-
1
-
-
0344691289
-
Genetics of sleep and sleep disorders
-
Franken, P. and Tafti, M. (2003) Genetics of sleep and sleep disorders. Frontiers Biosci. 8, e381-397.
-
(2003)
Frontiers Biosci
, vol.8
-
-
Franken, P.1
Tafti, M.2
-
2
-
-
14644392208
-
Genetics wakes up for human sleep
-
Lavie, P. (2005) Genetics wakes up for human sleep. Sleep Med. Rev. 9, 87-89.
-
(2005)
Sleep Med. Rev
, vol.9
, pp. 87-89
-
-
Lavie, P.1
-
3
-
-
20244380014
-
Orexins and orexin receptors: A family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior
-
Sakurai, T., Amemiya, A., Ishii, M., Matsuzaki, I., Chemelli, R. M., Tanaka, H., Williams, S. C., Richardson, J. A., Kozolwski, G. P., Wilson, S. et al. (1998) Orexins and orexin receptors: a family of hypothalamic neuropeptides and G protein-coupled receptors that regulate feeding behavior. Cell 92, 573-585.
-
(1998)
Cell
, vol.92
, pp. 573-585
-
-
Sakurai, T.1
Amemiya, A.2
Ishii, M.3
Matsuzaki, I.4
Chemelli, R.M.5
Tanaka, H.6
Williams, S.C.7
Richardson, J.A.8
Kozolwski, G.P.9
Wilson, S.10
-
4
-
-
0033588184
-
Narcolepsy in orexin knock-out mice:molecular genetics of sleep regulation
-
Chemelli, R. M., Willie, J. T., Sinton, C. M., Elmquist, J. K., Scammell, T., Lee, C., Richardson, J. A., Williams, S. C., Xiong, Y., Kisanuki, Y. et al. (1999) Narcolepsy in orexin knock-out mice:molecular genetics of sleep regulation. Cell 98, 437-451.
-
(1999)
Cell
, vol.98
, pp. 437-451
-
-
Chemelli, R.M.1
Willie, J.T.2
Sinton, C.M.3
Elmquist, J.K.4
Scammell, T.5
Lee, C.6
Richardson, J.A.7
Williams, S.C.8
Xiong, Y.9
Kisanuki, Y.10
-
5
-
-
0033529520
-
The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene
-
Lin, L., Faraco, J., Li, R., Kadotani, H., Rogers, W., Lin, X., Qui, X., de Jong, P. J., Nishino, S. and Mignot, E. (1999) The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene. Cell 98, 365-376.
-
(1999)
Cell
, vol.98
, pp. 365-376
-
-
Lin, L.1
Faraco, J.2
Li, R.3
Kadotani, H.4
Rogers, W.5
Lin, X.6
Qui, X.7
de Jong, P.J.8
Nishino, S.9
Mignot, E.10
-
6
-
-
0036606107
-
Sleep, feeding, and neuropeptides: Roles of orexins and orexin receptors
-
Mieda, M. and Yanagisawa, M. (2002) Sleep, feeding, and neuropeptides: roles of orexins and orexin receptors. Curr. Opin. Neurobiol. 12, 339-345.
-
(2002)
Curr. Opin. Neurobiol
, vol.12
, pp. 339-345
-
-
Mieda, M.1
Yanagisawa, M.2
-
7
-
-
0036580756
-
The hypocretins: Setting the arousal threshold
-
Sutcliffe, J. G. and de Lecea, L. (2002) The hypocretins: setting the arousal threshold. Nat. Rev. 3, 339-349.
-
(2002)
Nat. Rev
, vol.3
, pp. 339-349
-
-
Sutcliffe, J.G.1
de Lecea, L.2
-
8
-
-
22144479803
-
Roles of orexin/hypocretin in regulation of sleep/wakefulness and energy homeostasis
-
Sakurai, T. (2005) Roles of orexin/hypocretin in regulation of sleep/wakefulness and energy homeostasis. Sleep Med. Rev. 9, 231-241.
-
(2005)
Sleep Med. Rev
, vol.9
, pp. 231-241
-
-
Sakurai, T.1
-
9
-
-
0033826856
-
Amutation in early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
-
Peyron, C., Faraco, J., Rogers, W., Ripley, B., Overeem, S., Charnay, Y., Nevsimalova, S., Aldrich, M., Reynolds, D., Albin, R. et al. (2000)Amutation in early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nat. Med. 6, 991-997.
-
(2000)
Nat. Med
, vol.6
, pp. 991-997
-
-
Peyron, C.1
Faraco, J.2
Rogers, W.3
Ripley, B.4
Overeem, S.5
Charnay, Y.6
Nevsimalova, S.7
Aldrich, M.8
Reynolds, D.9
Albin, R.10
-
10
-
-
0012110908
-
The genetics of sleep disorders
-
Taheri, S. and Mignot, E. (2002)The genetics of sleep disorders. Lancet Neurol. 1, 242-250.
-
(2002)
Lancet Neurol
, vol.1
, pp. 242-250
-
-
Taheri, S.1
Mignot, E.2
-
11
-
-
14644408095
-
Genetics of normal and pathological sleep in humans
-
Dauvilliers, Y., Maret, S. and Tafti, M. (2005) Genetics of normal and pathological sleep in humans. Sleep Med. Rev. 9, 91-100.
-
(2005)
Sleep Med. Rev
, vol.9
, pp. 91-100
-
-
Dauvilliers, Y.1
Maret, S.2
Tafti, M.3
-
12
-
-
0033057814
-
EEG patterns in twins
-
Linkowski, P. (1999) EEG patterns in twins. J. Sleep Res. 8 (suppl 1), 11-13.
-
(1999)
J. Sleep Res
, vol.8
, Issue.SUPPL. 1
, pp. 11-13
-
-
Linkowski, P.1
-
13
-
-
0020503776
-
Relationships in sleep characteristics of identical and fraternal twins
-
Webb, W. B. and Campbell, S. S. (1983) Relationships in sleep characteristics of identical and fraternal twins. Arch. Gen. Psychiat. 40, 1093-1095.
