-
1
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. 2002. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30(1): 97-101.
-
(2002)
Nat Genet
, vol.30
, Issue.1
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
2
-
-
42449161835
-
ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease
-
DOI: 10.1007/s00109-007-0299-6.
-
Arning L, Monte D, Hansen W, Wieczorek S, Jagiello P, Akkad DA, et al. 2008. ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease. J Mol Med 86(4): 485-490. DOI: 10.1007/s00109-007-0299-6.
-
(2008)
J Mol Med
, vol.86
, Issue.4
, pp. 485-490
-
-
Arning, L.1
Monte, D.2
Hansen, W.3
Wieczorek, S.4
Jagiello, P.5
Akkad, D.A.6
-
3
-
-
17344363640
-
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
-
DOI: 10.1038/1689.
-
Bashir R, Britton S, Strachan T, Keers S, Vafiadaki E, Lako M, et al. 1998. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet 20(1): 37-42. DOI: 10.1038/1689.
-
(1998)
Nat Genet
, vol.20
, Issue.1
, pp. 37-42
-
-
Bashir, R.1
Britton, S.2
Strachan, T.3
Keers, S.4
Vafiadaki, E.5
Lako, M.6
-
4
-
-
38349128462
-
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
-
Baum AE, Akula N, Cabanero M, Cardona I, Corona W, Klemens B, et al. 2008. A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. Mol Psychiatry 13(2): 197-207.
-
(2008)
Mol Psychiatry
, vol.13
, Issue.2
, pp. 197-207
-
-
Baum, A.E.1
Akula, N.2
Cabanero, M.3
Cardona, I.4
Corona, W.5
Klemens, B.6
-
5
-
-
23744490895
-
Population-based and family-based studies on the serotonin transporter gene polymorphisms and bipolar disorder: A systematic review and meta-analysis
-
DOI: 10.1038/sj.mp.4001663.
-
Cho HJ, Meira-Lima I, Cordeiro Q, Michelon L, Sham P, Vallada H, et al. 2005. Population-based and family-based studies on the serotonin transporter gene polymorphisms and bipolar disorder: A systematic review and meta-analysis. Mol Psychiatry 10(8): 771-781. DOI: 10.1038/sj.mp.4001663.
-
(2005)
Mol Psychiatry
, vol.10
, Issue.8
, pp. 771-781
-
-
Cho, H.J.1
Meira-Lima, I.2
Cordeiro, Q.3
Michelon, L.4
Sham, P.5
Vallada, H.6
-
6
-
-
33745689721
-
G72/G30 in schizophrenia and bipolar disorder: Review and meta-analysis
-
Detera-Wadleigh SD, McMahon FJ. 2006. G72/G30 in schizophrenia and bipolar disorder: Review and meta-analysis. Biol Psychiatry 60(2): 106-114.
-
(2006)
Biol Psychiatry
, vol.60
, Issue.2
, pp. 106-114
-
-
Detera-Wadleigh, S.D.1
McMahon, F.J.2
-
7
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
DOI: 10.1371/journal.pbio.1000294.
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB. 2010. Rare variants create synthetic genome-wide associations. PLoS Biol 8(1): e1000294. DOI: 10.1371/journal.pbio.1000294.
-
(2010)
PLoS Biol
, vol.8
, Issue.1
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
8
-
-
38149103580
-
Heritability of bipolar spectrum disorders. Unity or heterogeneity?
-
DOI: 10.1016/j.jad.2007.07.001.
-
Edvardsen J, Torgersen S, Roysamb E, Lygren S, Skre I, Onstad S, et al. 2008. Heritability of bipolar spectrum disorders. Unity or heterogeneity? J Affect Disord 106(3): 229-240. DOI: 10.1016/j.jad.2007.07.001.
-
(2008)
J Affect Disord
, vol.106
, Issue.3
, pp. 229-240
-
-
Edvardsen, J.1
Torgersen, S.2
Roysamb, E.3
Lygren, S.4
Skre, I.5
Onstad, S.6
-
9
-
-
57149111944
-
Navajo microvillous inclusion disease is due to a mutation in MYO5B
-
DOI: 10.1002/ajmg.a.32605.
