-
1
-
-
81755176467
-
Advancing paternal age and risk of autism: New evidence from a population-based study and a meta-analysis of epidemiological studies
-
in press (e-pub ahead of print)
-
Hultman CM, Sandin S, Levine SZ, Lichtenstein P, Reichenberg A. Advancing paternal age and risk of autism: New evidence from a population-based study and a meta-analysis of epidemiological studies. Mol Psychiatry, in press (e-pub ahead of print).
-
Mol Psychiatry
-
-
Hultman, C.M.1
Sandin, S.2
Levine, S.Z.3
Lichtenstein, P.4
Reichenberg, A.5
-
2
-
-
0035045777
-
Advancing paternal age and the risk of schizophrenia
-
Malaspina D, Harlap S, Fennig S, Heiman D, Nahon D, Feldman D et al. Advancing paternal age and the risk of schizophrenia. Arch Gen Psychiatry 2001; 58: 361-367. (Pubitemid 32299532)
-
(2001)
Archives of General Psychiatry
, vol.58
, Issue.4
, pp. 361-367
-
-
Malaspina, D.1
Harlap, S.2
Fennig, S.3
Heiman, D.4
Nahon, D.5
Feldman, D.6
Susser, E.S.7
-
3
-
-
80052238644
-
Metaanalysis of paternal age and schizophrenia risk in male versus female offspring
-
in press (e-pub ahead of print)
-
Miller B, Messias E, Miettunen J, Alaraisanen A, Jarvelin MR, Koponen H et al. Metaanalysis of paternal age and schizophrenia risk in male versus female offspring. Schizophr Bull, in press (e-pub ahead of print).
-
Schizophr Bull
-
-
Miller, B.1
Messias, E.2
Miettunen, J.3
Alaraisanen, A.4
Jarvelin, M.R.5
Koponen, H.6
-
4
-
-
50949120272
-
Advancing paternal age and bipolar disorder
-
Frans EM, Sandin S, Reichenberg A, Lichtenstein P, Langstrom N, Hultman CM. Advancing paternal age and bipolar disorder. Arch Gen Psychiatry 2008; 65: 1034-1040.
-
(2008)
Arch Gen Psychiatry
, vol.65
, pp. 1034-1040
-
-
Frans, E.M.1
Sandin, S.2
Reichenberg, A.3
Lichtenstein, P.4
Langstrom, N.5
Hultman, C.M.6
-
5
-
-
28644451289
-
Paternal age and epilepsy in the offspring
-
DOI 10.1007/s10654-005-4250-2
-
Vestergaard M, Mork A, Madsen KM, Olsen J. Paternal age and epilepsy in the offspring. Eur J Epidemiol 2005; 20: 1003-1005. (Pubitemid 41752618)
-
(2005)
European Journal of Epidemiology
, vol.20
, Issue.12
, pp. 1003-1005
-
-
Vestergaard, M.1
Mork, A.2
Madsen, K.M.3
Olsen, J.4
-
6
-
-
63549147533
-
Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood
-
Saha S, Barnett AG, Foldi C, Burne TH, Eyles DW, Buka SL et al. Advanced paternal age is associated with impaired neurocognitive outcomes during infancy and childhood. PLoS Med 2009; 6: E40.
-
(2009)
PLoS Med
, vol.6
-
-
Saha, S.1
Barnett, A.G.2
Foldi, C.3
Burne, T.H.4
Eyles, D.W.5
Buka, S.L.6
-
7
-
-
33746741125
-
Copy number variation: New insights in genome diversity
-
DOI 10.1101/gr.3677206
-
Freeman JL, Perry GH, Feuk L, Redon R, McCarroll SA, Altshuler DM et al. Copy number variation: New insights in genome diversity. Genome Res 2006; 16: 949-961. (Pubitemid 44162254)
-
(2006)
Genome Research
, vol.16
, Issue.8
, pp. 949-961
-
-
Freeman, J.L.1
Perry, G.H.2
Feuk, L.3
Redon, R.4
McCarroll, S.A.5
Altshuler, D.M.6
Aburatani, H.7
Jones, K.W.8
Tyler-Smith, C.9
Hurles, M.E.10
Carter, N.P.11
Scherer, S.W.12
Lee, C.13
-
8
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
DOI 10.1126/science.1098918
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P et al. Large-scale copy number polymorphism in the human genome. Science 2004; 305: 525-528. (Pubitemid 38971344)
-
(2004)
Science
, vol.305
, Issue.5683
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
Maner, S.7
Massa, H.8
Walker, M.9
Chi, M.10
Navin, N.11
Lucito, R.12
Healy, J.13
Hicks, J.14
Ye, K.15
Reiner, A.16
Gilliam, T.C.17
Trask, B.18
Patterson, N.19
Zetterberg, A.20
Wigler, M.21
more..