-
(1983)
Arch. Gen. Psychiat
, vol.40
, pp. 1093-1095
-
-
Webb, W.B.1
Campbell, S.S.2
-
14
-
-
0025184217
-
Evidence for genetic influences on sleep disturbance and sleep pattern in twins
-
Heath, A. C., Kendler, K. S., Eaves, L. J. and Martin, N. G. (1990) Evidence for genetic influences on sleep disturbance and sleep pattern in twins. Sleep 13, 318-335.
-
(1990)
Sleep
, vol.13
, pp. 318-335
-
-
Heath, A.C.1
Kendler, K.S.2
Eaves, L.J.3
Martin, N.G.4
-
15
-
-
0020629497
-
Genetic and environmental determination of human sleep
-
Partinen, M., Kaprio, J., Koskenvuo, M., Putkonen, P. and Langinvainio, H. (1983) Genetic and environmental determination of human sleep. Sleep 6, 179-185.
-
(1983)
Sleep
, vol.6
, pp. 179-185
-
-
Partinen, M.1
Kaprio, J.2
Koskenvuo, M.3
Putkonen, P.4
Langinvainio, H.5
-
16
-
-
0036773740
-
Twin and family studies of the human electroencephalogram: A review and a meta-analysis
-
Van Beijsterveldt, C. E. M. and van Baal, G. C. M. (2002) Twin and family studies of the human electroencephalogram: a review and a meta-analysis. Biol. Psychiat. 61, 111-138.
-
(2002)
Biol. Psychiat
, vol.61
, pp. 111-138
-
-
Van Beijsterveldt, C.E.M.1
van Baal, G.C.M.2
-
17
-
-
0001383694
-
Action potentials of the brain in normal persons and in normal states of cerebral activity
-
Davis, H. and Davis, P. (1936) Action potentials of the brain in normal persons and in normal states of cerebral activity. Arch. Neurol. Psychiat. 36, 1214-1224.
-
(1936)
Arch. Neurol. Psychiat
, vol.36
, pp. 1214-1224
-
-
Davis, H.1
Davis, P.2
-
18
-
-
77957217441
-
The brain-wave patterns and hereditary trait
-
Lennox, W., Gibbs, E. and Gibbs, F. (1945) The brain-wave patterns and hereditary trait. J. Heredity 36, 233-243.
-
(1945)
J. Heredity
, vol.36
, pp. 233-243
-
-
Lennox, W.1
Gibbs, E.2
Gibbs, F.3
-
19
-
-
34249021642
-
Sleep architecture and sleep continuity in healthy twins
-
Friess, E., Ambrosius, U., Lietzenmayer, S., Wichniak, A., Winkelmann, J., Yassouridis, A. and Holsboer, F. (2005) Sleep architecture and sleep continuity in healthy twins. Pharmacopsychiatry 38, 241-242.
-
(2005)
Pharmacopsychiatry
, vol.38
, pp. 241-242
-
-
Friess, E.1
Ambrosius, U.2
Lietzenmayer, S.3
Wichniak, A.4
Winkelmann, J.5
Yassouridis, A.6
Holsboer, F.7
-
20
-
-
0035997179
-
The influence of heredity on self-reported sleep patterns in free-living humans
-
De Castro, J. M. (2002) The influence of heredity on self-reported sleep patterns in free-living humans. Physiol. Behav. 76, 479-486.
-
(2002)
Physiol. Behav
, vol.76
, pp. 479-486
-
-
De Castro, J.M.1
-
21
-
-
0007051350
-
Familial incidence of insomnia
-
Bastien, C. H. and Morin, C. M. (2000) Familial incidence of insomnia. J. Sleep Res. 9, 49-54.
-
(2000)
J. Sleep Res
, vol.9
, pp. 49-54
-
-
Bastien, C.H.1
Morin, C.M.2
-
22
-
-
0036753006
-
The Munich vulnerability study on affective disorders: Stability of polysomnographic findings over time
-
Modell, S., Ising, M., Holsboer, F. and Lauer, C. J. (2002) The Munich vulnerability study on affective disorders: stability of polysomnographic findings over time. Biol. Psychiat. 52, 430-437.
-
(2002)
Biol. Psychiat
, vol.52
, pp. 430-437
-
-
Modell, S.1
Ising, M.2
Holsboer, F.3
Lauer, C.J.4
-
23
-
-
0024467138
-
EEG sleep paterns in man: A twin study
-
Linkowski, P., Kerkhofs, M., Hauspie, R., Susanne, C. and Mendlewicz, J. (1989) EEG sleep paterns in man: a twin study. Electroencephalogr. Clin. Neurophysiol. 73, 279-284.
-
(1989)
Electroencephalogr. Clin. Neurophysiol
, vol.73
, pp. 279-284
-
-
Linkowski, P.1
Kerkhofs, M.2
Hauspie, R.3
Susanne, C.4
Mendlewicz, J.5
-
24
-
-
0025767797
-
Genetic determinations of EEG sleep: A study in twins living apart
-
Linkowski, P., Kerkhofs, M., Hauspie, R. and Mendlewicz, J. (1991) Genetic determinations of EEG sleep: a study in twins living apart. Electroencephalogr. Clin. Neurophysiol. 79, 114-118.
-
(1991)
Electroencephalogr. Clin. Neurophysiol
, vol.79
, pp. 114-118
-
-
Linkowski, P.1
Kerkhofs, M.2
Hauspie, R.3
Mendlewicz, J.4
-
25
-
-
0030029838
-
Heritability of human brain functioning as assessed by electroencephalography
-
Van Beijsterveldt, C. E. M., Molenaar, P. C. M., de Geus, E. J. C. and Boomsma, D. I. (1996) Heritability of human brain functioning as assessed by electroencephalography. Am. J. Hum. Genet. 58, 562-573.
