-
1
-
-
0033942762
-
Estimation of variance components of quantitative traits in inbred populations
-
Abney M, McPeek. MS, Ober C. 2000. Estimation of variance components of quantitative traits in inbred populations. Am J Hum Genet. 66(2):629-650.
-
(2000)
Am J Hum Genet
, vol.66
, Issue.2
, pp. 629-650
-
-
Abney, M.1
McPeek, M.S.2
Ober, C.3
-
2
-
-
0036201581
-
Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: Fasting serum-insulin level in the Hutterites
-
Abney M, Ober C, McPeek MS. 2002. Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: Fasting serum-insulin level in the Hutterites. Am J Hum Genet. 70(4):920-934.
-
(2002)
Am J Hum Genet
, vol.70
, Issue.4
, pp. 920-934
-
-
Abney, M.1
Ober, C.2
McPeek, M.S.3
-
3
-
-
0031966480
-
Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster County
-
Agarwala R, Biesecker LG, Hopkins KA, Francomanco CA, Schaffer AA. 1998. Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster County. Genome Res. 8(3):211-221.
-
(1998)
Genome Res
, vol.8
, Issue.3
, pp. 211-221
-
-
Agarwala, R.1
Biesecker, L.G.2
Hopkins, K.A.3
Francomanco, C.A.4
Schaffer, A.A.5
-
4
-
-
0142104970
-
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome
-
Ansley SJ, Badano JL, Blacque OE, Hill J, Hoskins BE, Leitch CC, Kim JC, Ross AJ, Eichers ER, Teslovich TM, et al. 2003. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome. Nature. 425(6958):628-633.
-
(2003)
Nature
, vol.425
, Issue.6958
, pp. 628-633
-
-
Ansley, S.J.1
Badano, J.L.2
Blacque, O.E.3
Hill, J.4
Hoskins, B.E.5
Leitch, C.C.6
Kim, J.C.7
Ross, A.J.8
Eichers, E.R.9
Teslovich, T.M.10
-
5
-
-
0037371508
-
Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2
-
Badano JL, Ansley SJ, Leitch CC, Lewis RA, Lupski JR, Katsanis N. 2003. Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2. Am J Hum Genet. 72(3):650-658.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.3
, pp. 650-658
-
-
Badano, J.L.1
Ansley, S.J.2
Leitch, C.C.3
Lewis, R.A.4
Lupski, J.R.5
Katsanis, N.6
-
6
-
-
0026642442
-
Brief report: Intragenic deletion of the KALIG-1 gene in Kallmann's syndrome
-
Bick D, Franco B, Sherins RJ, Heye B, Pike L, Crawford J, Maddalena A, Inceni B, Pragliola A, Meitinger T, et al. 1992. Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome. N Engl J Med. 326(26):1752-1755.
-
(1992)
N Engl J Med
, vol.326
, Issue.26
, pp. 1752-1755
-
-
Bick, D.1
Franco, B.2
Sherins, R.J.3
Heye, B.4
Pike, L.5
Crawford, J.6
Maddalena, A.7
Inceni, B.8
Pragliola, A.9
Meitinger, T.10
-
7
-
-
0042387785
-
Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus
-
Bourgain C, Hoffjan S, Nicolae R, Newman D, Steiner L, Walker K, Reynolds R, Ober C, McPeek MS. 2003. Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus. Am J Hum Genet. 73(3):612-626.
-
(2003)
Am J Hum Genet
, vol.73
, Issue.3
, pp. 612-626
-
-
Bourgain, C.1
Hoffjan, S.2
Nicolae, R.3
Newman, D.4
Steiner, L.5
Walker, K.6
Reynolds, R.7
Ober, C.8
McPeek, M.S.9
-
8
-
-
33646562887
-
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)
-
Chiang AP, Beck JS, Yen HJ, Tayeh MK, Scheetz TE, Swiderski RE, Nishimura DY, Braun TA, Kim KY, Huang J, et al. 2006. Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). Proc Natl Acad Sci USA. 103(16):6287-6292.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, Issue.16
, pp. 6287-6292
-
-
Chiang, A.P.1
Beck, J.S.2
Yen, H.J.3
Tayeh, M.K.4
Scheetz, T.E.5
Swiderski, R.E.6
Nishimura, D.Y.7
Braun, T.A.8
Kim, K.Y.9
Huang, J.10
-
9
-
-
4143115620
-
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)
-
Chiang AP, Nishimura D, Searby C, Elbedour K, Carmi R, Ferguson AL, Secrist J, Braun T, Casavant T, Stone EM, et al. 2004. Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3). Am J Hum Genet. 75(3):475-484.
-
(2004)
Am J Hum Genet
, vol.75
, Issue.3
, pp. 475-484
-
-
Chiang, A.P.1
Nishimura, D.2
Searby, C.3
Elbedour, K.4
Carmi, R.5
Ferguson, A.L.6
Secrist, J.7
Braun, T.8
Casavant, T.9
Stone, E.M.10
-
10
-
-
0027520809
-
Hyposmia in allergic rhinitis
-
Cowart BJ, Flynn-Rodden K, McGeady SJ, Lowry LD. 1993. Hyposmia in allergic rhinitis. J Allergy Clin Immunol. 91(3):747-751.