-
9
-
-
20544462642
-
Segmental duplications and copy-number variation in the human genome
-
DOI 10.1086/431652
-
Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, Vallente RU et al. Segmental duplications and copy-number variation in the human genome. Am J Hum Genet 2005; 77: 78-88. (Pubitemid 40848038)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.1
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
Vallente, R.U.6
Pertz, L.M.7
Clark, R.A.8
Schwartz, S.9
Segraves, R.10
Oseroff, V.V.11
Albertson, D.G.12
Pinkel, D.13
Eichler, E.E.14
-
10
-
-
4444242992
-
Genomic segmental polymorphisms in inbred mouse strains
-
DOI 10.1038/ng1417
-
Li J, Jiang T, Mao JH, Balmain A, Peterson L, Harris C et al. Genomic segmental polymorphisms in inbred mouse strains. Nat Genet 2004; 36: 952-954. (Pubitemid 39167489)
-
(2004)
Nature Genetics
, vol.36
, Issue.9
, pp. 952-954
-
-
Li, J.1
Jiang, T.2
Mao, J.-H.3
Balmain, A.4
Peterson, L.5
Harris, C.6
Rao, P.H.7
Havlak, P.8
Gibbs, R.9
Cai, W.-W.10
-
11
-
-
33846614650
-
A high-resolution map of segmental DNA copy number variation in the mouse genome
-
Graubert TA, Cahan P, Edwin D, Selzer RR, Richmond TA, Eis PS et al. A high-resolution map of segmental DNA copy number variation in the mouse genome. PLoS Genet 2007; 3: E3.
-
(2007)
PLoS Genet
, vol.3
-
-
Graubert, T.A.1
Cahan, P.2
Edwin, D.3
Selzer, R.R.4
Richmond, T.A.5
Eis, P.S.6
-
12
-
-
65949085347
-
Microdeletion/ duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
-
Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C et al. Microdeletion/ duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J Med Genet 2009; 46: 242-248.
-
(2009)
J Med Genet
, vol.46
, pp. 242-248
-
-
Miller, D.T.1
Shen, Y.2
Weiss, L.A.3
Korn, J.4
Anselm, I.5
Bridgemohan, C.6
-
13
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466: 368-372.
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
Anney, R.4
Merico, D.5
Regan, R.6
-
14
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
DOI 10.1126/science.1138659
-
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T et al. Strong association of de novo copy number mutations with autism. Science 2007; 316: 445-449. (Pubitemid 46651493)
-
(2007)
Science
, vol.316
, Issue.5823
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Yamrom, B.7
Yoon, S.8
Krasnitz, A.9
Kendall, J.10
Leotta, A.11
Pai, D.12
Zhang, R.13
Lee, Y.-H.14
Hicks, J.15
Spence, S.J.16
Lee, A.T.17
Puura, K.18
Lehtimaki, T.19
Ledbetter, D.20
Gregersen, P.K.21
Bregman, J.22
Sutcliffe, J.S.23
Jobanputra, V.24
Chung, W.25
Warburton, D.26
King, M.-C.27
Skuse, D.28
Geschwind, D.H.29
Gilliam, T.C.30
Ye, K.31
Wigler, M.32
more..
-
15
-
-
70350626873
-
Microduplications of 16p11.2 are associated with schizophrenia
-
McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S et al. Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet 2009; 41: 1223-1227.
-
(2009)
Nat Genet
, vol.41
, pp. 1223-1227
-
-
McCarthy, S.E.1
Makarov, V.2
Kirov, G.3
Addington, A.M.4
McClellan, J.5
Yoon, S.6
-
16
-
-
77955379566
-
Copy number variations in schizophrenia: Critical review and new perspectives on concepts of genetics and disease
-
Bassett AS, Scherer SW, Brzustowicz LM. Copy number variations in schizophrenia: Critical review and new perspectives on concepts of genetics and disease. Am J Psychiatry 2010; 167: 899-914.
-
(2010)
Am J Psychiatry
, vol.167
, pp. 899-914
-
-
Bassett, A.S.1
Scherer, S.W.2
Brzustowicz, L.M.3
-
17
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
DOI 10.1038/ng.162, PII NG162
-
Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet 2008; 40: 880-885. (Pubitemid 351913650)
-
(2008)
Nature Genetics
, vol.40
, Issue.7
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
Van Rensburg, E.J.4
Gogos, J.A.5
Karayiorgou, M.6
-
18
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia C
-
International Schizophrenia C. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
19
-
-
77956628767
-
Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
-
Mefford HC, Muhle H, Ostertag P, von Spiczak S, Buysse K, Baker C et al. Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet 2010; 6: E1000962.
-
(2010)
PLoS Genet
, vol.6
-
-
Mefford, H.C.1
Muhle, H.2
Ostertag, P.3
Von Spiczak, S.4
Buysse, K.5
Baker, C.6
-
20
-
-
59149096726
-
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
-
Helbig I, Mefford HC, Sharp AJ, Guipponi M, Fichera M, Franke A et al. 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nat Genet 2009; 41: 160-162.
