-
1
-
-
1542378083
-
The genetic component of middle ear disease in the first 5 years of life
-
Casselbrant ML, Mandel EM, Rockette HE, et al. The genetic component of middle ear disease in the first 5 years of life. Arch Otolaryngol Head Neck Surg 2004; 130:273-278. An excellent follow up to this group's landmark paper published in 1999 clearly showing that susceptibility to otitis media has a genetic component.
-
(2004)
Arch Otolaryngol Head Neck Surg
, vol.130
, pp. 273-278
-
-
Casselbrant, M.L.1
Mandel, E.M.2
Rockette, H.E.3
-
2
-
-
4143083822
-
Genetics of asthma and COPD: Similar results for different phenotypes
-
discussion 159S-161S
-
Meyers DA, Larj MJ, Lange L. Genetics of asthma and COPD: similar results for different phenotypes. Chest 2004; 126(2 Suppl):105S-110S; discussion 159S-161S.
-
(2004)
Chest
, vol.126
, Issue.2 SUPPL.
-
-
Meyers, D.A.1
Larj, M.J.2
Lange, L.3
-
3
-
-
4744342323
-
Atopic dermatitis: A total genome-scan for susceptibility genes
-
Haagerup A, Bjerke T, Schiotz PO, et al. Atopic dermatitis: a total genome-scan for susceptibility genes. Acta Derm Venereol 2004; 84:346-352. This paper demonstrates the power of modern molecular techniques in searching for genes associated with common diseases.
-
(2004)
Acta Derm Venereol
, vol.84
, pp. 346-352
-
-
Haagerup, A.1
Bjerke, T.2
Schiotz, P.O.3
-
5
-
-
12944278908
-
The sudden infant death syndrome gene: Does it exist?
-
Opdal SH, Rognum TO. The sudden infant death syndrome gene: does it exist? Pediatrics 2004; 114:e506-e512. A thoughtful discussion of a syndrome that is polygenic, with both medical and legal consequences.
-
(2004)
Pediatrics
, vol.114
-
-
Opdal, S.H.1
Rognum, T.O.2
-
6
-
-
4243128354
-
'The marvellous harmony of the nervous parts': The origins of multiple sclerosis
-
Compston A. 'The marvellous harmony of the nervous parts': the origins of multiple sclerosis. Clin Med 2004; 4:346-354.
-
(2004)
Clin Med
, vol.4
, pp. 346-354
-
-
Compston, A.1
-
7
-
-
4644328047
-
The role of environmental tobacco smoke in genetic susceptibility to asthma
-
Kurz T, Ober C. The role of environmental tobacco smoke in genetic susceptibility to asthma. Curr Opin Allergy Clin Immunol 2004; 4:335-339.
-
(2004)
Curr Opin Allergy Clin Immunol
, vol.4
, pp. 335-339
-
-
Kurz, T.1
Ober, C.2
-
8
-
-
4644250957
-
Genetic susceptibility to ozone-induced lung inflammation in animal models of asthma
-
Backus-Hazzard GS, Howden R, Kleeberger SR. Genetic susceptibility to ozone-induced lung inflammation in animal models of asthma. Curr Opin Allergy Clin Immunol 2004; 4:349-353. This paper summarizes the work that expanded our concept of what constitutes a genetic susceptibility.
-
(2004)
Curr Opin Allergy Clin Immunol
, vol.4
, pp. 349-353
-
-
Backus-Hazzard, G.S.1
Howden, R.2
Kleeberger, S.R.3
-
9
-
-
4344675699
-
A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage
-
Thompson SD, Moroldo MB, Guyer L, et al. A genome-wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage. Arthritis Rheum 2004; 50:2920-2930.
-
(2004)
Arthritis Rheum
, vol.50
, pp. 2920-2930
-
-
Thompson, S.D.1
Moroldo, M.B.2
Guyer, L.3
-
10
-
-
0042329962
-
Demographic and phenotypic features of 70 families segregating Barrett's oesophagus and oesophageal adenocarcinoma
-
Drovdlic CM, Goddard KA, Chak A, et al. Demographic and phenotypic features of 70 families segregating Barrett's oesophagus and oesophageal adenocarcinoma. J Med Genet 2003; 40:651-656.
-
(2003)
J Med Genet
, vol.40
, pp. 651-656
-
-
Drovdlic, C.M.1
Goddard, K.A.2
Chak, A.3
-
11
-
-
0021808736
-
Familial gastroesophageal reflux and development of Barrett's esophagus
-
Crabb DW, Berk MA, Hall TR, et al. Familial gastroesophageal reflux and development of Barrett's esophagus. Ann Intern Med 1985; 103:52-54.
-
(1985)
Ann Intern Med
, vol.103
, pp. 52-54
-
-
Crabb, D.W.1
Berk, M.A.2
Hall, T.R.3
-
12
-
-
0036191275
-
Familial factors in the etiology of gastroesophageal reflux disease, Barrett's esophagus, and esophageal adenocarcinoma
-
Trudgill N. Familial factors in the etiology of gastroesophageal reflux disease, Barrett's esophagus, and esophageal adenocarcinoma. Chest Surg Clin N Am 2002; 12:15-24.
