495-500.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 495-500
-
-
Van Den Bogaert, K.1
Govaerts, P.J.2
Schatteman, I.3
Brown, M.R.4
Caethoven, G.5
Offeciers, F.E.6
Somers, T.7
Declau, F.8
Coucke, P.9
Van de Heyning, P.10
Smith, R.J.11
Van Camp, G.12
-
52
-
-
0036207779
-
Otosclerosis: a genetically heterogeneous disease involving at least three different genes
-
Van Den Bogaert K., Govaerts P.J., De Leenheer E.M., Schatteman I., Verstreken M., Chen W., Declau F., Cremers C.W., Van De Heyning P.H., Offeciers F.E., Somers T., Smith R.J., Van Camp G. Otosclerosis: a genetically heterogeneous disease involving at least three different genes. Bone 2002, 30:624-630.
-
(2002)
Bone
, vol.30
, pp. 624-630
-
-
Van Den Bogaert, K.1
Govaerts, P.J.2
De Leenheer, E.M.3
Schatteman, I.4
Verstreken, M.5
Chen, W.6
Declau, F.7
Cremers, C.W.8
Van De Heyning, P.H.9
Offeciers, F.E.10
Somers, T.11
Smith, R.J.12
Van Camp, G.13
-
53
-
-
0028050102
-
Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagen
-
Willing M.C., Deschenes S.P., Scott D.A., Byers P.H., Slayton R.L., Pitts S.H., Arikat H., Roberts E.J. Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagen. Am. J. Hum. Genet. 1994, 55:638-647.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 638-647
-
-
Willing, M.C.1
Deschenes, S.P.2
Scott, D.A.3
Byers, P.H.4
Slayton, R.L.5
Pitts, S.H.6
Arikat, H.7
Roberts, E.J.8
-
54
-
-
0026410818
-
Hearing impairment in mice with the cmd/cmd (cartilage matrix deficiency) mutant gene
-
Yoo T.J., Cho H., Yamada Y. Hearing impairment in mice with the cmd/cmd (cartilage matrix deficiency) mutant gene. Ann. N. Y. Acad. Sci. 1991, 630:265-267.
-
(1991)
Ann. N. Y. Acad. Sci.
, vol.630
, pp. 265-267
-
-
Yoo, T.J.1
Cho, H.2
Yamada, Y.3
|