-
(2009)
Nat Genet
, vol.41
, pp. 160-162
-
-
Helbig, I.1
Mefford, H.C.2
Sharp, A.J.3
Guipponi, M.4
Fichera, M.5
Franke, A.6
-
21
-
-
25444432040
-
Diagnostic genome profiling in mental retardation
-
DOI 10.1086/491719
-
de Vries BB, Pfundt R, Leisink M, Koolen DA, Vissers LE, Janssen IM et al. Diagnostic genome profiling in mental retardation. Am J Hum Genet 2005; 77: 606-616. (Pubitemid 41361607)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.4
, pp. 606-616
-
-
De Vries, B.B.A.1
Pfundt, R.2
Leisink, M.3
Koolen, D.A.4
Vissers, L.E.L.M.5
Janssen, I.M.6
Van Reijmersdal, S.7
Nillesen, W.M.8
Huys, E.H.L.P.G.9
De Leeuw, N.10
Smeets, D.11
Sistermans, E.A.12
Feuth, T.13
Van Ravenswaaij-Arts, C.M.A.14
Van Kessel, A.G.15
Schoenmakers, E.F.P.M.16
Brunner, H.G.17
Veltman, J.A.18
-
22
-
-
34848904050
-
Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation
-
DOI 10.1086/521274
-
Wagenstaller J, Spranger S, Lorenz-Depiereux B, Kazmierczak B, Nathrath M, Wahl D et al. Copy-number variations measured by single-nucleotide- polymorphism oligonucleotide arrays in patients with mental retardation. Am J Hum Genet 2007; 81: 768-779. (Pubitemid 47596544)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.4
, pp. 768-779
-
-
Wagenstaller, J.1
Spranger, S.2
Lorenz-Depiereux, B.3
Kazmierczak, B.4
Nathrath, M.5
Wahl, D.6
Heye, B.7
Glaser, D.8
Liebscher, V.9
Meitinger, T.10
Strom, T.M.11
-
23
-
-
56749179965
-
Phenotypic variations on the theme of CNVs
-
O'Donovan MC, Kirov G, Owen MJ. Phenotypic variations on the theme of CNVs. Nat Genet 2008; 40: 1392-1393.
-
(2008)
Nat Genet
, vol.40
, pp. 1392-1393
-
-
O'Donovan, M.C.1
Kirov, G.2
Owen, M.J.3
-
24
-
-
0020580436
-
Decrease of learning capacity in offspring with increasing paternal age in the rat
-
Auroux M. Decrease of learning capacity in offspring with increasing paternal age in the rat. Teratology 1983; 27: 141-148. (Pubitemid 13088881)
-
(1983)
Teratology
, vol.27
, Issue.2
, pp. 141-148
-
-
Auroux, M.1
-
25
-
-
77949537571
-
Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: A mouse model
-
Smith RG, Kember RL, Mill J, Fernandes C, Schalkwyk LC, Buxbaum JD et al. Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: A mouse model. PLoS One 2009; 4: E8456.
-
(2009)
PLoS One
, vol.4
-
-
Smith, R.G.1
Kember, R.L.2
Mill, J.3
Fernandes, C.4
Schalkwyk, L.C.5
Buxbaum, J.D.6
-
26
-
-
59949093273
-
Long-term effects of delayed fatherhood in mice on postnatal development and behavioral traits of offspring
-
Garcia-Palomares S, Pertusa JF, Minarro J, Garcia-Perez MA, Hermenegildo C, Rausell F et al. Long-term effects of delayed fatherhood in mice on postnatal development and behavioral traits of offspring. Biol Reprod 2009; 80: 337-342.
-
(2009)
Biol Reprod
, vol.80
, pp. 337-342
-
-
Garcia-Palomares, S.1
Pertusa, J.F.2
Minarro, J.3
Garcia-Perez, M.A.4
Hermenegildo, C.5
Rausell, F.6
-
27
-
-
75749145826
-
Advanced paternal age is associated with alterations in discrete behavioural domains and cortical neuroanatomy of C57BL/6J mice
-
Foldi CJ, Eyles DW, McGrath JJ, Burne TH. Advanced paternal age is associated with alterations in discrete behavioural domains and cortical neuroanatomy of C57BL/6J mice. Eur J Neurosci 2010; 31: 556-564.