-
(1996)
Am. J. Hum. Genet
, vol.58
, pp. 562-573
-
-
Van Beijsterveldt, C.E.M.1
Molenaar, P.C.M.2
de Geus, E.J.C.3
Boomsma, D.I.4
-
26
-
-
0014953006
-
The genetic basis of the normal human electroencephalogram (EEG)
-
Vogel, F. (1970) The genetic basis of the normal human electroencephalogram (EEG). Humangenetik 10, 91-114.
-
(1970)
Humangenetik
, vol.10
, pp. 91-114
-
-
Vogel, F.1
-
27
-
-
0026553008
-
Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity
-
Steinlein, O., Anokhin, A., Yping, M., Schalt, E. and Vogel, F. (1992) Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity. Genomics 12, 69-73.
-
(1992)
Genomics
, vol.12
, pp. 69-73
-
-
Steinlein, O.1
Anokhin, A.2
Yping, M.3
Schalt, E.4
Vogel, F.5
-
28
-
-
27344454837
-
A function genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans
-
Ŕetey, J. V., Adam, M., Honegger, E., Khatami, R., Luhmann, U. F. O., Jung, H. H., Berger, W. and Landolt, H.-P. (2005) A function genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans. PNAS 102, 15676-15681.
-
(2005)
PNAS
, vol.102
, pp. 15676-15681
-
-
Ŕetey, J.V.1
Adam, M.2
Honegger, E.3
Khatami, R.4
Luhmann, U.F.O.5
Jung, H.H.6
Berger, W.7
Landolt, H.-P.8
-
29
-
-
0026496257
-
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Desease phenotype determined by a DNA polymorphism
-
Goldfarb, L. G., Petersen, R. B., Tabaton, M., Brawn, P., LeBlanc, A. C., Montagna, P., Cortelli, P., Julien, J., Vital, C., Pendelbury, W. W. et al. (1992) Fatal familial insomnia and familial Creutzfeldt-Jakob disease: desease phenotype determined by a DNA polymorphism. Science 258, 806-808.
-
(1992)
Science
, vol.258
, pp. 806-808
-
-
Goldfarb, L.G.1
Petersen, R.B.2
Tabaton, M.3
Brawn, P.4
LeBlanc, A.C.5
Montagna, P.6
Cortelli, P.7
Julien, J.8
Vital, C.9
Pendelbury, W.W.10
-
30
-
-
7144253795
-
Clinical features of Fetal Familial Insomnia: Phenotypic variability in relation to a polymorphism at codon 129 of the prion protein
-
Montagna, P., Cortelli, P., Avoni, P., Tinuper, P., Plazzi, G., Gallassi, R., Portaluppi, F., Julien, J., Vital, C., Delisle, M. B. et al. (1998) Clinical features of Fetal Familial Insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein. Brain Pathol. 8, 515-520.
-
(1998)
Brain Pathol
, vol.8
, pp. 515-520
-
-
Montagna, P.1
Cortelli, P.2
Avoni, P.3
Tinuper, P.4
Plazzi, G.5
Gallassi, R.6
Portaluppi, F.7
Julien, J.8
Vital, C.9
Delisle, M.B.10
-
31
-
-
0036460292
-
Effect of the prion 129 polymorphism on nocturnal sleep and insomnia complaints: A population-base study
-
Pedrazzoli, M., Ling, L., Young, T. B., Finn, L., Tufik, S. and Mignot, E. (2002) Effect of the prion 129 polymorphism on nocturnal sleep and insomnia complaints: a population-base study. J. Sleep Res. 11, 357-358.
-
(2002)
J. Sleep Res
, vol.11
, pp. 357-358
-
-
Pedrazzoli, M.1
Ling, L.2
Young, T.B.3
Finn, L.4
Tufik, S.5
Mignot, E.6
-
32
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
Tobler, I., Gaus, S. E., Deboer, T., Achermann, P., Fischer, M., Rlicke, T., Moser, M., Ocesch, B., McBride, P. A. and Manson, J. C. (1996) Altered circadian activity rhythms and sleep in mice devoid of prion protein. Nature 380, 639-642.
-
(1996)
Nature
, vol.380
, pp. 639-642
-
-
Tobler, I.1
Gaus, S.E.2
Deboer, T.3
Achermann, P.4
Fischer, M.5
Rlicke, T.6
Moser, M.7
Ocesch, B.8
McBride, P.A.9
Manson, J.C.10
-
33
-
-
0030822582
-
Prion diseases and the BSE crisis
-
Prusiner, A. B. (1997) Prion diseases and the BSE crisis. Science 278, 245-251.
-
(1997)
Science
, vol.278
, pp. 245-251
-
-
Prusiner, A.B.1
-
34
-
-
0023402101
-
EEG power density during nap sleep: Reflection of an hourglass measuring the duration of prior wakefulness
-
Dijk, D. J., Beersma, D. G. and Daan, S. (1987) EEG power density during nap sleep: reflection of an hourglass measuring the duration of prior wakefulness. J. Biol. Rhythms 2, 207-219.
-
(1987)
J. Biol. Rhythms
, vol.2
, pp. 207-219
-
-
Dijk, D.J.1
Beersma, D.G.2
Daan, S.3
-
36
-
-
0033047074
-
Prion protein: A role in sleep regulation?
-
Huber, R., Deboer, T. and Tobler, I. (1999) Prion protein: a role in sleep regulation? J. Sleep Res. 8 (Suppl 1), 30-36.
-
(1999)
J. Sleep Res
, vol.8
, Issue.SUPPL. 1
, pp. 30-36
-
-
Huber, R.1
Deboer, T.2
Tobler, I.3
-
37
-
-
0016373716
-
A diallel analysis of the genetic underpinnings of mouse sleep
-
Friedmann, J. K. (1974) A diallel analysis of the genetic underpinnings of mouse sleep. Physiol. Behav. 12, 169-175.