-
(1993)
J Allergy Clin Immunol
, vol.91
, Issue.3
, pp. 747-751
-
-
Cowart, B.J.1
Flynn-Rodden, K.2
McGeady, S.J.3
Lowry, L.D.4
-
11
-
-
0141814637
-
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
-
de Roux N, Genin E, Carel JC, Matsuda F, Chaussain JL, Milgrom E. 2003. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc Natl Acad Sci USA. 100(19): 10972-10976.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.19
, pp. 10972-10976
-
-
de Roux, N.1
Genin, E.2
Carel, J.C.3
Matsuda, F.4
Chaussain, J.L.5
Milgrom, E.6
-
12
-
-
20244366799
-
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
-
Dodé C, Levilliers J, Dupont JM, De Paepe A, Le Dû N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, et al. 2003. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet. 33(4):463-465.
-
(2003)
Nat Genet
, vol.33
, Issue.4
, pp. 463-465
-
-
Dodé, C.1
Levilliers, J.2
Dupont, J.M.3
De Paepe, A.4
Le Dû, N.5
Soussi-Yanicostas, N.6
Coimbra, R.S.7
Delmaghani, S.8
Compain-Nouaille, S.9
Baverel, F.10
-
13
-
-
0033625390
-
HLA-DRB1 01 alleles are associated with sensitization to cockroach allergens
-
Donfack J, Tsalenko A, Hoki DM, Parry R, Solway J, Lester LA, Ober C. 2000. HLA-DRB1 01 alleles are associated with sensitization to cockroach allergens. J Allergy Clin Immunol. 105(5):960-966.
-
(2000)
J Allergy Clin Immunol
, vol.105
, Issue.5
, pp. 960-966
-
-
Donfack, J.1
Tsalenko, A.2
Hoki, D.M.3
Parry, R.4
Solway, J.5
Lester, L.A.6
Ober, C.7
-
14
-
-
0023765129
-
Olfactory dysfunction in parkinsonism: A general deficit unrelated to neurologic signs, disease stage, or disease duration
-
Doty RL, Deems DA, Frye RE, Pelberg R, Shapiro A. 1988. Olfactory dysfunction in parkinsonism: A general deficit unrelated to neurologic signs, disease stage, or disease duration. Neurology. 38(8):1237-1244.
-
(1988)
Neurology
, vol.38
, Issue.8
, pp. 1237-1244
-
-
Doty, R.L.1
Deems, D.A.2
Frye, R.E.3
Pelberg, R.4
Shapiro, A.5
-
15
-
-
0022510229
-
Quantitative assessment of olfactory function in an industrial setting
-
Doty RL, Gregor T, Monroe C. 1986. Quantitative assessment of olfactory function in an industrial setting. J Occup Med. 28(6):457-460.
-
(1986)
J Occup Med
, vol.28
, Issue.6
, pp. 457-460
-
-
Doty, R.L.1
Gregor, T.2
Monroe, C.3
-
16
-
-
0029976127
-
Development of the 12-item Cross-Cultural Smell Identfication Test (CC-SIT)
-
Doty RL, Marcus A, Lee WW. 1996. Development of the 12-item Cross-Cultural Smell Identfication Test (CC-SIT). Laryngoscope. 106(3 Pt 1): 353-356.
-
(1996)
Laryngoscope
, vol.106
, Issue.3 PART 1
, pp. 353-356
-
-
Doty, R.L.1
Marcus, A.2
Lee, W.W.3
-
17
-
-
0029560592
-
A study of the test-retest reliability of ten olfactory tests
-
Doty RL, McKeown DA, Lee WW, Shaman P. 1995. A study of the test-retest reliability of ten olfactory tests. Chem Senses: 20(6):645-656.
-
(1995)
Chem Senses
, vol.20
, Issue.6
, pp. 645-656
-
-
Doty, R.L.1
McKeown, D.A.2
Lee, W.W.3
Shaman, P.4
-
18
-
-
0021708157
-
Smell identification ability: Changes with age
-
Doty RL, Shaman P, Applebaum SL, Giberson R, Siksorski L, Rosenberg L. 1984. Smell identification ability: Changes with age. Science. 226(4681): 1441-1443.
-
(1984)
Science
, vol.226
, Issue.4681
, pp. 1441-1443
-
-
Doty, R.L.1
Shaman, P.2
Applebaum, S.L.3
Giberson, R.4
Siksorski, L.5
Rosenberg, L.6
-
19
-
-
2342541861
-
Bardet-Biedl syndrome 1 genotype and obesity in the Newfoundland population
-
Fan Y, Rahman P, Peddle L, Hefferton D, Gladney N, Moore SJ, Green JS, Parfrey PS, Davidson WS. 2004. Bardet-Biedl syndrome 1 genotype and obesity in the Newfoundland population. Int J Obes Relat Metab Disord. 28(5):680-684.