-
(2010)
Eur J Neurosci
, vol.31
, pp. 556-564
-
-
Foldi, C.J.1
Eyles, D.W.2
McGrath, J.J.3
Burne, T.H.4
-
28
-
-
46249114293
-
Mouse segmental duplication and copy number variation
-
DOI 10.1038/ng.172, PII NG172
-
She X, Cheng Z, Zollner S, Church DM, Eichler EE. Mouse segmental duplication and copy number variation. Nat Genet 2008; 40: 909-914. (Pubitemid 351913656)
-
(2008)
Nature Genetics
, vol.40
, Issue.7
, pp. 909-914
-
-
She, X.1
Cheng, Z.2
Zollner, S.3
Church, D.M.4
Eichler, E.E.5
-
29
-
-
55249123866
-
Analysis of copy number variation using quantitative interspecies competitive PCR
-
Williams NM, Williams H, Majounie E, Norton N, Glaser B, Morris HR et al. Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Res 2008; 36: E112.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Williams, N.M.1
Williams, H.2
Majounie, E.3
Norton, N.4
Glaser, B.5
Morris, H.R.6
-
30
-
-
25444435693
-
Simultaneous quantitative and allelespecific expression analysis with real competitive PCR
-
Ding C, Maier E, Roscher AA, Braun A, Cantor CR. Simultaneous quantitative and allelespecific expression analysis with real competitive PCR. BMC Genet 2004; 5: 8.
-
(2004)
BMC Genet
, vol.5
, pp. 8
-
-
Ding, C.1
Maier, E.2
Roscher, A.A.3
Braun, A.4
Cantor, C.R.5
-
32
-
-
51449110541
-
A searchable database of genetic evidence for psychiatric disorders
-
Konneker T, Barnes T, Furberg H, Losh M, Bulik CM, Sullivan PF. A searchable database of genetic evidence for psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 671-675.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 671-675
-
-
Konneker, T.1
Barnes, T.2
Furberg, H.3
Losh, M.4
Bulik, C.M.5
Sullivan, P.F.6
-
33
-
-
13444266370
-
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
-
DOI 10.1093/nar/gki033
-
Hamosh A, Scott AF, Amberger JS, Bocchini CA, McKusick VA. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res 2005; 33(Database issue): D514-D517. (Pubitemid 40207927)
-
(2005)
Nucleic Acids Research
, vol.33
, Issue.DATABASE ISS.
-
-
Hamosh, A.1
Scott, A.F.2
Amberger, J.S.3
Bocchini, C.A.4
McKusick, V.A.5
-
35
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
DOI 10.1038/ng1416
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y et al. Detection of largescale variation in the human genome. Nat Genet 2004; 36: 949-951. (Pubitemid 39167488)
-
(2004)
Nature Genetics
, vol.36
, Issue.9
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
36
-
-
33751527925
-
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome
-
DOI 10.1159/000095916
-
Zhang J, Feuk L, Duggan GE, Khaja R, Scherer SW. Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome. Cytogenet Genome Res 2006; 115: 205-214. (Pubitemid 44832022)
-
(2006)
Cytogenetic and Genome Research
, vol.115
, Issue.3-4
, pp. 205-214
-
-
Zhang, J.1
Feuk, L.2
Duggan, G.E.3
Khaja, R.4
Scherer, S.W.5
-
37
-
-
0347683377
-
1 receptor gene associated with alcoholism
-
DOI 10.1016/j.biopsych.2003.07.008
-
Miyatake R, Furukawa A, Matsushita S, Higuchi S, Suwaki H. Functional polymorphisms in the sigma1 receptor gene associated with alcoholism. Biol Psychiatry 2004; 55: 85-90. (Pubitemid 38045437)
-
(2004)
Biological Psychiatry
, vol.55
, Issue.1
, pp. 85-90
-
-
Miyatake, R.1
Furukawa, A.2
Matsushita, S.3
Higuchi, S.4
Suwaki, H.5
-
38
-
-
62849105979
-
Association between sigma-1 receptor gene polymorphism and prefrontal hemodynamic response induced by cognitive activation in schizophrenia
-
Takizawa R, Hashimoto K, Tochigi M, Kawakubo Y, Marumo K, Sasaki T et al. Association between sigma-1 receptor gene polymorphism and prefrontal hemodynamic response induced by cognitive activation in schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 2009; 33: 491-498.
-
(2009)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.33
, pp. 491-498
-
-
Takizawa, R.1
Hashimoto, K.2
Tochigi, M.3
Kawakubo, Y.4
Marumo, K.5
Sasaki, T.6
-
39
-
-
78249273602
-
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degenerationmotor neuron disease
-
Luty AA, Kwok JB, Dobson-Stone C, Loy CT, Coupland KG, Karlstrom H et al. Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degenerationmotor neuron disease. Ann Neurol 2010; 68: 639-649.