-
(1974)
Physiol. Behav
, vol.12
, pp. 169-175
-
-
Friedmann, J.K.1
-
38
-
-
0015527219
-
Genetic studies of sleep in mice
-
Valatx, J. L., Bugat, R. and Jouvet, M. (1972) Genetic studies of sleep in mice. Nature 238, 226-227.
-
(1972)
Nature
, vol.238
, pp. 226-227
-
-
Valatx, J.L.1
Bugat, R.2
Jouvet, M.3
-
39
-
-
0031738539
-
-
Franken, P., Malafosse, A. and Tafti, M. (1998) Genetic variation in EEG activity during sleep in inbred mice. Am. J. Physiol. Reg. Inteq. Comp. Physiol. 275, R1127-R1137. http://ajpregu.physiology.org/.
-
Franken, P., Malafosse, A. and Tafti, M. (1998) Genetic variation in EEG activity during sleep in inbred mice. Am. J. Physiol. Reg. Inteq. Comp. Physiol. 275, R1127-R1137. http://ajpregu.physiology.org/.
-
-
-
-
40
-
-
0038757817
-
Deficiency in shortchain fatty acid β-oxidation affects theta oscillations during sleep
-
Tafti, M., Petit, B., Chollet, D., Neidhart, E., deBilbao, F., Kiss, J. Z., Wood, P. A. and Franken, P. (2003) Deficiency in shortchain fatty acid β-oxidation affects theta oscillations during sleep. Nat. Genet. 34, 320-325.
-
(2003)
Nat. Genet
, vol.34
, pp. 320-325
-
-
Tafti, M.1
Petit, B.2
Chollet, D.3
Neidhart, E.4
deBilbao, F.5
Kiss, J.Z.6
Wood, P.A.7
Franken, P.8
-
41
-
-
0033559893
-
Genetic determinants of sleep regulation in inbred mice
-
Franken, P., Malafosse, A. and Tafti, M. (1999) Genetic determinants of sleep regulation in inbred mice. Sleep 22, 155-169.
-
(1999)
Sleep
, vol.22
, pp. 155-169
-
-
Franken, P.1
Malafosse, A.2
Tafti, M.3
-
42
-
-
0035871645
-
The homeostatic regulation of sleep need is under genetic control
-
Franken, P., Chollet, D. and Tafti, M. (2001) The homeostatic regulation of sleep need is under genetic control. J. Neurosci. 21, 2610-2621.
-
(2001)
J. Neurosci
, vol.21
, pp. 2610-2621
-
-
Franken, P.1
Chollet, D.2
Tafti, M.3
-
43
-
-
0031468568
-
Localization of candidate genomic regions influencing paradoxical sleep in mice
-
Tafti, M., Franken, P., Kitahama, K., Malafosse, A., Jouvet, M. and Valatx, J. L. (1997) Localization of candidate genomic regions influencing paradoxical sleep in mice. Neuroreport 8, 3755-3758.
-
(1997)
Neuroreport
, vol.8
, pp. 3755-3758
-
-
Tafti, M.1
Franken, P.2
Kitahama, K.3
Malafosse, A.4
Jouvet, M.5
Valatx, J.L.6
-
44
-
-
0347885320
-
A role for cryptochromes in sleep regulation
-
Wisor, J. P., O'Hara, B. F., Terao, A., Selby, C. P., Kilduff, T. S., Sancar, A., Edgar, D. M. and Franken, P. (2002) A role for cryptochromes in sleep regulation. BMC Neurosci. 3, 20.
-
(2002)
BMC Neurosci
, vol.3
, pp. 20
-
-
Wisor, J.P.1
O'Hara, B.F.2
Terao, A.3
Selby, C.P.4
Kilduff, T.S.5
Sancar, A.6
Edgar, D.M.7
Franken, P.8
-
45
-
-
0038454431
-
Altered patterns of sleep and behavioral adaptability in NPAS2-deficient mice
-
Dudley, C. A., Erbel-Sieler, C., Estill, S. J., Reick, M., Franken, P., Pitts, S. and McKnight, S. L. (2003) Altered patterns of sleep and behavioral adaptability in NPAS2-deficient mice. Science 301, 379-383.
-
(2003)
Science
, vol.301
, pp. 379-383
-
-
Dudley, C.A.1
Erbel-Sieler, C.2
Estill, S.J.3
Reick, M.4
Franken, P.5
Pitts, S.6
McKnight, S.L.7
-
46
-
-
33646472265
-
NPAS2 as a transcriptional regulator of non-rapid eye movement sleep: Genotype and sex interactions
-
Franken, P., Dudley, C. A., Estill, S. J., Barakat, M., Thomason, R., O'Hara, B. and McKnight, S. L. (2006) NPAS2 as a transcriptional regulator of non-rapid eye movement sleep: Genotype and sex interactions. PNAS 103, 7118-7123.
-
(2006)
PNAS
, vol.103
, pp. 7118-7123
-
-
Franken, P.1
Dudley, C.A.2
Estill, S.J.3
Barakat, M.4
Thomason, R.5
O'Hara, B.6
McKnight, S.L.7
-
47
-
-
11144221996
-
G-subunit of T-type calcium channels
-
G-subunit of T-type calcium channels. PNAS 101, 18195-18199.
-
(2004)
PNAS
, vol.101
, pp. 18195-18199
-
-
Lee, J.1
Kim, D.2
Shin, H.-S.3
-
48
-
-
0034879821
-
2+ channels
-
2+ channels. Neuron 31, 35-45.
-
(2001)
Neuron
, vol.31
, pp. 35-45
-
-
Kim, D.1
Song, I.2
Keum, S.3
Lee, T.4
Jeong, M.-J.5
Kim, S.-S.6
McEnery, M.W.7
Shin, H.S.8
-
49
-
-
34249017876
-
Site-specific CRH overexpression alters sleep in transgenic mice
-
Kimura, M., Müller-Preuss, P., Wiesner, E., Lu, A. and Deussing, J. M. (2006) Site-specific CRH overexpression alters sleep in transgenic mice. J. Sleep Res. 15 (suppl. 1), 101.