-
(2004)
Int J Obes Relat Metab Disord
, vol.28
, Issue.5
, pp. 680-684
-
-
Fan, Y.1
Rahman, P.2
Peddle, L.3
Hefferton, D.4
Gladney, N.5
Moore, S.J.6
Green, J.S.7
Parfrey, P.S.8
Davidson, W.S.9
-
21
-
-
0019852731
-
Ketone compound smelling ability: Study in Hungarian twins
-
Forrai G, Bánkövl G, Szabados T, Papp ES. 1981. Ketone compound smelling ability: Study in Hungarian twins. Acta Med Acad Sci. Hung. 38(2): 153-158.
-
(1981)
Acta Med Acad Sci. Hung
, vol.38
, Issue.2
, pp. 153-158
-
-
Forrai, G.1
Bánkövl, G.2
Szabados, T.3
Papp, E.S.4
-
22
-
-
0025938481
-
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
-
Franco B, Guioli S, Pragliola A, Incerti B, Bardoni B, Tohlorenzi R, Carrozzo R, Maestrini E, Pieretti M, Taillon-Miller P, et al. 1991. A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature. 353(6344): 529-536.
-
(1991)
Nature
, vol.353
, Issue.6344
, pp. 529-536
-
-
Franco, B.1
Guioli, S.2
Pragliola, A.3
Incerti, B.4
Bardoni, B.5
Tohlorenzi, R.6
Carrozzo, R.7
Maestrini, E.8
Pieretti, M.9
Taillon-Miller, P.10
-
23
-
-
0025069860
-
Dose-related effects of cigarette smoking on olfactory function
-
Frye RE, Schwartz BS, Doty RL. 1990. Dose-related effects of cigarette smoking on olfactory function. JAMA. 263(9):1233-1236.
-
(1990)
JAMA
, vol.263
, Issue.9
, pp. 1233-1236
-
-
Frye, R.E.1
Schwartz, B.S.2
Doty, R.L.3
-
24
-
-
11144357919
-
Isolated congenital anosmia locus maps to 18p11.23-q12.2
-
Ghadami M, Morowati S, Majidzadeh-AK, Damavandi E, Nishimura G, Kinoshita A, Pasalar P, Komatsu K, Najafi MT, Niikawa N, et al. 2004. Isolated congenital anosmia locus maps to 18p11.23-q12.2. J Med Genet. 41(4):299-303.
-
(2004)
J Med Genet
, vol.41
, Issue.4
, pp. 299-303
-
-
Ghadami, M.1
Morowati, S.2
AK, M.3
Damavandi, E.4
Nishimura, G.5
Kinoshita, A.6
Pasalar, P.7
Komatsu, K.8
Najafi, M.T.9
Niikawa, N.10
-
25
-
-
0028828919
-
The genetic basis for specific anosmia to isovaleric acid in the mouse
-
Griff IC, Reed RR. 1995. The genetic basis for specific anosmia to isovaleric acid in the mouse: Cell. 83(3):407-414.
-
(1995)
Cell
, vol.83
, Issue.3
, pp. 407-414
-
-
Griff, I.C.1
Reed, R.R.2
-
26
-
-
0026766084
-
Evidence for genetic determination in human twins of olfactory thresholds for a standard odorant
-
Gross-Isseroff R, Ophir D, Bartana A, Voet H, Lancet D. 1992. Evidence for genetic determination in human twins of olfactory thresholds for a standard odorant Neurosci Lett. 141(1):115-118.
-
(1992)
Neurosci Lett
, vol.141
, Issue.1
, pp. 115-118
-
-
Gross-Isseroff, R.1
Ophir, D.2
Bartana, A.3
Voet, H.4
Lancet, D.5
-
27
-
-
0026701165
-
X chromosome-linked Kallmann syndrome: Stop mutations validate the candidate gene
-
Hardelin JP, Levilliers J, del Castillo I, Cohen-Salmon M, Legouis R, Blanchard S, Compain S, Bouloux P, Kirk J, Moraine C. et al. 1992. X chromosome-linked Kallmann syndrome: Stop mutations validate the candidate gene. Proc Natl Acad Sci USA. 89(17):8190-8194.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, Issue.17
, pp. 8190-8194
-
-
Hardelin, J.P.1
Levilliers, J.2
del Castillo, I.3
Cohen-Salmon, M.4
Legouis, R.5
Blanchard, S.6
Compain, S.7
Bouloux, P.8
Kirk, J.9
Moraine, C.10
-
28
-
-
0013952991
-
Hypogonadism and life-long anosmia
-
Hockaday TD. 1966. Hypogonadism and life-long anosmia. Postgrad Med J. 42(491):572-574.
