-
1
-
-
0004235298
-
Diagnostic and Statistical Manual of Mental Disorders.
-
American Psychiatric Association. 4th edition, text revised. American Psychiatric Association, Washington, DC, USA.
-
American Psychiatric Association. (2000) Diagnostic and Statistical Manual of Mental Disorders. 4th edition, text revised. American Psychiatric Association, Washington, DC, USA.
-
(2000)
-
-
-
2
-
-
0036024261
-
A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19
-
Badenhop, R.F., Moses, M.J., Scimone, A., Mitchell, P.B., Ewen-White, K.R., Rosso, A., Donald, J.A., Adams, L.J. & Schofield, P.R. (2002) A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19. Mol Psychiatry 7, 851-859.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 851-859
-
-
Badenhop, R.F.1
Moses, M.J.2
Scimone, A.3
Mitchell, P.B.4
Ewen-White, K.R.5
Rosso, A.6
Donald, J.A.7
Adams, L.J.8
Schofield, P.R.9
-
3
-
-
38349128462
-
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
-
Baum, A.E., Akula, N., Cabanero, M., Cardona, I., Corona, W., Klemens, B., Schulze, T.G., Cichon, S., Rietschel, M., Nothen, M.M., Georgi, A., Schumacher, J., Schwarz, M., Abou Jamra, R., Hofels, S., Propping, P., Satagopan, J., Detera-Wadleigh, S.D., Hardy, J. & McMahon, F.J. (2008a) A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. Mol Psychiatry 13, 197-207.
-
(2008)
Mol Psychiatry
, vol.13
, pp. 197-207
-
-
Baum, A.E.1
Akula, N.2
Cabanero, M.3
Cardona, I.4
Corona, W.5
Klemens, B.6
Schulze, T.G.7
Cichon, S.8
Rietschel, M.9
Nothen, M.M.10
Georgi, A.11
Schumacher, J.12
Schwarz, M.13
Abou Jamra, R.14
Hofels, S.15
Propping, P.16
Satagopan, J.17
Detera-Wadleigh, S.D.18
Hardy, J.19
McMahon, F.J.20
more..
-
4
-
-
42349094538
-
Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement
-
Baum, A.E., Hamshere, M., Green, E., Cichon, S., Rietschel, M., Noethen, M.M., Craddock, N. & McMahon, F.J. (2008b) Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement. Mol Psychiatry 13, 466-467.
-
(2008)
Mol Psychiatry
, vol.13
, pp. 466-467
-
-
Baum, A.E.1
Hamshere, M.2
Green, E.3
Cichon, S.4
Rietschel, M.5
Noethen, M.M.6
Craddock, N.7
McMahon, F.J.8
-
5
-
-
0034013393
-
A randomized, placebo-controlled 12-month trial of divalproex and lithium in treatment of outpatients with bipolar I disorder. Divalproex Maintenance Study Group.
-
Bowden, C.L., Calabrese, J.R., McElroy, S.L., Gyulai, L., Wassef, A., Petty, F., Pope, H.G. Jr, Chou, J.C., Keck, P.E. Jr, Rhodes, L.J., Swann, A.C., Hirschfeld, R.M. & Wozniak, P.J. (2000) A randomized, placebo-controlled 12-month trial of divalproex and lithium in treatment of outpatients with bipolar I disorder. Divalproex Maintenance Study Group. Arch Gen Psychiatry 57, 481-489.
-
(2000)
Arch Gen Psychiatry
, vol.57
, pp. 481-489
-
-
Bowden, C.L.1
Calabrese, J.R.2
McElroy, S.L.3
Gyulai, L.4
Wassef, A.5
Petty, F.6
Pope Jr, H.G.7
Chou, J.C.8
Keck, P.E.9
Rhodes, L.J.10
Swann, A.C.11
Hirschfeld, R.M.12
Wozniak, P.J.13
-
6
-
-
0032803524
-
Genetics of bipolar disorder
-
Craddock, N. & Jones, I. (1999) Genetics of bipolar disorder. J Med Genet 36, 585-594.
-
(1999)
J Med Genet
, vol.36
, pp. 585-594
-
-
Craddock, N.1
Jones, I.2
-
7
-
-
0012060677
-
Migraine: Manifestations, Pathogenesis, and Management.
-
Oxford University Press, New York.
-
Davidoff, R.A. (2002) Migraine: Manifestations, Pathogenesis, and Management. Oxford University Press, New York.