-
(2010)
Ann Neurol
, vol.68
, pp. 639-649
-
-
Luty, A.A.1
Kwok, J.B.2
Dobson-Stone, C.3
Loy, C.T.4
Coupland, K.G.5
Karlstrom, H.6
-
40
-
-
66249097733
-
A high-density SNP genome-wide linkage scan in a large autism extended pedigree
-
Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M et al. A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Mol Psychiatry 2009; 14: 590-600.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 590-600
-
-
Allen-Brady, K.1
Miller, J.2
Matsunami, N.3
Stevens, J.4
Block, H.5
Farley, M.6
-
41
-
-
43949122950
-
Genomewide association for schizophrenia in the CATIE study: Results of stage 1
-
DOI 10.1038/mp.2008.25, PII MP200825
-
Sullivan PF, Lin D, Tzeng JY, van den Oord E, Perkins D, Stroup TS et al. Genomewide association for schizophrenia in the CATIE study: Results of stage 1. Mol Psychiatry 2008; 13: 570-584. (Pubitemid 351704941)
-
(2008)
Molecular Psychiatry
, vol.13
, Issue.6
, pp. 570-584
-
-
Sullivan, P.F.1
Lin, D.2
Tzeng, J.-Y.3
Van Den Oord, E.4
Perkins, D.5
Stroup, T.S.6
Wagner, M.7
Lee, S.8
Wright, F.A.9
Zou, F.10
Liu, W.11
Downing, A.M.12
Lieberman, J.13
Close, S.L.14
-
42
-
-
43949118134
-
Whole-genome association study of bipolar disorder
-
DOI 10.1038/sj.mp.4002151, PII 4002151
-
Sklar P, Smoller JW, Fan J, Ferreira MA, Perlis RH, Chambert K et al. Whole-genome association study of bipolar disorder. Mol Psychiatry 2008; 13: 558-569. (Pubitemid 351704939)
-
(2008)
Molecular Psychiatry
, vol.13
, Issue.6
, pp. 558-569
-
-
Sklar, P.1
Smoller, J.W.2
Fan, J.3
Ferreira, M.A.R.4
Perlis, R.H.5
Chambert, K.6
Nimgaonkar, V.L.7
McQueen, M.B.8
Faraone, S.V.9
Kirby, A.10
De Bakker, P.I.W.11
Ogdie, M.N.12
Thase, M.E.13
Sachs, G.S.14
Todd-Brown, K.15
Gabriel, S.B.16
Sougnez, C.17
Gates, C.18
Blumenstiel, B.19
Defelice, M.20
Ardlie, K.G.21
Franklin, J.22
Muir, W.J.23
McGhee, K.A.24
MacIntyre, D.J.25
McLean, A.26
VanBeck, M.27
McQuillin, A.28
Bass, N.J.29
Robinson, M.30
Lawrence, J.31
Anjorin, A.32
Curtis, D.33
Scolnick, E.M.34
Daly, M.J.35
Blackwood, D.H.36
Gurling, H.M.37
Purcell, S.M.38
more..
-
43
-
-
57349131186
-
Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder
-
Zhou K, Dempfle A, Arcos-Burgos M, Bakker SC, Banaschewski T, Biederman J et al. Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2008; 147B: 1392-1398.
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1392-1398
-
-
Zhou, K.1
Dempfle, A.2
Arcos-Burgos, M.3
Bakker, S.C.4
Banaschewski, T.5
Biederman, J.6
-
44
-
-
79955569025
-
Genomewide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
-
Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D et al. Genomewide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proc Natl Acad Sci USA 2011; 108: 7119-7124.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 7119-7124
-
-
Schumann, G.1
Coin, L.J.2
Lourdusamy, A.3
Charoen, P.4
Berger, K.H.5
Stacey, D.6
-
45
-
-
41149140859
-
Epigenomic profiling reveals DNA-methylation changes associated with major psychosis
-
DOI 10.1016/j.ajhg.2008.01.008, PII S0002929708001481
-
Mill J, Tang T, Kaminsky Z, Khare T, Yazdanpanah S, Bouchard L et al. Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am J Hum Genet 2008; 82: 696-711. (Pubitemid 351726115)
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.3
, pp. 696-711
-
-
Mill, J.1
Tang, T.2
Kaminsky, Z.3
Khare, T.4
Yazdanpanah, S.5
Bouchard, L.6
Jia, P.7
Assadzadeh, A.8
Flanagan, J.9
Schumacher, A.10
Wang, S.-C.11
Petronis, A.12
-
46
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, Andrews TD et al. Global variation in copy number in the human genome. Nature 2006; 444: 444-454. (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
47
-
-
84975804424
-
Mapping copy number variation by population-scale genome sequencing
-
Mills RE, Walter K, Stewart C, Handsaker RE, Chen K, Alkan C et al. Mapping copy number variation by population-scale genome sequencing. Nature 2011; 470: 59-65.
-
(2011)
Nature
, vol.470
, pp. 59-65
-
-
Mills, R.E.1
Walter, K.2
Stewart, C.3
Handsaker, R.E.4
Chen, K.5
Alkan, C.6
-
48
-
-
77952296952
-
Towards a comprehensive structural variation map of an individual human genome
-
Pang AW, MacDonald JR, Pinto D, Wei J, Rafiq MA, Conrad DF et al. Towards a comprehensive structural variation map of an individual human genome. Genome Biol 2010; 11: R52.