-
Erickson RP, Larson-Thome K, Valenzuela RK, Whitaker SE, Shub MD. 2008. Navajo microvillous inclusion disease is due to a mutation in MYO5B. Am J Med Genet Part A 146A(24): 3117-3119. DOI: 10.1002/ajmg.a.32605.
-
(2008)
Am J Med Genet Part A
, vol.146 A
, Issue.24
, pp. 3117-3119
-
-
Erickson, R.P.1
Larson-Thome, K.2
Valenzuela, R.K.3
Whitaker, S.E.4
Shub, M.D.5
-
10
-
-
73949155114
-
Linkage disequilibrium mapping of the chromosome 6q 21-22. 31 bipolar I disorder susceptibility locus
-
DOI: 10.1002/ajmg.b.30942.
-
Fan J, Ionita-Laza I, McQueen MB, Devlin B, Purcell S, Faraone SV, et al. 2010. Linkage disequilibrium mapping of the chromosome 6q 21-22. 31 bipolar I disorder susceptibility locus. Am J Med Genet Part B 153B(1): 29-37. DOI: 10.1002/ajmg.b.30942.
-
(2010)
Am J Med Genet Part B
, vol.153 B
, Issue.1
, pp. 29-37
-
-
Fan, J.1
Ionita-Laza, I.2
McQueen, M.B.3
Devlin, B.4
Purcell, S.5
Faraone, S.V.6
-
11
-
-
50449089356
-
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
-
Ferreira MA, O'Donovan MC, Meng YA, Jones IR, Ruderfer DM, Jones L, 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
Jones, I.R.4
Ruderfer, D.M.5
Jones, L.6
-
12
-
-
33845887461
-
Methylenetetrahydrofolate reductase (MTHFR) genetic polymorphisms and psychiatric disorders: A HuGE review
-
Gilbody S, Lewis S, Lightfoot T. 2007. Methylenetetrahydrofolate reductase (MTHFR) genetic polymorphisms and psychiatric disorders: A HuGE review. Am J Epidemiol 165(1): 1-13.
-
(2007)
Am J Epidemiol
, vol.165
, Issue.1
, pp. 1-13
-
-
Gilbody, S.1
Lewis, S.2
Lightfoot, T.3
-
13
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
DOI: 10.1086/301592.
-
Kong A, Cox NJ. 1997. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 61(5): 1179-1188. DOI: 10.1086/301592.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.5
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
14
-
-
33745773735
-
Transmission distortion of BDNF variants to bipolar disorder type I patients from a South American population isolate
-
Kremeyer B, Herzberg I, Garcia J, Kerr E, Duque C, Parra V, et al. 2006. Transmission distortion of BDNF variants to bipolar disorder type I patients from a South American population isolate. Am J Med Genet Part B 141B(5): 435-439.
-
(2006)
Am J Med Genet Part B
, vol.141 B
, Issue.5
, pp. 435-439
-
-
Kremeyer, B.1
Herzberg, I.2
Garcia, J.3
Kerr, E.4
Duque, C.5
Parra, V.6
-
15
-
-
32344443827
-
Interactions of myosin vb with rab11 family members and cargoes traversing the plasma membrane recycling system
-
DOI: 10.1016/S0076-6879(05)03062-4.
-
Lapierre LA, Goldenring JR. 2005. Interactions of myosin vb with rab11 family members and cargoes traversing the plasma membrane recycling system. Methods Enzymol 403: 715-723. DOI: 10.1016/S0076-6879(05)03062-4.
-
(2005)
Methods Enzymol
, vol.403
, pp. 715-723
-
-
Lapierre, L.A.1
Goldenring, J.R.2
-
16
-
-
12944312689
-
Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders
-
Lasky-Su JA, Faraone SV, Glatt SJ, Tsuang MT. 2005. Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders. Am J Med Genet Part B 133B(1): 110-115.