-
(2002)
-
-
Davidoff, R.A.1
-
8
-
-
0037312922
-
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2
-
De Fusco, M., Marconi, R., Silvestri, L., Atorino, L., Rampoldi, L., Morgante, L., Ballabio, A., Aridon, P. & Casari, G. (2003) Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet 33, 192-196.
-
(2003)
Nat Genet
, vol.33
, pp. 192-196
-
-
De Fusco, M.1
Marconi, R.2
Silvestri, L.3
Atorino, L.4
Rampoldi, L.5
Morgante, L.6
Ballabio, A.7
Aridon, P.8
Casari, G.9
-
9
-
-
23044459961
-
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
-
Dichgans, M., Freilinger, T., Eckstein, G., Babini, E., Lorenz-Depiereux, B., Biskup, S., Ferrari, M.D., Herzog, J., Van Den Maagdenberg, A.M., Pusch, M. & Strom, T.M. (2005) Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet 366, 371-377.
-
(2005)
Lancet
, vol.366
, pp. 371-377
-
-
Dichgans, M.1
Freilinger, T.2
Eckstein, G.3
Babini, E.4
Lorenz-Depiereux, B.5
Biskup, S.6
Ferrari, M.D.7
Herzog, J.8
Van Den Maagdenberg, A.M.9
Pusch, M.10
Strom, T.M.11
-
10
-
-
60749105787
-
Is a family history of bipolar disorder a risk factor for migraine among affectively ill patients?
-
Dilsaver, S.C., Benazzi, F., Oedegaard, K.J., Fasmer, O.B. & Akiskal, H.S. (2009) Is a family history of bipolar disorder a risk factor for migraine among affectively ill patients? Psychopathology 42, 119-123.
-
(2009)
Psychopathology
, vol.42
, pp. 119-123
-
-
Dilsaver, S.C.1
Benazzi, F.2
Oedegaard, K.J.3
Fasmer, O.B.4
Akiskal, H.S.5
-
11
-
-
0030826382
-
Attention-deficit hyperactivity disorder with bipolar disorder: a familial subtype?
-
discussion 1387-1390
-
Faraone, S.V., Biederman, J., Mennin, D., Wozniak, J. & Spencer, T. (1997) Attention-deficit hyperactivity disorder with bipolar disorder: a familial subtype? J Am Acad Child Adolesc Psychiatry 36, 1378-1387; discussion 1387-1390.
-
(1997)
J Am Acad Child Adolesc Psychiatry
, vol.36
, pp. 1378-1387
-
-
Faraone, S.V.1
Biederman, J.2
Mennin, D.3
Wozniak, J.4
Spencer, T.5
-
12
-
-
20444412281
-
Molecular genetics of attention-deficit/hyperactivity disorder
-
Faraone, S.V., Perlis, R.H., Doyle, A.E., Smoller, J.W., Goralnick, J.J., Holmgren, M.A. & Sklar, P. (2005) Molecular genetics of attention-deficit/hyperactivity disorder. Biol Psychiatry 57, 1313-1323.
-
(2005)
Biol Psychiatry
, vol.57
, pp. 1313-1323
-
-
Faraone, S.V.1
Perlis, R.H.2
Doyle, A.E.3
Smoller, J.W.4
Goralnick, J.J.5
Holmgren, M.A.6
Sklar, P.7
-
13
-
-
0035741443
-
The prevalence of migraine in patients with bipolar and unipolar affective disorders
-
Fasmer, O.B. (2001) The prevalence of migraine in patients with bipolar and unipolar affective disorders. Cephalalgia 21, 894-899.
-
(2001)
Cephalalgia
, vol.21
, pp. 894-899
-
-
Fasmer, O.B.1
-
14
-
-
70350304394
-
Clinical and pathophysiological relations between migraine and mood disorders
-
Fasmer, O.B., Akiskal, H.S., Kelsoe, J.R. & Oedegaard, K.J. (2009a) Clinical and pathophysiological relations between migraine and mood disorders. Curr Psychiatry Rev 5, 93-109
-
(2009)
Curr Psychiatry Rev
, vol.5
, pp. 93-109
-
-
Fasmer, O.B.1
Akiskal, H.S.2
Kelsoe, J.R.3
Oedegaard, K.J.4
-
15
-
-
50449089356
-
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
-
Ferreira, M.A., O'Donovan, M.C., Meng, Y.A. et al. (2008) Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nat Genet 40, 1056-1058.