-
(1966)
Postgrad Med J
, vol.42
, Issue.491
, pp. 572-574
-
-
Hockaday, T.D.1
-
29
-
-
0032451895
-
Age-related chhanges in the prevalence of smell/taste problems among the United States adult population. Results of the 1994 disability supplement to the National Health Interview Survey (NHIS)
-
Hoffman HJ, Ishii EK, MacTurk RH. 1998. Age-related chhanges in the prevalence of smell/taste problems among the United States adult population. Results of the 1994 disability supplement to the National Health Interview Survey (NHIS). Ann N Y Acad Sci. 855:716-722.
-
(1998)
Ann N Y Acad Sci
, vol.855
, pp. 716-722
-
-
Hoffman, H.J.1
Ishii, E.K.2
MacTurk, R.H.3
-
32
-
-
34848899273
-
Genetic variation in a human odorant receptor alters odour perception
-
Keller A, Zhuang H, Chi Q, Vosshall LB, Matsunami H. 2007. Genetic variation in a human odorant receptor alters odour perception. Nature. 446(7161):468-472.
-
(2007)
Nature
, vol.446
, Issue.7161
, pp. 468-472
-
-
Keller, A.1
Zhuang, H.2
Chi, Q.3
Vosshall, L.B.4
Matsunami, H.5
-
33
-
-
0842321051
-
Pathology of the olfactory mucosa: Implications for the treatment of olfactory dysfunction
-
Kern RC, Conley DB, Haines GK 3rd, Robinson AM. 2004. Pathology of the olfactory mucosa: Implications for the treatment of olfactory dysfunction. Laryngoscope. 114(2):279-285.
-
(2004)
Laryngoscope
, vol.114
, Issue.2
, pp. 279-285
-
-
Kern, R.C.1
Conley, D.B.2
Haines 3rd, G.K.3
Robinson, A.M.4
-
34
-
-
34247598905
-
Genetic component of identification, intensity and pleasantness of odours: A Finnish family study
-
Knaapila A, Keskitalo K, Kallela M, Wessman M, Sammalisto S, Hiekkalinna T, Palotie A, Peltonen L, Tuorila H, Perola M. 2007. Genetic component of identification, intensity and pleasantness of odours: A Finnish family study. Eur J Hum Genet. 15(5):596-602.
-
(2007)
Eur J Hum Genet
, vol.15
, Issue.5
, pp. 596-602
-
-
Knaapila, A.1
Keskitalo, K.2
Kallela, M.3
Wessman, M.4
Sammalisto, S.5
Hiekkalinna, T.6
Palotie, A.7
Peltonen, L.8
Tuorila, H.9
Perola, M.10
-
35
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA, Richardsson B, Sigurdardottir S, Barnard J, Hallbeck B, Masson G, et al. 2002. A high-resolution recombination map of the human genome. Nat Genet. 31(3):2411-247.
-
(2002)
Nat Genet
, vol.31
, Issue.3
, pp. 2411-3247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
-
36
-
-
0029886532
-
Parametric and non-parametric linkage analysis: A unified multipoint approach
-
Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. 1996. Parametric and non-parametric linkage analysis: A unified multipoint approach. Am J Hum Genet. 58(6):1347-1363.
-
(1996)
Am J Hum Genet
, vol.58
, Issue.6
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
37
-
-
4444254983
-
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse
-
Kulaga HM, Leitch CC, Eichers ER, Badano JL, Lesemann A, Hoskins BE, Lupski JR, Beales PL, Reed RR, Katsanis N. 2004. Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nat Genet. 36(9):994-998.
-
(2004)
Nat Genet
, vol.36
, Issue.9
, pp. 994-998
-
-
Kulaga, H.M.1
Leitch, C.C.2
Eichers, E.R.3
Badano, J.L.4
Lesemann, A.5
Hoskins, B.E.6
Lupski, J.R.7
Beales, P.L.8
Reed, R.R.9
Katsanis, N.10
-
38
-
-
23844435587
-
Sex differences in the genetic basis of morning serum cortisol levels: Genome-wide screen identifies two novel loci specific to women
-
Kurina LM, Weiss LA, Graves SW, Parry R, Williams GH, Abney M, Ober C. 2005. Sex differences in the genetic basis of morning serum cortisol levels: Genome-wide screen identifies two novel loci specific to women. J Clin Endocrinol Metab. 90(8):4747-4752.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, Issue.8
, pp. 4747-4752
-
-
Kurina, L.M.1
Weiss, L.A.2
Graves, S.W.3
Parry, R.4
Williams, G.H.5
Abney, M.6
Ober, C.7
-
39
-
-
33746572328
-
Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci
-
Kurz T, Hoffjan S, Hayes MG, Schneider D, Nicolae R, Heinzmann A, Jerkic SP, Parry R, Cox NJ, Deichmann KA, et al. 2006. Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci. J Allergy Clin Immunol. 118(2):396-402.
-
(2006)
J Allergy Clin Immunol
, vol.118
, Issue.2
, pp. 396-402
-
-
Kurz, T.1
Hoffjan, S.2
Hayes, M.G.3
Schneider, D.4
Nicolae, R.5
Heinzmann, A.6
Jerkic, S.P.7
Parry, R.8
Cox, N.J.9
Deichmann, K.A.10
-
40
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kiuglyak L. 1995. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 11(3):241-247.