-
(2005)
Am J Med Genet Part B
, vol.133 B
, Issue.1
, pp. 110-115
-
-
Lasky-Su, J.A.1
Faraone, S.V.2
Glatt, S.J.3
Tsuang, M.T.4
-
17
-
-
73249143065
-
Myosin Vb localises to nucleoli and associates with the RNA polymerase I transcription complex
-
DOI: 10.1002/cm.20408.
-
Lindsay AJ, McCaffrey MW. 2009. Myosin Vb localises to nucleoli and associates with the RNA polymerase I transcription complex. Cell Motil Cytoskeleton 66(12): 1057-1072. DOI: 10.1002/cm.20408.
-
(2009)
Cell Motil Cytoskeleton
, vol.66
, Issue.12
, pp. 1057-1072
-
-
Lindsay, A.J.1
McCaffrey, M.W.2
-
18
-
-
33645644972
-
Involvement of myosin Vb in glutamate receptor trafficking
-
DOI: 10.1074/jbc.M511725200.
-
Lise MF, Wong TP, Trinh A, Hines RM, Liu L, Kang R, et al. 2006. Involvement of myosin Vb in glutamate receptor trafficking. J Biol Chem 281(6): 3669-3678. DOI: 10.1074/jbc.M511725200.
-
(2006)
J Biol Chem
, vol.281
, Issue.6
, pp. 3669-3678
-
-
Lise, M.F.1
Wong, T.P.2
Trinh, A.3
Hines, R.M.4
Liu, L.5
Kang, R.6
-
19
-
-
17344365600
-
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
-
DOI: 10.1038/1682.
-
Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, et al. 1998. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet 20(1): 31-36. DOI: 10.1038/1682.
-
(1998)
Nat Genet
, vol.20
, Issue.1
, pp. 31-36
-
-
Liu, J.1
Aoki, M.2
Illa, I.3
Wu, C.4
Fardeau, M.5
Angelini, C.6
-
20
-
-
28844469295
-
Serotonin gene polymorphisms and bipolar I disorder: Focus on the serotonin transporter
-
DOI: 10.1080/07853890500357428.
-
Mansour HA, Talkowski ME, Wood J, Pless L, Bamne M, Chowdari KV, et al. 2005. Serotonin gene polymorphisms and bipolar I disorder: Focus on the serotonin transporter. Ann Med 37(8): 590-602. DOI: 10.1080/07853890500357428.
-
(2005)
Ann Med
, vol.37
, Issue.8
, pp. 590-602
-
-
Mansour, H.A.1
Talkowski, M.E.2
Wood, J.3
Pless, L.4
Bamne, M.5
Chowdari, K.V.6
-
21
-
-
55249087227
-
CBCL pediatric bipolar disorder profile and ADHD: Comorbidity and quantitative trait loci analysis
-
DOI: 10.1097/CHI.0b013e3181825a68.
-
McGough JJ, Loo SK, McCracken JT, Dang J, Clark S, Nelson SF, et al. 2008. CBCL pediatric bipolar disorder profile and ADHD: Comorbidity and quantitative trait loci analysis. J Am Acad Child Adolesc Psychiatry 47(10): 1151-1157. DOI: 10.1097/CHI.0b013e3181825a68.
-
(2008)
J Am Acad Child Adolesc Psychiatry
, vol.47
, Issue.10
, pp. 1151-1157
-
-
McGough, J.J.1
Loo, S.K.2
McCracken, J.T.3
Dang, J.4
Clark, S.5
Nelson, S.F.6
-
22
-
-
25444466232
-
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q
-
DOI: 10.1086/491603.
-
McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, 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(4): 582-595. DOI: 10.1086/491603.
-
(2005)
Am J Hum Genet
, vol.77
, Issue.4
, pp. 582-595
-
-
McQueen, M.B.1
Devlin, B.2
Faraone, S.V.3
Nimgaonkar, V.L.4
Sklar, P.5
Smoller, J.W.6
-
23
-
-
34247536530
-
Lifetime and 12-month prevalence of bipolar spectrum disorder in the National Comorbidity Survey replication
-
DOI: 10.1001/archpsyc.64.5.543.