-
(2008)
Nat Genet
, vol.40
, pp. 1056-1058
-
-
Ferreira, M.A.1
O'Donovan, M.C.2
Meng, Y.A.3
-
16
-
-
0032856170
-
Migraine without aura: a population-based twin study
-
Gervil, M., Ulrich, V., Kyvik, K.O., Olesen, J. & Russell, M.B. (1999) Migraine without aura: a population-based twin study. Ann Neurol 46, 606-611.
-
(1999)
Ann Neurol
, vol.46
, pp. 606-611
-
-
Gervil, M.1
Ulrich, V.2
Kyvik, K.O.3
Olesen, J.4
Russell, M.B.5
-
17
-
-
77449123401
-
Bipolar symptoms in adult attention-deficit/hyperactivity disorder: a cross-sectional study of 510 clinically diagnosed patients and 417 population-based controls
-
Halmoy, A., Halleland, H., Dramsdahl, M., Bergsholm, P., Fasmer, O.B. & Haavik, J. (2010) Bipolar symptoms in adult attention-deficit/hyperactivity disorder: a cross-sectional study of 510 clinically diagnosed patients and 417 population-based controls. J Clin Psychiatry 71, 48-57.
-
(2010)
J Clin Psychiatry
, vol.71
, pp. 48-57
-
-
Halmoy, A.1
Halleland, H.2
Dramsdahl, M.3
Bergsholm, P.4
Fasmer, O.B.5
Haavik, J.6
-
19
-
-
0037269568
-
Screening for bipolar disorder in the community
-
Hirschfeld, R.M., Calabrese, J.R., Weissman, M.M., Reed, M., Davies, M.A., Frye, M.A., Keck, P.E. Jr, Lewis, L., McElroy, S.L., McNulty, J.P. & Wagner, K.D. (2003) Screening for bipolar disorder in the community. J Clin Psychiatry 64, 53-59.
-
(2003)
J Clin Psychiatry
, vol.64
, pp. 53-59
-
-
Hirschfeld, R.M.1
Calabrese, J.R.2
Weissman, M.M.3
Reed, M.4
Davies, M.A.5
Frye, M.A.6
Keck Jr, P.E.7
Lewis, L.8
McElroy, S.L.9
McNulty, J.P.10
Wagner, K.D.11
-
20
-
-
0028905597
-
Migraine and concomitant symptoms among 8167 adult twin pairs
-
Honkasalo, M.L., Kaprio, J., Winter, T., Heikkila, K., Sillanpaa, M. & Koskenvuo, M. (1995) Migraine and concomitant symptoms among 8167 adult twin pairs. Headache 35, 70-78.
-
(1995)
Headache
, vol.35
, pp. 70-78
-
-
Honkasalo, M.L.1
Kaprio, J.2
Winter, T.3
Heikkila, K.4
Sillanpaa, M.5
Koskenvuo, M.6
-
21
-
-
85035146867
-
The prevalence and correlates of adult ADHD in the United States: results from the National Comorbidity Survey Replication
-
Kessler, R.C., Adler, L., Barkley, R., Biederman, J., Conners, C.K., Demler, O., Faraone, S.V., Greenhill, L.L., Howes, M.J., Secnik, K., Spencer, T., Ustun, T.B., Walters, E.E. & Zaslavsky, A.M. (2006) The prevalence and correlates of adult ADHD in the United States: results from the National Comorbidity Survey Replication. Am J Psychiatry 163, 716-723.
-
(2006)
Am J Psychiatry
, vol.163
, pp. 716-723
-
-
Kessler, R.C.1
Adler, L.2
Barkley, R.3
Biederman, J.4
Conners, C.K.5
Demler, O.6
Faraone, S.V.7
Greenhill, L.L.8
Howes, M.J.9
Secnik, K.10
Spencer, T.11
Ustun, T.B.12
Walters, E.E.13
Zaslavsky, A.M.14
-
22
-
-
52949085789
-
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
-
Korn, J.M., Kuruvilla, F.G., McCarroll, S.A., Wysoker, A., Nemesh, J., Cawley, S., Hubbell, E., Veitch, J., Collins, P.J., Darvishi, K., Lee, C., Nizzari, M.M., Gabriel, S.B., Purcell, S., Daly, M.J. & Altshuler, D. (2008) Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nat Genet 40, 1253-1260.