-
(1995)
Nat Genet
, vol.11
, Issue.3
, pp. 241-247
-
-
Lander, E.1
Kiuglyak, L.2
-
41
-
-
0025940669
-
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
-
Legouis R, Hardelin JP, Levilliers J, Claverie JM, Compain S, Wunderle V, Millasseau P, Le Paslier D, Cohen D, Caterina D, et al. 1991. The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules. Cell. 67(2):423-435.
-
(1991)
Cell
, vol.67
, Issue.2
, pp. 423-435
-
-
Legouis, R.1
Hardelin, J.P.2
Levilliers, J.3
Claverie, J.M.4
Compain, S.5
Wunderle, V.6
Millasseau, P.7
Le Paslier, D.8
Cohen, D.9
Caterina, D.10
-
42
-
-
0035793042
-
Model-based analysis of oligonucleotide arrays: Expression index computation and outlier detection
-
Li C, Wong WH. 2001. Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection. Proc Nat Acad Sci USA. 98(1):31-36.
-
(2001)
Proc Nat Acad Sci USA
, vol.98
, Issue.1
, pp. 31-36
-
-
Li, C.1
Wong, W.H.2
-
43
-
-
0029610079
-
Performance on a smell screening test (the MODSIT): A study of 510 predominantly illiterate Chinese subjects
-
Liu HC, Wang SJ, Lin KP, Lin KN, Fuh JL, Teng EL. 1995. Performance on a smell screening test (the MODSIT): A study of 510 predominantly illiterate Chinese subjects. Physiol Behav. 58(6):1251-1255.
-
(1995)
Physiol Behav
, vol.58
, Issue.6
, pp. 1251-1255
-
-
Liu, H.C.1
Wang, S.J.2
Lin, K.P.3
Lin, K.N.4
Fuh, J.L.5
Teng, E.L.6
-
44
-
-
29444457877
-
Common deletion polymorphisms in the human genome
-
McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, et al. 2006. Common deletion polymorphisms in the human genome. Nat Genet. 38(1):86-92.
-
(2006)
Nat Genet
, vol.38
, Issue.1
, pp. 86-92
-
-
McCarroll, S.A.1
Hadnott, T.N.2
Perry, G.H.3
Sabeti, P.C.4
Zody, M.C.5
Barrett, J.C.6
Dallaire, S.7
Gabriel, S.B.8
Lee, C.9
Daly, M.J.10
-
45
-
-
84975864597
-
Population differences in haplotype structure within a human olfactory receptor gene cluster
-
Menashe I, Man O, Lancet D, Gilad Y. 2002, Population differences in haplotype structure within a human olfactory receptor gene cluster. Hum Mol Genet. 11(12):1381-1390.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.12
, pp. 1381-1390
-
-
Menashe, I.1
Man, O.2
Lancet, D.3
Gilad, Y.4
-
46
-
-
0038278868
-
Different noses for different people
-
Menashe I, Man O, Lancet D, Gilad Y. 2003. Different noses for different people. Nat Genet. 34(2):143-144.
-
(2003)
Nat Genet
, vol.34
, Issue.2
, pp. 143-144
-
-
Menashe, I.1
Man, O.2
Lancet, D.3
Gilad, Y.4
-
48
-
-
0037073289
-
Prevalence of olfactory impairment in older adults
-
Murphy C, Schubert CR, Cruickshanks KJ, Klein BE, Klein R, Nondahl DM. 2002. Prevalence of olfactory impairment in older adults. JAMA. 288(18):2307-2312.
-
(2002)
JAMA
, vol.288
, Issue.18
, pp. 2307-2312
-
-
Murphy, C.1
Schubert, C.R.2
Cruickshanks, K.J.3
Klein, B.E.4
Klein, R.5
Nondahl, D.M.6
-
49
-
-
0034967274
-
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4
-
Mykytyn K, Braun T, Carmi R, Haider NB, Searby CC, Shastri M, Beck G, Wright AF, Iannaccone A, Elbedour K, et al. 2001, Identification of the gene that, when mutated, causes the human obesity syndrome BBS4. Nat Genet. 28(2):188-191.
-
(2001)
Nat Genet
, vol.28
, Issue.2
, pp. 188-191
-
-
Mykytyn, K.1
Braun, T.2
Carmi, R.3
Haider, N.B.4
Searby, C.C.5
Shastri, M.6
Beck, G.7
Wright, A.F.8
Iannaccone, A.9
Elbedour, K.10
-
50
-
-
0036699538
-
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome
-
Mykytyn K, Nishimura DY, Searby CC, Shastri M, Yen HJ, Beck JS, Braun T, Streb LM, Cornier AS, Cox GF, et al. 2002. Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. Nat Genet. 31(4):435-438.