-
(2006)
J. Sleep Res
, vol.15
, Issue.SUPPL. 1
, pp. 101
-
-
Kimura, M.1
Müller-Preuss, P.2
Wiesner, E.3
Lu, A.4
Deussing, J.M.5
-
50
-
-
0034782625
-
Modulation of brain gene expression during sleep and wakefulness: A review of recent findings
-
Tononi, G. and Cirelli, C. (2001) Modulation of brain gene expression during sleep and wakefulness: a review of recent findings. Neuropsychopharmacology 25, S28-S35.
-
(2001)
Neuropsychopharmacology
, vol.25
-
-
Tononi, G.1
Cirelli, C.2
-
51
-
-
0034624293
-
Gene expression in the brain across the sleep-waking cycle
-
Cirelli, C. and Tononi, G. (2000) Gene expression in the brain across the sleep-waking cycle. Brain Res. 885, 303-321.
-
(2000)
Brain Res
, vol.885
, pp. 303-321
-
-
Cirelli, C.1
Tononi, G.2
-
52
-
-
24144498431
-
Sleep and wakefulness modulate gene expression in Drosophila
-
Cirelli, C., LaVaute, T. M. and Tononi, G. (2005) Sleep and wakefulness modulate gene expression in Drosophila. J. Neurochem. 94, 1411-1419.
-
(2005)
J. Neurochem
, vol.94
, pp. 1411-1419
-
-
Cirelli, C.1
LaVaute, T.M.2
Tononi, G.3
-
53
-
-
0347948474
-
Extensive and divergent effects of sleep and wakefulness on brain gene expression
-
Cirelli, C., Gutierrez, C. and Tononi, G.. (2004) Extensive and divergent effects of sleep and wakefulness on brain gene expression. Neuron 41, 35-43.
-
(2004)
Neuron
, vol.41
, pp. 35-43
-
-
Cirelli, C.1
Gutierrez, C.2
Tononi, G.3
-
54
-
-
0037439241
-
Differentially increase in the expression of heat shock protein family members during sleep deprivation and during sleep
-
Terao, A., Steininger, T. L., Hyder, K., Apte-Deshpande, A., Ding, J., Rishipathak, D., Davis, R. W., Heller, H. C. and Kilduff, T. S. (2003) Differentially increase in the expression of heat shock protein family members during sleep deprivation and during sleep. Neuroscience 116, 187-200.
-
(2003)
Neuroscience
, vol.116
, pp. 187-200
-
-
Terao, A.1
Steininger, T.L.2
Hyder, K.3
Apte-Deshpande, A.4
Ding, J.5
Rishipathak, D.6
Davis, R.W.7
Heller, H.C.8
Kilduff, T.S.9
-
55
-
-
0034967563
-
Comparison of global brain gene expression profiles between inbred long-sleep and inbred short-sleep mice by high-density gene array hybridization
-
Xu, Y., Ehringer, M., Yang, F. and Sikela, J. M. (2001) Comparison of global brain gene expression profiles between inbred long-sleep and inbred short-sleep mice by high-density gene array hybridization. Alcohol Clin. Exp. Res. 25, 810-818.
-
(2001)
Alcohol Clin. Exp. Res
, vol.25
, pp. 810-818
-
-
Xu, Y.1
Ehringer, M.2
Yang, F.3
Sikela, J.M.4
-
56
-
-
0036250002
-
Are there ethnic differences in sleep architecture?
-
Profant, J., Ancoli-Israel, S. and Dimsdale, J. E. (2002) Are there ethnic differences in sleep architecture? Am. J. Human Biol. 14, 321-326.
-
(2002)
Am. J. Human Biol
, vol.14
, pp. 321-326
-
-
Profant, J.1
Ancoli-Israel, S.2
Dimsdale, J.E.3
-
57
-
-
0041851052
-
Effect of ethnicity on sleep: Complexities for epidemiologic research
-
Stepnowsky, C. J., Moore, P. J. and Dimsdale, J. E. (2003) Effect of ethnicity on sleep: complexities for epidemiologic research. Sleep 26, 329-332.
-
(2003)
Sleep
, vol.26
, pp. 329-332
-
-
Stepnowsky, C.J.1
Moore, P.J.2
Dimsdale, J.E.3
-
58
-
-
0037738587
-
Restless legs syndrome: Diagnostic criteria, special considerations, and epidemiology. A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health
-
Allen, R. P., Picchietti, D., Hening, W. A., Trenkwalder, C., Walters, A. S. and Montplaisi, J. (2003) Restless legs syndrome: diagnostic criteria, special considerations, and epidemiology. A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health. Sleep Med. 4, 101-119.
-
(2003)
Sleep Med
, vol.4
, pp. 101-119
-
-
Allen, R.P.1
Picchietti, D.2
Hening, W.A.3
Trenkwalder, C.4
Walters, A.S.5
Montplaisi, J.6
-
59
-
-
0034255111
-
Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients
-
Winkelmann, J., Wetter, T. C., Collado-Seidel, V., Gasser, T., Dichgans, M., Yassouridis, A. and Trenkwalder, C. (2000) Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients. Sleep 23, 597-602.
-
(2000)
Sleep
, vol.23
, pp. 597-602
-
-
Winkelmann, J.1
Wetter, T.C.2
Collado-Seidel, V.3
Gasser, T.4
Dichgans, M.5
Yassouridis, A.6
Trenkwalder, C.7
-
60
-
-
0029730801
-
Restless legs syndrome: Clinicoetiologic correlates
-
Ondo, W. G. and Jankovic, J. (1996) Restless legs syndrome: clinicoetiologic correlates. Neurology 47, 1435-1441.
-
(1996)
Neurology
, vol.47
, pp. 1435-1441
-
-
Ondo, W.G.1
Jankovic, J.2
-
61
-
-
0031027378
-
Clinical, polysomnographic, and genetic characteristics of restless legs syndrome: A study of 133 patients diagnosed with new standard criteria
-
Montplaisir, J., Boucher, S., Priorier, G., Lavigne, G., Lapierre, O. and Lesperance, P. (1997) Clinical, polysomnographic, and genetic characteristics of restless legs syndrome: a study of 133 patients diagnosed with new standard criteria. Mov. Disord. 12, 61-65.