-
(2008)
Nat Genet
, vol.40
, pp. 1253-1260
-
-
Korn, J.M.1
Kuruvilla, F.G.2
McCarroll, S.A.3
Wysoker, A.4
Nemesh, J.5
Cawley, S.6
Hubbell, E.7
Veitch, J.8
Collins, P.J.9
Darvishi, K.10
Lee, C.11
Nizzari, M.M.12
Gabriel, S.B.13
Purcell, S.14
Daly, M.J.15
Altshuler, D.16
-
23
-
-
0028818525
-
Genetic influence in headaches: a Swedish twin study
-
Larsson, B., Bille, B. & Pedersen, N.L. (1995) Genetic influence in headaches: a Swedish twin study. Headache 35, 513-519.
-
(1995)
Headache
, vol.35
, pp. 513-519
-
-
Larsson, B.1
Bille, B.2
Pedersen, N.L.3
-
24
-
-
55349115425
-
A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine
-
Ligthart, L., Nyholt, D.R., Hottenga, J.J., Distel, M.A., Willemsen, G. & Boomsma, D.I. (2008) A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine. Am J Med Genet B Neuropsychiatr Genet 147B, 1186-1195.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1186-1195
-
-
Ligthart, L.1
Nyholt, D.R.2
Hottenga, J.J.3
Distel, M.A.4
Willemsen, G.5
Boomsma, D.I.6
-
25
-
-
0141958271
-
Prevalence, clinical correlates, and treatment of migraine in bipolar disorder
-
Low, N.C., Du Fort, G.G. & Cervantes, P. (2003) Prevalence, clinical correlates, and treatment of migraine in bipolar disorder. Headache 43, 940-949.
-
(2003)
Headache
, vol.43
, pp. 940-949
-
-
Low, N.C.1
Du Fort, G.G.2
Cervantes, P.3
-
26
-
-
0032898367
-
Prevalence of migraine in bipolar disorder
-
Mahmood, T., Romans, S. & Silverstone, T. (1999) Prevalence of migraine in bipolar disorder. J Affect Disord 52, 239-241.
-
(1999)
J Affect Disord
, vol.52
, pp. 239-241
-
-
Mahmood, T.1
Romans, S.2
Silverstone, T.3
-
27
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll, S.A., Kuruvilla, F.G., Korn, J.M. et al. (2008) Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40, 1166-1174.
-
(2008)
Nat Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
-
28
-
-
33646936840
-
The prevalence and impact of migraine headache in bipolar disorder: results from the Canadian Community Health Survey
-
McIntyre, R.S., Konarski, J.Z., Wilkins, K., Bouffard, B., Soczynska, J.K. & Kennedy, S.H. (2006) The prevalence and impact of migraine headache in bipolar disorder: results from the Canadian Community Health Survey. Headache 46, 973-982.
-
(2006)
Headache
, vol.46
, pp. 973-982
-
-
McIntyre, R.S.1
Konarski, J.Z.2
Wilkins, K.3
Bouffard, B.4
Soczynska, J.K.5
Kennedy, S.H.6
-
29
-
-
25444466232
-
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q
-
McQueen, M.B., Devlin, B., Faraone, S.V. et al. (2005) Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. Am J Hum Genet 77, 582-595.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 582-595
-
-
McQueen, M.B.1
Devlin, B.2
Faraone, S.V.3
-
30
-
-
42949083431
-
Anticonvulsants in migraine prophylaxis: a Cochrane review
-
Mulleners, W.M. & Chronicle, E.P. (2008) Anticonvulsants in migraine prophylaxis: a Cochrane review. Cephalalgia 28, 585-597.
-
(2008)
Cephalalgia
, vol.28
, pp. 585-597
-
-
Mulleners, W.M.1
Chronicle, E.P.2
-
31
-
-
0028134880
-
Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative.
-
discussion 863-844
-
Nurnberger, J.I. Jr, Blehar, M.C., Kaufmann, C.A., York-Cooler, C., Simpson, S.G., Harkavy-Friedman, J., Severe, J.B., Malaspina, D. & Reich, T. (1994) Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative. Arch Gen Psychiatry 51, 849-859; discussion 863-844.