-
(2002)
Nat Genet
, vol.31
, Issue.4
, pp. 435-438
-
-
Mykytyn, K.1
Nishimura, D.Y.2
Searby, C.C.3
Shastri, M.4
Yen, H.J.5
Beck, J.S.6
Braun, T.7
Streb, L.M.8
Cornier, A.S.9
Cox, G.F.10
-
51
-
-
0037439542
-
Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree
-
Newman DL, Abney M, Dytch H, Parry R, McPeek MS, Ober C. 2003. Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree. Hum Mol Genet. 12(2):137-144.
-
(2003)
Hum Mol Genet
, vol.12
, Issue.2
, pp. 137-144
-
-
Newman, D.L.1
Abney, M.2
Dytch, H.3
Parry, R.4
McPeek, M.S.5
Ober, C.6
-
52
-
-
4043166989
-
Are common disease susceptibility alleles the same in outbred and founder populations?
-
Newman DL, Hoffjan S, Bourgain C, Abney M, Nicolae RI, Profits ET, Grow MA, Walker K, Steiner L, Parry R, et al. 2004. Are common disease susceptibility alleles the same in outbred and founder populations? Eur J Hum Genet. 12(7):584-590.
-
(2004)
Eur J Hum Genet
, vol.12
, Issue.7
, pp. 584-590
-
-
Newman, D.L.1
Hoffjan, S.2
Bourgain, C.3
Abney, M.4
Nicolae, R.I.5
Profits, E.T.6
Grow, M.A.7
Walker, K.8
Steiner, L.9
Parry, R.10
-
53
-
-
0035311942
-
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
-
Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, et al. 2001. Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2). Hum Mol Genet. 10(8):865-874.
-
(2001)
Hum Mol Genet
, vol.10
, Issue.8
, pp. 865-874
-
-
Nishimura, D.Y.1
Searby, C.C.2
Carmi, R.3
Elbedour, K.4
Van Maldergem, L.5
Fulton, A.B.6
Lam, B.L.7
Powell, B.R.8
Swiderski, R.E.9
Bugge, K.E.10
-
54
-
-
28144460266
-
Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene
-
Nishimura DY, Swiderski RE, Searby CC, Berg EM, Ferguson AL, Hennekam R, Merin S, Weleber RG, Biesecker LG, Stone EM et al. 2005. Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene. Am J Hum Genet. 77(6):1021-1033.
-
(2005)
Am J Hum Genet
, vol.77
, Issue.6
, pp. 1021-1033
-
-
Nishimura, D.Y.1
Swiderski, R.E.2
Searby, C.C.3
Berg, E.M.4
Ferguson, A.L.5
Hennekam, R.6
Merin, S.7
Weleber, R.G.8
Biesecker, L.G.9
Stone, E.M.10
-
55
-
-
0029059128
-
Unawareness of smell loss in normal aging and Alzheimer's disease: Discrepancy between self-reported and diagnosed smell sensitivity
-
Nordin S, Monsch AU, Murphy C. 1995. Unawareness of smell loss in normal aging and Alzheimer's disease: Discrepancy between self-reported and diagnosed smell sensitivity. J Gerontol B Psychol Sci Soc Sci. 50(4):P187-P192.
-
(1995)
J Gerontol B Psychol Sci Soc Sci
, vol.50
, Issue.4
-
-
Nordin, S.1
Monsch, A.U.2
Murphy, C.3
-
56
-
-
0034753277
-
The genetic dissection of complex traits in a founder population
-
Ober C, Abney M, McPeek MS. 2001. The genetic dissection of complex traits in a founder population. Am J Hum Genet. 69(5):1068-1079.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.5
, pp. 1068-1079
-
-
Ober, C.1
Abney, M.2
McPeek, M.S.3
-
57
-
-
0033431007
-
Genome-wide screen for atopy susceptibility alleles in the Hutterites
-
Ober C, Tsalenko A, Willadsen S, Newman D, Daniel R, Wu X, Andal J, Hoki D, Schneider D, True K. 1999. Genome-wide screen for atopy susceptibility alleles in the Hutterites. Clin Exp Allergy 29(Suppl 4):11-15.
-
(1999)
Clin Exp Allergy
, vol.29
, Issue.SUPPL. 4
, pp. 11-15
-
-
Ober, C.1
Tsalenko, A.2
Willadsen, S.3
Newman, D.4
Daniel, R.5
Wu, X.6
Andal, J.7
Hoki, D.8
Schneider, D.9
True, K.10
-
58
-
-
0033759713
-
A second-generation genomewide screen for asthma-susceptibility alleles in a founder population
-
Ober C, Tsalenko A, Parry R, Cox NJ. 2000. A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. Am J Hum Genet. 67(5):1154-1162.
-
(2000)
Am J Hum Genet
, vol.67
, Issue.5
, pp. 1154-1162
-
-
Ober, C.1
Tsalenko, A.2
Parry, R.3
Cox, N.J.4
-
59
-
-
33144470054
-
Comparison of subjective perception with objective measurement of olfaction
-
Philpott CM, Wolstenholme CR, Goodenough PC, Clark A, Murty GE. 2006. Comparison of subjective perception with objective measurement of olfaction. Otolaryngol Head Neck Surg. 134(3):488-490.
