-
2
-
-
0028359950
-
A case-control family history study of autism
-
(1994)
J. Child Psychol. Psychiatry
, vol.35
, pp. 877-900
-
-
Bolton, P.1
Macdonald, H.2
Pickles, A.3
Rios, P.4
Goode, S.5
Crowson, M.6
Bailey, A.7
Rutter, M.8
-
3
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
(1989)
J. Child Psychol. Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenberg, S.1
Gillberg, C.2
Hellgre, L.3
Anderen, L.4
Gillberg, I.5
Jackobsson, G.6
Bohman, M.7
-
4
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 571-578
-
-
-
5
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
-
6
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nouri, N.4
Hinds, D.5
Hallmayer, J.6
Kalaydjieva, L.7
McCague, P.8
Dimiceli, S.9
Pitts, T.10
-
7
-
-
0033573212
-
An autosomal genomic screen for autism. Collaborative linkage study of autism
-
(1999)
Am. J. Med. Genet.
, vol.88
, pp. 609-615
-
-
Barrett, S.1
Beck, J.C.2
Bernier, R.3
Bisson, E.4
Braun, T.A.5
Casavant, T.L.6
Childress, D.7
Folstein, S.E.8
Garcia, M.9
Gardiner, M.B.10
-
8
-
-
0032729834
-
Genetic studies of autistic disorder and chromosome 7
-
(1999)
Genomics
, vol.61
, pp. 227-236
-
-
Ashley-Koch, A.1
Wolpert, C.M.2
Menold, M.M.3
Zaeem, L.4
Basu, S.5
Donnelly, S.L.6
Ravan, S.A.7
Powell, C.M.8
Qumsiyeh, M.B.9
Aylsworth, A.S.10
-
12
-
-
0033802632
-
The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
-
(2000)
J. Autism Dev. Disord.
, vol.30
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
Cook E.H., Jr.4
Leventhal, B.L.5
DiLavore, P.C.6
Pickles, A.7
Rutter, M.8
-
16
-
-
0028832203
-
Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1221-1232
-
-
Holmans, P.1
Clayton, D.2
-
18
-
-
0032870497
-
Exploring the dense mapping of a region of potential linkage in complex disease: An example in multiple sclerosis
-
(1999)
Genet. Epidemiol.
, vol.17
, pp. 51-63
-
-
Feakes, R.1
Sawcer, S.2
Chataway, J.3
Coraddu, F.4
Broadley, S.5
Gray, J.6
Jones, H.B.7
Clayton, D.8
Goodfellow, P.N.9
Compston, A.10
-
23
-
-
0004998039
-
-
Arlequin Version 2.000: A Software for Population Genetics Data Analysis. Genetics and Biometry Laboratory, University of Geneva, Switzerland.
-
(2000)
-
-
Schneider, S.1
Roessli, D.2
Excoffier, L.3
-
27
-
-
0030947270
-
Human PEG1/MEST, an imprinted gene on chromosome 7
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 781-786
-
-
Kobayashi, S.1
Kohda, T.2
Miyoshi, N.3
Kuroiwa, Y.4
Aisaka, K.5
Tsutsumi, O.6
Kaneko-Ishino, T.7
Ishino, F.8
-
29
-
-
0034702031
-
Evaluation of fine mapping strategies for a multifactorial disease locus: Systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1291-1301
-
-
Herr, M.1
Dudbridge, F.2
Zavattari, P.3
Cucca, F.4
Guja, C.5
March, R.6
Campbell, R.D.7
Barnett, A.H.8
Bain, S.C.9
Todd, J.A.10
Koeleman, B.P.11
-
30
-
-
0033927713
-
Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1833-1844
-
-
Nair, R.P.1
Stuart, P.2
Henseler, T.3
Jenisch, S.4
Chia, N.V.5
Westphal, E.6
Schork, N.J.7
Kim, J.8
Lim, H.W.9
Christophers, E.10
-
32
-
-
0033930144
-
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28
-
(2000)
Nature Genet.
, vol.25
, pp. 324-328
-
-
Taillon-Miller, P.1
Bauer-Sardina, I.2
Saccone, N.L.3
Putzel, J.4
Laitinen, T.5
Cao, A.6
Kere, J.7
Pilia, G.8
Rice, J.P.9
Kwok, P.Y.10
-
33
-
-
0033863391
-
SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 383-394
-
-
Martin, E.R.1
Lai, E.H.2
Gilbert, J.R.3
Rogala, A.R.4
Afshari, A.J.5
Riley, J.6
Finch, K.L.7
Stevens, J.F.8
Livak, K.J.9
Slotterbeck, B.D.10
-
34
-
-
0033574303
-
Drug firms to create public database of genetic mutations
-
(1999)
Science
, vol.284
, pp. 406-407
-
-
Marshall, E.1
-
35
-
-
0033865944
-
The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 357-368
-
-
Lai, C.S.1
Fisher, S.E.2
Hurst, J.A.3
Levy, E.R.4
Hodgson, S.5
Fox, M.6
Jeremiah, S.7
Povey, S.8
Jamison, D.C.9
Green, E.D.10
-
41
-
-
1842288542
-
Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients
-
(1997)
Hum. Genet.
, vol.100
, pp. 224-229
-
-
Klauck, S.M.1
Munstermann, E.2
Bieber-Martig, B.3
Ruhl, D.4
Lisch, S.5
Schmotzer, G.6
Poustka, A.7
Poustka, F.8
-
43
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5, 264 microsatellites
-
(1996)
Nature
, vol.380
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
-
44
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier Haddema, T.5
Manion, F.6
Quillen, J.7
Sheffield, V.C.8
Sunden, S.9
Duyk, G.M.10
-
45
-
-
0030819029
-
A physical map of human chromosome 7: An integrated YAC contig map with average STS spacing of 79 kb
-
(1997)
Genome Res.
, vol.7
, pp. 673-692
-
-
Bouffard, G.G.1
Idol, J.R.2
Braden, V.V.3
Iyer, L.M.4
Cunningham, A.F.5
Weintraub, L.A.6
Touchman, J.W.7
Mohr-Tidwell, R.M.8
Peluso, D.C.9
Fulton, R.S.10
-
46
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
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