-
Merikangas KR, Akiskal HS, Angst J, Greenberg PE, Hirschfeld RM, Petukhova M, et al. 2007. Lifetime and 12-month prevalence of bipolar spectrum disorder in the National Comorbidity Survey replication. Arch Gen Psychiatry 64(5): 543-552. DOI: 10.1001/archpsyc.64.5.543.
-
(2007)
Arch Gen Psychiatry
, vol.64
, Issue.5
, pp. 543-552
-
-
Merikangas, K.R.1
Akiskal, H.S.2
Angst, J.3
Greenberg, P.E.4
Hirschfeld, R.M.5
Petukhova, M.6
-
24
-
-
33846612007
-
Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD
-
DOI: 10.1186/1471-2377-6-44.
-
Momeni P, Schymick J, Jain S, Cookson MR, Cairns NJ, Greggio E, et al. 2006. Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD. BMC Neurol 6: 44. DOI: 10.1186/1471-2377-6-44.
-
(2006)
BMC Neurol
, vol.6
, pp. 44
-
-
Momeni, P.1
Schymick, J.2
Jain, S.3
Cookson, M.R.4
Cairns, N.J.5
Greggio, E.6
-
25
-
-
33846277959
-
Further evidence of MAO-A gene variants associated with bipolar disorder
-
DOI: 10.1002/ajmg.b.30380.
-
Muller DJ, Serretti A, Sicard T, Tharmalingam S, King N, Artioli P, et al. 2007. Further evidence of MAO-A gene variants associated with bipolar disorder. Am J Med Genet Part B 144B(1): 37-40. DOI: 10.1002/ajmg.b.30380.
-
(2007)
Am J Med Genet Part B
, vol.144 B
, Issue.1
, pp. 37-40
-
-
Muller, D.J.1
Serretti, A.2
Sicard, T.3
Tharmalingam, S.4
King, N.5
Artioli, P.6
-
26
-
-
52949112224
-
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity
-
DOI: 10.1038/ng.225.
-
Muller T, Hess MW, Schiefermeier N, Pfaller K, Ebner HL, Heinz-Erian P, et al. 2008. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity. Nat Genet 40(10): 1163-1165. DOI: 10.1038/ng.225.
-
(2008)
Nat Genet
, vol.40
, Issue.10
, pp. 1163-1165
-
-
Muller, T.1
Hess, M.W.2
Schiefermeier, N.3
Pfaller, K.4
Ebner, H.L.5
Heinz-Erian, P.6
-
27
-
-
0036724341
-
The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: Evidence from a family-based association study
-
Neves-Pereira M, Mundo E, Muglia P, King N, Macciardi F, Kennedy JL. 2002. The brain-derived neurotrophic factor gene confers susceptibility to bipolar disorder: Evidence from a family-based association study. Am J Hum Genet 71(3): 651-655.
-
(2002)
Am J Hum Genet
, vol.71
, Issue.3
, pp. 651-655
-
-
Neves-Pereira, M.1
Mundo, E.2
Muglia, P.3
King, N.4
Macciardi, F.5
Kennedy, J.L.6
-
28
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L. 2007. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81(3): 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, Issue.3
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
-
29
-
-
31544449191
-
Using linkage genome scans to improve power of association in genome scans
-
Roeder K, Bacanu SA, Wasserman L, Devlin B. 2006. Using linkage genome scans to improve power of association in genome scans. Am J Hum Genet 78(2): 243-252.
-
(2006)
Am J Hum Genet
, vol.78
, Issue.2
, pp. 243-252
-
-
Roeder, K.1
Bacanu, S.A.2
Wasserman, L.3
Devlin, B.4
-
30
-
-
36248977635
-
Improving power in genome-wide association studies: Weights tip the scale
-
DOI: 10.1002/gepi.20237.
-
Roeder K, Devlin B, Wasserman L. 2007. Improving power in genome-wide association studies: Weights tip the scale. Genet Epidemiol 31(7): 741-747. DOI: 10.1002/gepi.20237.