-
(2006)
Otolaryngol Head Neck Surg
, vol.134
, Issue.3
, pp. 488-490
-
-
Philpott, C.M.1
Wolstenholme, C.R.2
Goodenough, P.C.3
Clark, A.4
Murty, G.E.5
-
60
-
-
0034157649
-
Assessment of smell and taste in patients with allergic rhinitis
-
Rydzewski B, Pruszewicz A, Sulkowski WJ. 2000. Assessment of smell and taste in patients with allergic rhinitis. Acta Otolaryngol. 120(2):323-326.
-
(2000)
Acta Otolaryngol
, vol.120
, Issue.2
, pp. 323-326
-
-
Rydzewski, B.1
Pruszewicz, A.2
Sulkowski, W.J.3
-
61
-
-
0028872709
-
Twin analysis of odor identification and perception
-
Segal NL, Topolski TD, Wilson SM, Brown KW, Araki L. 1995. Twin analysis of odor identification and perception. Physiol Behav. 57(3):605-609.
-
(1995)
Physiol Behav
, vol.57
, Issue.3
, pp. 605-609
-
-
Segal, N.L.1
Topolski, T.D.2
Wilson, S.M.3
Brown, K.W.4
Araki, L.5
-
62
-
-
34249683710
-
Characterization of p43(ARF), a derivative of the p43 component of multi-aminoacyl-tRNA synthetase complex released during apoptosis
-
Shalak V, Guigou L, Kaminska M, Wautier MP, Wautier JL, Mirande M. 2007. Characterization of p43(ARF), a derivative of the p43 component of multi-aminoacyl-tRNA synthetase complex released during apoptosis. J Biol Chem. 282(15):10935-10943.
-
(2007)
J Biol Chem
, vol.282
, Issue.15
, pp. 10935-10943
-
-
Shalak, V.1
Guigou, L.2
Kaminska, M.3
Wautier, M.P.4
Wautier, J.L.5
Mirande, M.6
-
64
-
-
0031856129
-
Sense of smell in allergic and nonallergic rhinitis
-
Simola M, Malmberg H. 1998. Sense of smell in allergic and nonallergic rhinitis. Allergy. 53(2):190-194.
-
(1998)
Allergy
, vol.53
, Issue.2
, pp. 190-194
-
-
Simola, M.1
Malmberg, H.2
-
65
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K. 1996. Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet. 58(6):1323-1337.
-
(1996)
Am J Hum Genet
, vol.58
, Issue.6
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
66
-
-
33646354641
-
BBS10 encodes a vertebrate-spectric chaperonin-like protein and is a major BBS locus
-
Stoetzel C, Laurier V, Davis EE, Muller J, Rix S, Badano JL, Leitch CC, Salem N, Chouery E, Corbani S, et al. 2006. BBS10 encodes a vertebrate-spectric chaperonin-like protein and is a major BBS locus. Nat Genet. 38(5): 521-524.
-
(2006)
Nat Genet
, vol.38
, Issue.5
, pp. 521-524
-
-
Stoetzel, C.1
Laurier, V.2
Davis, E.E.3
Muller, J.4
Rix, S.5
Badano, J.L.6
Leitch, C.C.7
Salem, N.8
Chouery, E.9
Corbani, S.10
-
67
-
-
33845995129
-
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome
-
Stoetzel C, Muller J, Laurier V, Davis EE, Zaghloul NA, Vicaire S, Jacquelin C, Plewniak F, Leitch CC, Sarda P, et al. 2007. Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome. Am J Hum Genet 80(1):1-11.
-
(2007)
Am J Hum Genet
, vol.80
, Issue.1
, pp. 1-11
-
-
Stoetzel, C.1
Muller, J.2
Laurier, V.3
Davis, E.E.4
Zaghloul, N.A.5
Vicaire, S.6
Jacquelin, C.7
Plewniak, F.8
Leitch, C.C.9
Sarda, P.10
-
68
-
-
0036081317
-
Characteristics of olfactory disorders in relation to major causes of olfactory loss
-
Temmel AF, Quint C, Schickinger-Fischer B, Klimek L, Stoller E, Hummel T. 2002. Characteristics of olfactory disorders in relation to major causes of olfactory loss. Arch Otolaryngol Head Neck Surg. 128(6): 635-641.
-
(2002)
Arch Otolaryngol Head Neck Surg
, vol.128
, Issue.6
, pp. 635-641
-
-
Temmel, A.F.1
Quint, C.2
Schickinger-Fischer, B.3
Klimek, L.4
Stoller, E.5
Hummel, T.6
-
69
-
-
0037389629
-
The netrin-1 receptors UNC5H are putative tumor suppressors controlling cell death commitment
-
Thiebault K, Mazelin L, Pays L, Llambi F, Joly MO, Scoazec JY, Saurin JC, Romeo G, Mehlen P. 2003. The netrin-1 receptors UNC5H are putative tumor suppressors controlling cell death commitment. Proc. Natl Acad Sci USA. 100(7):4173-4178.