-
(1997)
Mov. Disord
, vol.12
, pp. 61-65
-
-
Montplaisir, J.1
Boucher, S.2
Priorier, G.3
Lavigne, G.4
Lapierre, O.5
Lesperance, P.6
-
62
-
-
0034649387
-
Restless legs syndrome in monocygotic twins: Clinical correlates
-
Ondo, W. G., Vuong, K. V. and Wang, Q. (2000) Restless legs syndrome in monocygotic twins: clinical correlates. Neurology 55, 1404-1406.
-
(2000)
Neurology
, vol.55
, pp. 1404-1406
-
-
Ondo, W.G.1
Vuong, K.V.2
Wang, Q.3
-
63
-
-
0036714378
-
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families
-
Winkelmann, J., Müller-Myhsok, B., Wittchen, H. U., Hock, B., Prager, M., Pfister, H., Strhole, A., Eisensehr, I., Dichgans, M., Gasser, T. and Trenkwalder, C. (2002) Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families. Ann. Neurol. 52, 297-302.
-
(2002)
Ann. Neurol
, vol.52
, pp. 297-302
-
-
Winkelmann, J.1
Müller-Myhsok, B.2
Wittchen, H.U.3
Hock, B.4
Prager, M.5
Pfister, H.6
Strhole, A.7
Eisensehr, I.8
Dichgans, M.9
Gasser, T.10
Trenkwalder, C.11
-
64
-
-
0035208888
-
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q
-
Desautels, A., Turecki, G., Montplaisir, J., Sequeira, A., Verner, A. and Rouleau, G. A. (2001) Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q. Am. J. Hum. Genet. 69, 1266-1270.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 1266-1270
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Sequeira, A.4
Verner, A.5
Rouleau, G.A.6
-
65
-
-
20144387708
-
Restless legs syndrome: Confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity
-
Desautels, A., Turecki, G., Montplaisir, J., Xiong, L., Walters, A. S., Ehrenberg, B. L., Brisebois K, Desautels, A. K., Gingras, Y., Johnson, W. G.. et al. (2005) Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity. Arch. Neurol. 62, 591-596.
-
(2005)
Arch. Neurol
, vol.62
, pp. 591-596
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Xiong, L.4
Walters, A.S.5
Ehrenberg, B.L.6
Brisebois, K.7
Desautels, A.K.8
Gingras, Y.9
Johnson, W.G.10
-
66
-
-
0038691989
-
Autosomal dominant restless legs syndrome maps on chromosome 14q
-
Bonati, M. T., Ferini-Strambi, L., Aridon, P., Oldani, A., Zucconi, M. and Casari, G. (2003) Autosomal dominant restless legs syndrome maps on chromosome 14q. Brain 126, 1485-1492.
-
(2003)
Brain
, vol.126
, pp. 1485-1492
-
-
Bonati, M.T.1
Ferini-Strambi, L.2
Aridon, P.3
Oldani, A.4
Zucconi, M.5
Casari, G.6
-
67
-
-
2542595563
-
The 14q restless legs syndrome locus in the French Canadian population
-
Levchenko, A., Montplaisir, J. Y., Dube, M. P., Riviere, J. B., St-Onge, J., Turecki, G., Xiong, L., Thibodeau, P., Desautels, A., Verlaan, D. J. and Rouleau, G. A. (2004) The 14q restless legs syndrome locus in the French Canadian population. Ann. Neurol. 55, 887-891.
-
(2004)
Ann. Neurol
, vol.55
, pp. 887-891
-
-
Levchenko, A.1
Montplaisir, J.Y.2
Dube, M.P.3
Riviere, J.B.4
St-Onge, J.5
Turecki, G.6
Xiong, L.7
Thibodeau, P.8
Desautels, A.9
Verlaan, D.J.10
Rouleau, G.A.11
-
68
-
-
2342527865
-
Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p
-
Chen, S., Ondo, W. G., Rao, S., Li, L., Chen, Q. and Wang, Q. (2004) Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p. Am. J. Hum. Genet. 74, 876-885.
-
(2004)
Am. J. Hum. Genet
, vol.74
, pp. 876-885
-
-
Chen, S.1
Ondo, W.G.2
Rao, S.3
Li, L.4
Chen, Q.5
Wang, Q.6
-
69
-
-
15944376234
-
No convincing evidence of linkage for restless legs syndrome on chromosome 9p
-
Ray, A. and Weeks, D. E. (2005) No convincing evidence of linkage for restless legs syndrome on chromosome 9p. Am. J. Hum. Genet. 76, 705-707.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 705-707
-
-
Ray, A.1
Weeks, D.E.2
-
70
-
-
33747037830
-
Restless Legs Syndrome-3: Fine-mapping in a family with intrafamilial heterogeneity
-
Liebetanz, K. M., Winkelmann, J., Trenkwalder, C., Pütz, B., Dichgans, M., Gasser, T. and Müller-Myhsok, B. (2006) Restless Legs Syndrome-3: fine-mapping in a family with intrafamilial heterogeneity. Neurology 67, 320-321.
-
(2006)
Neurology
, vol.67
, pp. 320-321
-
-
Liebetanz, K.M.1
Winkelmann, J.2
Trenkwalder, C.3
Pütz, B.4
Dichgans, M.5
Gasser, T.6
Müller-Myhsok, B.7
-
71
-
-
0035833952
-
Dopaminergic neurotransmission and restless legs syndrome: A genetic association analysis
-
Desautels, A., Turecki, G., Montplaisir, J., Ftouhi-Paquin, N., Michaud, M., Chouinard, V. A. and Rouleau, G. A. (2001) Dopaminergic neurotransmission and restless legs syndrome: a genetic association analysis. Neurology 57, 1304-1306.