-
(2007)
Genet Epidemiol
, vol.31
, Issue.7
, pp. 741-747
-
-
Roeder, K.1
Devlin, B.2
Wasserman, L.3
-
31
-
-
0038054362
-
Rationale, design, and methods of the systematic treatment enhancement program for bipolar disorder (STEP-BD)
-
Sachs GS, Thase ME, Otto MW, Bauer M, Miklowitz D, Wisniewski SR, et al. 2003. Rationale, design, and methods of the systematic treatment enhancement program for bipolar disorder (STEP-BD). Biol Psychiatry 53(11): 1028-1042.
-
(2003)
Biol Psychiatry
, vol.53
, Issue.11
, pp. 1028-1042
-
-
Sachs, G.S.1
Thase, M.E.2
Otto, M.W.3
Bauer, M.4
Miklowitz, D.5
Wisniewski, S.R.6
-
32
-
-
0036347948
-
Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor
-
Sklar P, Gabriel SB, McInnis MG, Bennett P, Lim YM, Tsan G, et al. 2002. Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor. Mol Psychiatry 7(6): 579-593.
-
(2002)
Mol Psychiatry
, vol.7
, Issue.6
, pp. 579-593
-
-
Sklar, P.1
Gabriel, S.B.2
McInnis, M.G.3
Bennett, P.4
Lim, Y.M.5
Tsan, G.6
-
33
-
-
43949118134
-
Whole-genome association study of bipolar disorder
-
DOI: 10.1038/sj.mp.4002151.
-
Sklar P, Smoller JW, Fan J, Ferreira MA, Perlis RH, Chambert K, et al. 2008. Whole-genome association study of bipolar disorder. Mol Psychiatry 13(6): 558-569. DOI: 10.1038/sj.mp.4002151.
-
(2008)
Mol Psychiatry
, vol.13
, Issue.6
, pp. 558-569
-
-
Sklar, P.1
Smoller, J.W.2
Fan, J.3
Ferreira, M.A.4
Perlis, R.H.5
Chambert, K.6
-
34
-
-
0242354132
-
Family, twin, and adoption studies of bipolar disorder
-
Smoller JW, Finn CT. 2003. Family, twin, and adoption studies of bipolar disorder. Am J Med Genet Part C 123C(1): 48-58.
-
(2003)
Am J Med Genet Part C
, vol.123 C
, Issue.1
, pp. 48-58
-
-
Smoller, J.W.1
Finn, C.T.2
-
35
-
-
0036020892
-
A direct approach to false discovery rates
-
Retrieved from .
-
Storey JD. 2002. A direct approach to false discovery rates. J R Stat Soc Ser B Stat Methodol 64(3): 479-498. Retrieved from .
-
(2002)
J R Stat Soc Ser B Stat Methodol
, vol.64
, Issue.3
, pp. 479-498
-
-
Storey, J.D.1
-
36
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Retrieved from .
-
Whittemore AS, Halpern J. 1994. A class of tests for linkage using affected pedigree members. Biometrics 50(1): 118-127. Retrieved from .
-
(1994)
Biometrics
, vol.50
, Issue.1
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
37
-
-
79953034507
-
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder
-
Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, et al. 2010. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Mol Psychiatry 16: 429-441.
-
(2010)
Mol Psychiatry
, vol.16
, pp. 429-441
-
-
Williams, H.J.1
Norton, N.2
Dwyer, S.3
Moskvina, V.4
Nikolov, I.5
Carroll, L.6
-
38
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases,3,000 shared controls
-
WTCCC.. -.
-
WTCCC. 2007. Genome-wide association study of 14, 000 cases of seven common diseases, 3, 000 shared controls. Nature 447(7145): 661-678.
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
-
39
-
-
44949215794
-
Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis
-
DOI: 10.1016/j.neurobiolaging.2007.02.022.
-
Xiao S, Sato C, Kawarai T, Goodall EF, Pall HS, Zinman LH, et al. 2008. Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis. Neurobiol Aging 29(8): 1279-1282. DOI: 10.1016/j.neurobiolaging.2007.02.022.
-
(2008)
Neurobiol Aging
, vol.29
, Issue.8
, pp. 1279-1282
-
-
Xiao, S.1
Sato, C.2
Kawarai, T.3
Goodall, E.F.4
Pall, H.S.5
Zinman, L.H.6
|