-
(2010)
Genome Biol
, vol.11
-
-
Pang, A.W.1
MacDonald, J.R.2
Pinto, D.3
Wei, J.4
Rafiq, M.A.5
Conrad, D.F.6
-
49
-
-
69749090013
-
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
-
McKernan KJ, Peckham HE, Costa GL, McLaughlin SF, Fu Y, Tsung EF et al. Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding. Genome Res 2009; 19: 1527-1541.
-
(2009)
Genome Res
, vol.19
, pp. 1527-1541
-
-
McKernan, K.J.1
Peckham, H.E.2
Costa, G.L.3
McLaughlin, S.F.4
Fu, Y.5
Tsung, E.F.6
-
50
-
-
35648976118
-
The diploid genome sequence of an individual human
-
Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP et al. The diploid genome sequence of an individual human. PLoS Biol 2007; 5: E254.
-
(2007)
PLoS Biol
, vol.5
-
-
Levy, S.1
Sutton, G.2
Ng, P.C.3
Feuk, L.4
Halpern, A.L.5
Walenz, B.P.6
-
51
-
-
77958188414
-
Reference-unbiased copy number variant analysis using CGH microarrays
-
Ju YS, Hong D, Kim S, Park SS, Lee S, Park H et al. Reference-unbiased copy number variant analysis using CGH microarrays. Nucleic Acids Res 2010; 38: E190.
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Ju, Y.S.1
Hong, D.2
Kim, S.3
Park, S.S.4
Lee, S.5
Park, H.6
-
52
-
-
65449139457
-
Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder
-
Cusco I, Medrano A, Gener B, Vilardell M, Gallastegui F, Villa O et al. Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. Hum Mol Genet 2009; 18: 1795-1804.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1795-1804
-
-
Cusco, I.1
Medrano, A.2
Gener, B.3
Vilardell, M.4
Gallastegui, F.5
Villa, O.6
-
53
-
-
77952887857
-
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
-
Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT et al. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol Psychiatry 2010; 15: 637-646.
-
(2010)
Mol Psychiatry
, vol.15
, pp. 637-646
-
-
Elia, J.1
Gai, X.2
Xie, H.M.3
Perin, J.C.4
Geiger, E.5
Glessner, J.T.6
-
54
-
-
80052309623
-
-
DECIPHER. DECIPHERv5.1. The DECIPHER consortium, Wellcome Trust Sanger Institute, Hinxton, 2011
-
DECIPHER. DECIPHERv5.1. The DECIPHER consortium, Wellcome Trust Sanger Institute, Hinxton, 2011.
-
-
-
-
55
-
-
77955301410
-
A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism
-
Huang XL, Zou YS, Maher TA, Newton S, Milunsky JM. A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism. Am J Med Genet A 2010; 152A: 2112-2114.
-
(2010)
Am J Med Genet A
, vol.152 A
, pp. 2112-2114
-
-
Huang, X.L.1
Zou, Y.S.2
Maher, T.A.3
Newton, S.4
Milunsky, J.M.5
-
56
-
-
0021328139
-
Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/splitfoot malformation
-
Pfeiffer RA. Interstitial deletion of a chromosome 7 (q11.2q22.1) in a child with splithand/ splitfoot malformation. Ann Genet 1984; 27: 45-48. (Pubitemid 14147251)
-
(1984)
Annales de Genetique
, vol.27
, Issue.1
, pp. 45-48
-
-
Pfeiffer, R.A.1
-
57
-
-
0026641459
-
Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant
-
Gillar PJ, Kaye CI, Ryan SG, Moore CM. Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant. Am J Med Genet 1992; 44: 138-141.
-
(1992)
Am J Med Genet
, vol.44
, pp. 138-141
-
-
Gillar, P.J.1
Kaye, C.I.2
Ryan, S.G.3
Moore, C.M.4
-
58
-
-
0021361253
-
Terminal and interstitial deletions of the long arm of chromosome 7: A review with five new cases
-
Young RS, Weaver DD, Kukolich MK, Heerema NA, Palmer CG, Kawira EL et al. Terminal and interstitial deletions of the long arm of chromosome 7: A review with five new cases. Am J Med Genet 1984; 17: 437-450. (Pubitemid 14189145)
-
(1984)
American Journal of Medical Genetics
, vol.17
, Issue.2
, pp. 437-450
-
-
Young, R.S.1
Weaver, D.D.2
Kukolich, M.K.3
-
59
-
-
0023735743
-
Zellweger syndrome and a microdeletion of the proximal long arm of chromosome 7
-
Naritomi K, Hyakuna N, Suzuki Y, Orii T, Hirayama K. Zellweger syndrome and a microdeletion of the proximal long arm of chromosome 7. Hum Genet 1988; 80: 201-202.