-
(2001)
Neurology
, vol.57
, pp. 1304-1306
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Ftouhi-Paquin, N.4
Michaud, M.5
Chouinard, V.A.6
Rouleau, G.A.7
-
72
-
-
0037162352
-
Evidence for a genetic association between monoamine oxidase A and restless legs syndrome
-
Desautels, A., Turecki, G., Montplaisir, J., Brisebois, K., Sequeira, A., Adam, B. and Rouleau, G. A. (2002) Evidence for a genetic association between monoamine oxidase A and restless legs syndrome. Neurology 59, 215-219.
-
(2002)
Neurology
, vol.59
, pp. 215-219
-
-
Desautels, A.1
Turecki, G.2
Montplaisir, J.3
Brisebois, K.4
Sequeira, A.5
Adam, B.6
Rouleau, G.A.7
-
73
-
-
0036517472
-
A comprehensive review of genetic association studies
-
Hirschhorn, J. N., Lohmueller, K., Byrne, E. and Hirschhorn, K. (2002) A comprehensive review of genetic association studies. Genet. Med. 4, 45-61.
-
(2002)
Genet. Med
, vol.4
, pp. 45-61
-
-
Hirschhorn, J.N.1
Lohmueller, K.2
Byrne, E.3
Hirschhorn, K.4
-
74
-
-
0031912090
-
Genetic and familial aspects of narcolepsy
-
Mignot, E. (1998) Genetic and familial aspects of narcolepsy. Neurology 50, 16-22.
-
(1998)
Neurology
, vol.50
, pp. 16-22
-
-
Mignot, E.1
-
75
-
-
0035091595
-
Complex HLA-DR and DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups
-
Mignot E., Lin L., Rogers W., Honda Y., Qiu X., Lin X., Okun M., Hohjoh H., Miki T., Hsu S. et al. (2001) Complex HLA-DR and DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. Am. J. Hum. Genet. 68, 686-969.
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 686-969
-
-
Mignot, E.1
Lin, L.2
Rogers, W.3
Honda, Y.4
Qiu, X.5
Lin, X.6
Okun, M.7
Hohjoh, H.8
Miki, T.9
Hsu, S.10
-
76
-
-
4444287267
-
A narcolepsy susceptibility locus maps to a 5Mb region of chromosome 21q
-
Dauvilliers, Y., Blouim, J.-L., Neidhart, E., Carlander, B., Eliaou, J.-F., Antonorakis, S., Billiard, M. and Tafti, M. (2004) A narcolepsy susceptibility locus maps to a 5Mb region of chromosome 21q. Ann. Neurol. 56, 382-388.
-
(2004)
Ann. Neurol
, vol.56
, pp. 382-388
-
-
Dauvilliers, Y.1
Blouim, J.-L.2
Neidhart, E.3
Carlander, B.4
Eliaou, J.-F.5
Antonorakis, S.6
Billiard, M.7
Tafti, M.8
-
77
-
-
28744459556
-
Genes for normal sleep and sleep disorders
-
Tafti, M., Maret, S. and Dauvilliers, Y. (2005) Genes for normal sleep and sleep disorders Ann. Med. 37, 580-589.
-
(2005)
Ann. Med
, vol.37
, pp. 580-589
-
-
Tafti, M.1
Maret, S.2
Dauvilliers, Y.3
-
78
-
-
0034176716
-
Linkage of human narcolepsy with HLA association to chromosome 4p13q21
-
Nakayama, J., Miura, M., Honda M., Miki T., Honda, Y. and Arinami T. (2000) Linkage of human narcolepsy with HLA association to chromosome 4p13q21. Genomics 65, 84-86.
-
(2000)
Genomics
, vol.65
, pp. 84-86
-
-
Nakayama, J.1
Miura, M.2
Honda, M.3
Miki, T.4
Honda, Y.5
Arinami, T.6
-
79
-
-
0027462562
-
The occurrence of sleep disordered breathing in middle-aged adults
-
Young, T., Palta, M., Dempsey, J., Skatrud, J., Weber, S. and Bader, S. (1993) The occurrence of sleep disordered breathing in middle-aged adults. N. Engl. J. Med. 328, 1230-1235.
-
(1993)
N. Engl. J. Med
, vol.328
, pp. 1230-1235
-
-
Young, T.1
Palta, M.2
Dempsey, J.3
Skatrud, J.4
Weber, S.5
Bader, S.6
-
80
-
-
0033178851
-
Sleep-related breathing disorders in adults: Recommendations for syndrome definition and measurement techniques in clinical research
-
Sleep 22, 667-689
-
Sleep-related breathing disorders in adults: recommendations for syndrome definition and measurement techniques in clinical research. Report of an American Academy of Sleep Medicine Task Force (1999) Sleep 22, 667-689.
-
(1999)
Report of an American Academy of Sleep Medicine Task Force
-
-
-
81
-
-
0029023346
-
Familial aggregates in obstructive sleep apnea syndrome
-
Guilleminault, C., Partinen, M., Hollman, K., Powell, N. and Stroohs, R. (1995) Familial aggregates in obstructive sleep apnea syndrome. Chest 107, 1545-1551.
-
(1995)
Chest
, vol.107
, pp. 1545-1551
-
-
Guilleminault, C.1
Partinen, M.2
Hollman, K.3
Powell, N.4
Stroohs, R.5
-
82
-
-
4143129909
-
Genetic and environmental influences in sleep-disordered breathing in older male twins
-
Carmelli, D., Colrain, I. M., Swan, G. E. and Bliwise, D. L. (2004) Genetic and environmental influences in sleep-disordered breathing in older male twins. Sleep 27, 917-922.
-
(2004)
Sleep
, vol.27
, pp. 917-922
-
-
Carmelli, D.1
Colrain, I.M.2
Swan, G.E.3
Bliwise, D.L.4
-
83
-
-
23444441294
-
Genetic determinants of upper airway structures that predispose to obstructive sleep apnea
-
Schwab, R. J. (2005) Genetic determinants of upper airway structures that predispose to obstructive sleep apnea. Respir. Physiol. Neurobiol. 147, 289-298.