-
(2002)
Chest Surg Clin N Am
, vol.12
, pp. 15-24
-
-
Trudgill, N.1
-
13
-
-
0036140724
-
Gastroesophageal reflux disease in monozygotic and dizygotic twins
-
Cameron AJ, Lagergren J, Henriksson C, et al. Gastroesophageal reflux disease in monozygotic and dizygotic twins. Gastroenterology 2002; 122:55-59.
-
(2002)
Gastroenterology
, vol.122
, pp. 55-59
-
-
Cameron, A.J.1
Lagergren, J.2
Henriksson, C.3
-
14
-
-
0038298411
-
Genetic influences in gastro-oesophageal reflux disease: A twin study
-
Mohammed I, Cherkas LF, Riley SA, et al. Genetic influences in gastro-oesophageal reflux disease: a twin study. Gut 2003; 52:1085-1089.
-
(2003)
Gut
, vol.52
, pp. 1085-1089
-
-
Mohammed, I.1
Cherkas, L.F.2
Riley, S.A.3
-
15
-
-
0343962635
-
Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14
-
Hu FZ, Preston RA, Post JC, et al. Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14. JAMA 2000; 284:325-334.
-
(2000)
JAMA
, vol.284
, pp. 325-334
-
-
Hu, F.Z.1
Preston, R.A.2
Post, J.C.3
-
16
-
-
0034534303
-
Refined localization of a gene for pediatric gastroesophageal reflux makes HTR2A an unlikely candidate gene
-
Hu FZ, Post JC, Johnson S, et al. Refined localization of a gene for pediatric gastroesophageal reflux makes HTR2A an unlikely candidate gene. Hum Genet 2000; 107:519-525.
-
(2000)
Hum Genet
, vol.107
, pp. 519-525
-
-
Hu, F.Z.1
Post, J.C.2
Johnson, S.3
-
17
-
-
2942752025
-
Fine mapping a gene for pediatric gastroesophageal reflux on human chromosome 13q14
-
Hu FZ, Donfack J, Ahmed A, et al. Fine mapping a gene for pediatric gastroesophageal reflux on human chromosome 13q14. Hum Genet 2004; 114:562-572. The most recent paper describing the process of closing in on GERD1.
-
(2004)
Hum Genet
, vol.114
, pp. 562-572
-
-
Hu, F.Z.1
Donfack, J.2
Ahmed, A.3
-
18
-
-
0036839982
-
Autosomal dominant infantile gastroesophageal reflux disease: Exclusion of a 13q14 locus in five well characterized families
-
Orenstein SR, Shalaby TM, Finch R, et al. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families. Am J Gastroenterol 2002; 97:2725-2732.
-
(2002)
Am J Gastroenterol
, vol.97
, pp. 2725-2732
-
-
Orenstein, S.R.1
Shalaby, T.M.2
Finch, R.3
-
19
-
-
0041385594
-
A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24
-
Kok C, Kennerson ML, Spring PJ, et al. A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24. Am J Hum Genet 2003; 73:632-637.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 632-637
-
-
Kok, C.1
Kennerson, M.L.2
Spring, P.J.3
-
20
-
-
0033069503
-
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy
-
Seri M, Cusano R, Forabosco P, et al. Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy. Am J Hum Genet 1999; 64:586-593.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 586-593
-
-
Seri, M.1
Cusano, R.2
Forabosco, P.3
-
22
-
-
0037110930
-
Gastrointestinal complications of Russell-Silver syndrome: A pilot study
-
Anderson J, Viskochil D, O'Gorman M, Gonzales C. Gastrointestinal complications of Russell-Silver syndrome: a pilot study. Am J Med Genet 2002; 113:15-19.
-
(2002)
Am J Med Genet
, vol.113
, pp. 15-19
-
-
Anderson, J.1
Viskochil, D.2
O'Gorman, M.3
Gonzales, C.4
-
23
-
-
18244389962
-
Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome
-
Nakabayashi K, Fernandez BA, Teshima I, et al. Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome. Genomics 2002; 79:186-196.
-
(2002)
Genomics
, vol.79
, pp. 186-196
-
-
Nakabayashi, K.1
Fernandez, B.A.2
Teshima, I.3
-
24
-
-
0037816227
-
Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism
-
Charalambous M, Smith FM, Bennett WR, et al. Disruption of the imprinted Grb10 gene leads to disproportionate overgrowth by an Igf2-independent mechanism. Proc Natl Acad Sci U S A 2003; 100:8292-8297.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 8292-8297
-
-
Charalambous, M.1
Smith, F.M.2
Bennett, W.R.3
-
26
-
-
4544245238
-
The 'duty to warn' a patient's family members about hereditary disease risks
-
Offit K, Groeger E, Turner S, et al. The 'duty to warn' a patient's family members about hereditary disease risks. JAMA 2004; 292:1469-1473. As advances are made in genetic testing, health care providers will need to become more adept at genetic counseling of patients and families. This paper is a clear discussion of a potential pitfall that may not be particularly obvious to the nongenetics counselor.
-
(2004)
JAMA
, vol.292
, pp. 1469-1473
-
-
Offit, K.1
Groeger, E.2
Turner, S.3
|