-
(1988)
Hum Genet
, vol.80
, pp. 201-202
-
-
Naritomi, K.1
Hyakuna, N.2
Suzuki, Y.3
Orii, T.4
Hirayama, K.5
-
60
-
-
38749099110
-
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
-
DOI 10.1016/j.ajhg.2007.09.017, PII S0002929707000237
-
Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. Am J Hum Genet 2008; 82: 165-173. (Pubitemid 351735952)
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.1
, pp. 165-173
-
-
Bakkaloglu, B.1
O'Roak, B.J.2
Louvi, A.3
Gupta, A.R.4
Abelson, J.F.5
Morgan, T.M.6
Chawarska, K.7
Klin, A.8
Ercan-Sencicek, A.G.9
Stillman, A.A.10
Tanriover, G.11
Abrahams, B.S.12
Duvall, J.A.13
Robbins, E.M.14
Geschwind, D.H.15
Biederer, T.16
Gunel, M.17
Lifton, R.P.18
State, M.W.19
-
61
-
-
77950587223
-
Rare copy number variants: A point of rarity in genetic risk for bipolar disorder and schizophrenia
-
Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK et al. Rare copy number variants: A point of rarity in genetic risk for bipolar disorder and schizophrenia. Arch Gen Psychiatry 2010; 67: 318-327.
-
(2010)
Arch Gen Psychiatry
, vol.67
, pp. 318-327
-
-
Grozeva, D.1
Kirov, G.2
Ivanov, D.3
Jones, I.R.4
Jones, L.5
Green, E.K.6
-
62
-
-
67651160485
-
Meta-analysis of 32 genome-wide linkage studies of schizophrenia
-
Ng MY, Levinson DF, Faraone SV, Suarez BK, DeLisi LE, Arinami T et al. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry 2009; 14: 774-785.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 774-785
-
-
Ng, M.Y.1
Levinson, D.F.2
Faraone, S.V.3
Suarez, B.K.4
DeLisi, L.E.5
Arinami, T.6
-
63
-
-
0030726460
-
A gene spans the pseudoautosomal boundary in mice
-
DOI 10.1073/pnas.94.22.12030
-
Palmer S, Perry J, Kipling D, Ashworth A. A gene spans the pseudoautosomal boundary in mice. Proc Natl Acad Sci USA 1997; 94: 12030-12035. (Pubitemid 27467837)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.22
, pp. 12030-12035
-
-
Palmer, S.1
Perry, J.2
Kipling, D.3
Ashworth, A.4
-
64
-
-
6844261193
-
The mouse Mid1 gene: Implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
-
DOI 10.1093/hmg/7.3.489
-
Dal Zotto L, Quaderi NA, Elliott R, Lingerfelter PA, Carrel L, Valsecchi V et al. The mouse Mid1 gene: Implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Hum Mol Genet 1998; 7: 489-499. (Pubitemid 28120641)
-
(1998)
Human Molecular Genetics
, vol.7
, Issue.3
, pp. 489-499
-
-
Dal Zotto, L.1
Quaderi, N.A.2
Elliott, R.3
Lingerfelter, P.A.4
Carrel, L.5
Valsecchi, V.6
Montini, E.7
Yen, C.-H.8
Chapman, V.9
Kalcheva, I.10
Arrigo, G.11
Zuffardi, O.12
Thomas, S.13
Willard, H.F.14
Ballabio, A.15
Disteche, C.M.16
Rugarli, E.I.17
-
65
-
-
35649018206
-
Recurrent DNA copy number variation in the laboratory mouse
-
DOI 10.1038/ng.2007.19, PII NG200719
-
Egan CM, Sridhar S, Wigler M, Hall IM. Recurrent DNA copy number variation in the laboratory mouse. Nat Genet 2007; 39: 1384-1389. (Pubitemid 350034999)
-
(2007)
Nature Genetics
, vol.39
, Issue.11
, pp. 1384-1389
-
-
Egan, C.M.1
Sridhar, S.2
Wigler, M.3
Hall, I.M.4
-
66
-
-
42949106450
-
MID1 mutations in patients with X-linked Opitz G/BBB syndrome
-
DOI 10.1002/humu.20706
-
Fontanella B, Russolillo G, Meroni G. MID1 mutations in patients with X-linked Opitz G/BBB syndrome. Hum Mutat 2008; 29: 584-594. (Pubitemid 351614581)
-
(2008)
Human Mutation
, vol.29
, Issue.5
, pp. 584-594
-
-
Fontanella, B.1
Russolillo, G.2
Meroni, G.3
-
67
-
-
0034641894
-
New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome
-
Cox TC, Allen LR, Cox LL, Hopwood B, Goodwin B, Haan E et al. New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome. Hum Mol Genet 2000; 9: 2553-2562.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2553-2562
-
-
Cox, T.C.1
Allen, L.R.2
Cox, L.L.3
Hopwood, B.4
Goodwin, B.5
Haan, E.6
-
68
-
-
44349186162
-
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
-
Christian SL, Brune CW, Sudi J, Kumar RA, Liu S, Karamohamed S et al. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry 2008; 63: 1111-1117.