-
(2005)
Respir. Physiol. Neurobiol
, vol.147
, pp. 289-298
-
-
Schwab, R.J.1
-
84
-
-
0036128747
-
Genetics of the apnea hypopnea index in Caucasians and African Americans: I. Segregation analysis
-
Buxbaum, S. G., Elston, R. C., Tishler, P. V. and Redline, S. (2002) Genetics of the apnea hypopnea index in Caucasians and African Americans: I. Segregation analysis. Genet. Epidemiol. 3, 243-253.
-
(2002)
Genet. Epidemiol
, vol.3
, pp. 243-253
-
-
Buxbaum, S.G.1
Elston, R.C.2
Tishler, P.V.3
Redline, S.4
-
85
-
-
3442898790
-
Whole genome scan for obstructive sleep apnea and obesity in African-American families
-
Palmer, L. J., Buxbaum, S. G., Larkin, E. K., Patel, S. R., Elston, R. C., Tishler, P. V. and Redline S. (2004) Whole genome scan for obstructive sleep apnea and obesity in African-American families. Am. J. Respir. Crit. Care Med. 169, 1314-1321.
-
(2004)
Am. J. Respir. Crit. Care Med
, vol.169
, pp. 1314-1321
-
-
Palmer, L.J.1
Buxbaum, S.G.2
Larkin, E.K.3
Patel, S.R.4
Elston, R.C.5
Tishler, P.V.6
Redline, S.7
-
86
-
-
0037379890
-
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
-
Amiel J., Laudier B., Attie-Bitach T., Trang H., de Pontual L., Gener B., Trochet D., Etchevers H., Ray P., Simonneau M. et al. (2003) Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat. Genet. 4, 459-461.
-
(2003)
Nat. Genet
, vol.4
, pp. 459-461
-
-
Amiel, J.1
Laudier, B.2
Attie-Bitach, T.3
Trang, H.4
de Pontual, L.5
Gener, B.6
Trochet, D.7
Etchevers, H.8
Ray, P.9
Simonneau, M.10
-
87
-
-
0033804342
-
-
Zhang J., Zhao B., Gesongluobu, Sun Y., Wu Y., Pei W., Ye J., Hui R. and Liu L. (2000) Angiotensinconverting enzyme gene insertion/deletion (I/D) polymorphism in hypertensive patients with different degrees of obstructive sleep apnea. Hypertens. Res. Clin. Exp. 23, 407-411.
-
Zhang J., Zhao B., Gesongluobu, Sun Y., Wu Y., Pei W., Ye J., Hui R. and Liu L. (2000) Angiotensinconverting enzyme gene insertion/deletion (I/D) polymorphism in hypertensive patients with different degrees of obstructive sleep apnea. Hypertens. Res. Clin. Exp. 23, 407-411.
-
-
-
-
88
-
-
0035136677
-
An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome
-
Toh, K. L., Jones, C. R., He Y., Eide, E. J., Hinz, W. A., Virshup, D. M., Ptacek, L. J. and Fu, Y. H. (2001) An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome Science 291, 1040-1043.
-
(2001)
Science
, vol.291
, pp. 1040-1043
-
-
Toh, K.L.1
Jones, C.R.2
He, Y.3
Eide, E.J.4
Hinz, W.A.5
Virshup, D.M.6
Ptacek, L.J.7
Fu, Y.H.8
-
89
-
-
0032811966
-
Possible association of human leucocyte antigen DR1 with delayed sleep phase syndrome
-
Hohjoh, H., Takahashi, Y., Hatta, Y., Tanaka, H., Akaza, T., Tokunaga, K., Honda, Y. and Juji, T. (1999) Possible association of human leucocyte antigen DR1 with delayed sleep phase syndrome. Psychiat. Clin. Neurosci. 53, 527-529.
-
(1999)
Psychiat. Clin. Neurosci
, vol.53
, pp. 527-529
-
-
Hohjoh, H.1
Takahashi, Y.2
Hatta, Y.3
Tanaka, H.4
Akaza, T.5
Tokunaga, K.6
Honda, Y.7
Juji, T.8
-
90
-
-
0142244105
-
Two pedigrees of familial advanced sleep phase syndrome in Japan
-
Satoh, K., Mishima, K., Inoue, Y., Ebisawa, T. and Shimizu, T. (2003) Two pedigrees of familial advanced sleep phase syndrome in Japan. Sleep 26, 416-417.
-
(2003)
Sleep
, vol.26
, pp. 416-417
-
-
Satoh, K.1
Mishima, K.2
Inoue, Y.3
Ebisawa, T.4
Shimizu, T.5
-
91
-
-
0036897055
-
Familial Kleine-Levin Syndrome: Two siblings with unusually long hypersomnic spells
-
Katz, J. and Ropper, A. H. (2002) Familial Kleine-Levin Syndrome: two siblings with unusually long hypersomnic spells. Arch. Neurol. 59, 1959-1961.
-
(2002)
Arch. Neurol
, vol.59
, pp. 1959-1961
-
-
Katz, J.1
Ropper, A.H.2
-
92
-
-
0037058782
-
Kleine-Levin syndrome: An autoimmune hypothesis based on clinical and genetic analyses
-
Dauvilliers, Y., Mayer, G., Lecendreux, M., Neidhard, E., Peraita-Adrados, R., Sonka, K., Billiard, M. and Tafti, M. (2002) Kleine-Levin syndrome: an autoimmune hypothesis based on clinical and genetic analyses. Neurology 59, 1739-1745.
-
(2002)
Neurology
, vol.59
, pp. 1739-1745
-
-
Dauvilliers, Y.1
Mayer, G.2
Lecendreux, M.3
Neidhard, E.4
Peraita-Adrados, R.5
Sonka, K.6
Billiard, M.7
Tafti, M.8
|