-
(1994)
Arch Gen Psychiatry
, vol.51
, pp. 849-859
-
-
Nurnberger Jr, J.I.1
Blehar, M.C.2
Kaufmann, C.A.3
York-Cooler, C.4
Simpson, S.G.5
Harkavy-Friedman, J.6
Severe, J.B.7
Malaspina, D.8
Reich, T.9
-
32
-
-
77649187448
-
A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11
-
Oedegaard, K.J., Greenwood, T.A., Lunde, A., Fasmer, O.B., Akiskal, H.S. & Kelsoe, J.R. (2010) A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11. J Affect Disord 122, 14-26.
-
(2010)
J Affect Disord
, vol.122
, pp. 14-26
-
-
Oedegaard, K.J.1
Greenwood, T.A.2
Lunde, A.3
Fasmer, O.B.4
Akiskal, H.S.5
Kelsoe, J.R.6
-
33
-
-
16044370232
-
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
-
Ophoff, R.A., Terwindt, G.M., Vergouwe, M.N., Van Eijk, R., Oefner, P.J., Hoffman, S.M., Lamerdin, J.E., Mohrenweiser, H.W., Bulman, D.E., Ferrari, M., Haan, J., Lindhout, D., Van Ommen, G.J., Hofker, M.H., Ferrari, M.D. & Frants, R.R. (1996) Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 87, 543-552.
-
(1996)
Cell
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
Terwindt, G.M.2
Vergouwe, M.N.3
Van Eijk, R.4
Oefner, P.J.5
Hoffman, S.M.6
Lamerdin, J.E.7
Mohrenweiser, H.W.8
Bulman, D.E.9
Ferrari, M.10
Haan, J.11
Lindhout, D.12
Van Ommen, G.J.13
Hofker, M.H.14
Ferrari, M.D.15
Frants, R.R.16
-
34
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M.A., Bender, D., Maller, J., Sklar, P., De Bakker, P.I., Daly, M.J. & Sham, P.C. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81, 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
35
-
-
43949118134
-
Whole-genome association study of bipolar disorder
-
Sklar, P., Smoller, J.W., Fan, J. et al. (2008) Whole-genome association study of bipolar disorder. Mol Psychiatry 13, 558-569.
-
(2008)
Mol Psychiatry
, vol.13
, pp. 558-569
-
-
Sklar, P.1
Smoller, J.W.2
Fan, J.3
-
36
-
-
67651158803
-
Genome-wide association study of bipolar disorder in European American and African American individuals
-
Smith, E.N., Bloss, C.S., Badner, J.A. et al. (2009) Genome-wide association study of bipolar disorder in European American and African American individuals. Mol Psychiatry 14, 755-763.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 755-763
-
-
Smith, E.N.1
Bloss, C.S.2
Badner, J.A.3
-
37
-
-
0242354132
-
Family, twin, and adoption studies of bipolar disorder
-
Smoller, J.W. & Finn, C.T. (2003) Family, twin, and adoption studies of bipolar disorder. Am J Med Genet C Semin Med Genet 123C, 48-58.
-
(2003)
Am J Med Genet C Semin Med Genet
, vol.123 C
, pp. 48-58
-
-
Smoller, J.W.1
Finn, C.T.2
-
38
-
-
34548547456
-
Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD)
-
Sobanski, E., Bruggemann, D., Alm, B., Kern, S., Deschner, M., Schubert, T., Philipsen, A. & Rietschel, M. (2007) Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD). Eur Arch Psychiatry Clin Neurosci 257, 371-377.
-
(2007)
Eur Arch Psychiatry Clin Neurosci
, vol.257
, pp. 371-377
-
-
Sobanski, E.1
Bruggemann, D.2
Alm, B.3
Kern, S.4
Deschner, M.5
Schubert, T.6
Philipsen, A.7
Rietschel, M.8
-
39
-
-
34249002104
-
Genetic models of migraine
-
Van De Ven, R.C., Kaja, S., Plomp, J.J., Frants, R.R., Van Den Maagdenberg, A.M. & Ferrari, M.D. (2007) Genetic models of migraine. Arch Neurol 64, 643-646.
-
(2007)
Arch Neurol
, vol.64
, pp. 643-646
-
-
Van De Ven, R.C.1
Kaja, S.2
Plomp, J.J.3
Frants, R.R.4
Van Den Maagdenberg, A.M.5
Ferrari, M.D.6
-
40
-
-
84969213492
-
Genome-wide association study of 14000 cases of seven common diseases and 3000 shared controls
-
WTCCC.
-
WTCCC. (2007) Genome-wide association study of 14000 cases of seven common diseases and 3000 shared controls. Nature 447, 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
|