-
(2008)
Biol Psychiatry
, vol.63
, pp. 1111-1117
-
-
Christian, S.L.1
Brune, C.W.2
Sudi, J.3
Kumar, R.A.4
Liu, S.5
Karamohamed, S.6
-
69
-
-
0034303523
-
The origins, patterns and implications of human spontaneous mutation
-
Crow JF. The origins, patterns and implications of human spontaneous mutation. Nat Rev Genet 2000; 1: 40-47.
-
(2000)
Nat Rev Genet
, vol.1
, pp. 40-47
-
-
Crow, J.F.1
-
70
-
-
0029103381
-
Aneuploidies and micronuclei in the germ cells of male mice of advanced age
-
Lowe X, Collins B, Allen J, Titenko-Holland N, Breneman J, van Beek M et al. Aneuploidies and micronuclei in the germ cells of male mice of advanced age. Mutat Res 1995; 338: 59-76.
-
(1995)
Mutat Res
, vol.338
, pp. 59-76
-
-
Lowe, X.1
Collins, B.2
Allen, J.3
Titenko-Holland, N.4
Breneman, J.5
Van Beek, M.6
-
71
-
-
33645732369
-
Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man
-
Thomas NS, Durkie M, Van Zyl B, Sanford R, Potts G, Youings S et al. Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man. Hum Genet 2006; 119: 444-450.
-
(2006)
Hum Genet
, vol.119
, pp. 444-450
-
-
Thomas, N.S.1
Durkie, M.2
Van Zyl, B.3
Sanford, R.4
Potts, G.5
Youings, S.6
-
72
-
-
77349124038
-
De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age
-
Thomas NS, Morris JK, Baptista J, Ng BL, Crolla JA, Jacobs PA. De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age. J Med Genet 2010; 47: 112-115.
-
(2010)
J Med Genet
, vol.47
, pp. 112-115
-
-
Thomas, N.S.1
Morris, J.K.2
Baptista, J.3
Ng, B.L.4
Crolla, J.A.5
Jacobs, P.A.6
-
73
-
-
0142059634
-
The paternalage effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm
-
DOI 10.1086/378419
-
Glaser RL, Broman KW, Schulman RL, Eskenazi B, Wyrobek AJ, Jabs EW. The paternalage effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm. Am J Hum Genet 2003; 73: 939-947. (Pubitemid 37271895)
-
(2003)
American Journal of Human Genetics
, vol.73
, Issue.4
, pp. 939-947
-
-
Glaser, R.L.1
Broman, K.W.2
Schulman, R.L.3
Eskenazi, B.4
Wyrobek, A.J.5
Jabs, E.W.6
-
74
-
-
0242319701
-
Linear increase of structural and numerical chromosome 9 abnormalities in human sperm regarding age
-
DOI 10.1038/sj.ejhg.5201049
-
Bosch M, Rajmil O, Egozcue J, Templado C. Linear increase of structural and numerical chromosome 9 abnormalities in human sperm regarding age. Eur J Hum Genet 2003; 11: 754-759. (Pubitemid 37337058)
-
(2003)
European Journal of Human Genetics
, vol.11
, Issue.10
, pp. 754-759
-
-
Bosch, M.1
Rajmil, O.2
Egozcue, J.3
Templado, C.4
-
75
-
-
35648963256
-
Aberrant epigenetic regulation could explain the relationship of paternal age to schizophrenia
-
DOI 10.1093/schbul/sbm093
-
Perrin MC, Brown AS, Malaspina D. Aberrant epigenetic regulation could explain the relationship of paternal age to schizophrenia. Schizophr Bull 2007; 33: 1270-1273. (Pubitemid 350022778)
-
(2007)
Schizophrenia Bulletin
, vol.33
, Issue.6
, pp. 1270-1273
-
-
Perrin, M.C.1
Brown, A.S.2
Malaspina, D.3
-
76
-
-
33745175531
-
A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications
-
She X, Liu G, Ventura M, Zhao S, Misceo D, Roberto R et al. A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications. Genome Res 2006; 16: 576-583.
-
(2006)
Genome Res
, vol.16
, pp. 576-583
-
-
She, X.1
Liu, G.2
Ventura, M.3
Zhao, S.4
Misceo, D.5
Roberto, R.6
-
79
-
-
33845529974
-
The romance of balancing selection versus the sober alternatives: Let the data rule
-
DOI 10.1017/S0140525X06349096, PII S0140525X06349096
-
McGrath JJ. The romance of balancing selection versus the sober alternatives: Let the data rule (Commentary on Keller and Miller). Behav Brain Sci 2006; 29: 417-418. (Pubitemid 44921346)
-
(2006)
Behavioral and Brain Sciences
, vol.29
, Issue.4
, pp. 417-418
-
-
McGrath, J.J.1
|