-
(2003)
Proc. Natl Acad Sci USA
, vol.100
, Issue.7
, pp. 4173-4178
-
-
Thiebault, K.1
Mazelin, L.2
Pays, L.3
Llambi, F.4
Joly, M.O.5
Scoazec, J.Y.6
Saurin, J.C.7
Romeo, G.8
Mehlen, P.9
-
70
-
-
21544458628
-
Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations
-
Weiss LA, Lester LA, Gern JE, Wolf RL, Parry R, Lemanske RF, Solway J, Ober C. 2005. Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations. Am J Respir Crit Care Med. 172(1): 67-73.
-
(2005)
Am J Respir Crit Care Med
, vol.172
, Issue.1
, pp. 67-73
-
-
Weiss, L.A.1
Lester, L.A.2
Gern, J.E.3
Wolf, R.L.4
Parry, R.5
Lemanske, R.F.6
Solway, J.7
Ober, C.8
-
71
-
-
31744449136
-
The sex-specific genetic architecture of quantitative traits in humans
-
Weiss LA, Pan L, Abney M, Ober C. 2006. The sex-specific genetic architecture of quantitative traits in humans. Nat Genet. 38(2):218-222.
-
(2006)
Nat Genet
, vol.38
, Issue.2
, pp. 218-222
-
-
Weiss, L.A.1
Pan, L.2
Abney, M.3
Ober, C.4
-
72
-
-
7744229124
-
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin
-
Weiss LA, Veenstra-Vanderweele J, Newman DL, Kim SJ, Dytch H, McPeek MS, Cheng S, Ober C, Cook EH Jr, Abney M. 2004. Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin. Eur J Hum Genet. 12(11):949-954.
-
(2004)
Eur J Hum Genet
, vol.12
, Issue.11
, pp. 949-954
-
-
Weiss, L.A.1
Veenstra-Vanderweele, J.2
Newman, D.L.3
Kim, S.J.4
Dytch, H.5
McPeek, M.S.6
Cheng, S.7
Ober, C.8
Cook Jr, E.H.9
Abney, M.10
-
73
-
-
0020554722
-
The syndrome of anosmia with hypogonadotropic hypogonadism: A genetic study of 18 new families and a review
-
White BJ, Rogol AD, Brown KS, Lieblich JM, Rosen SW 1983. The syndrome of anosmia with hypogonadotropic hypogonadism: A genetic study of 18 new families and a review. Am J Med Genet. 15(3):417-435.
-
(1983)
Am J Med Genet
, vol.15
, Issue.3
, pp. 417-435
-
-
White, B.J.1
Rogol, A.D.2
Brown, K.S.3
Lieblich, J.M.4
Rosen, S.W.5
-
74
-
-
33847171884
-
Genetic studies of stuttering in a founder population
-
Wittke-Thompson JK, Ambrose N, Yairi E, Roe C, Cook EH, Ober C, Cox NJ. 2006 Genetic studies of stuttering in a founder population. J Fluency Disord. 32(1):33-50.
-
(2006)
J Fluency Disord
, vol.32
, Issue.1
, pp. 33-50
-
-
Wittke-Thompson, J.K.1
Ambrose, N.2
Yairi, E.3
Roe, C.4
Cook, E.H.5
Ober, C.6
Cox, N.J.7
-
75
-
-
0032707163
-
Population choice in mapping genes for complex diseases
-
Wright AF, Carothers AD, Pirastu M. 1999. Population choice in mapping genes for complex diseases. Nat Genet. 23(4):397-404.
-
(1999)
Nat Genet
, vol.23
, Issue.4
, pp. 397-404
-
-
Wright, A.F.1
Carothers, A.D.2
Pirastu, M.3
-
76
-
-
0010791618
-
Ability to smell androstenone is genetically determined
-
Wysocki CJ, Beauchamp GK. 1984. Ability to smell androstenone is genetically determined. Proc Natl Acad Sci USA. 81(15):4899-4902.
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, Issue.15
, pp. 4899-4902
-
-
Wysocki, C.J.1
Beauchamp, G.K.2
-
77
-
-
0024319414
-
National Geographic smell survey. Effects of age are heterogenous
-
Wysocki CJ, Gilbert AN. 1989. National Geographic smell survey. Effects of age are heterogenous. Ann N Y Acad Sci. 561:12-28.
-
(1989)
Ann N Y Acad Sci
, vol.561
, pp. 12-28
-
-
Wysocki, C.J.1
Gilbert, A.N.2
-
78
-
-
0036163689
-
The olfactory receptor gene superfamily of the mouse
-
Zhang X, Firestein S. 2002. The olfactory receptor gene superfamily of the mouse. Nat Neurosci. 5(2):124-133.
-
(2002)
Nat Neurosci
, vol.5
, Issue.2
, pp. 124-133
-
-
Zhang, X.1
Firestein, S.2
|