Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hamalainen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor R, Zwart J-A, Ilmavirta M, Havanka H, Farkkila M, Peltonen L, Palotie A A susceptibility locus for migraine with aura on chromosome 4q24.
American Journal of Human Genetics
2002;
70:
652-662.
Saarela J, Schoenberg Fejzo M, Chen D, Finnila S, Parkkonen M, Kuokkanen S, Sobel E, Tienari PJ, Sumelahti M-L, Wikstrom J, Elovaara I, Koivisto K, Pirttila T, Reunanen M, Palotie A, Peltonen L Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24.
Human Molecular Genetics
2002;
11:
2257-2267.
Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R, Suhonen J, Ellonen P, Chan G, Sinsheimer JS, Sobel E, Juvonen H, Arajarvi R, Partonen T, Suvisaari J, Lonnqvist J, Meyer J, Peltonen L Chromosome 1 loci in Finnish schizophrenia families..
Human Molecular Genetics
2001;
10:
1611-1617.
Sobel, E Sengul, H Weeks, DE Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees..
Human heredity. .
2001;
52(3):
121-31.
Magre J, Delpine M, Khallouf E, Gedde-Dahl T, Van Maldergem L, Sobel E, Papp J, Meier M, Mgarban A, BSCL Working Group, Lathrop M, Capeau J Mutations in the human homologue of GNG3LG cause Berardinelli-Seip congenital lipodystrophy linked to chromosome 11q13.
Nature Genetics
2001;
28:
365-370.
Sobel E, Weeks DE Haplotype analysis.
Encyclopedia of Biostatistics
1998;
3:
1804-1812.
Davis S, Sobel E, Marinov M, Weeks DE Analysis of bipolar disorder using affected relatives (Genetic Analysis Workshop 10: Detection of genes for complex traits).
Genetic Epidemiology
1997;
14:
605-610.
Sobel E, Lange K, O'Connell JR, Weeks DE Haplotyping algorithms.
Genetic mapping and DNA sequencing (IMA Volumes in Mathematics and its Applications)
1996;
81:
89-110.
Lange E, Gatti RA, Sobel E, Concannon P, Lange K How many ataxia-telangiectasia genes.
Ataxia-Telangiectasia (NATO ASI Series)
1993;
H77:
37-54.
Sobel E, Lange E, Jaspers NGJ, Chessa L, Sanal O, Shiloh Y, Taylor AMR, Weemaes CMA, Lange K, Gatti RA Ataxia-telangiectasia: linkage evidence for genetic heterogeneity.
American Journal of Human Genetics
1992;
50:
1343-1348.
Foroud T, Wei S, Ziv Y, Sobel E, Lange E, Chao A, Goradia T, Huo Y, Tolun A, Chessa L, Charmley P, Sanal O, Salman N, Julier C, Concannon P, McConville C, Taylor AMR, Shiloh Y, Lange K, Gatti RA Localization of an ataxia-telangiectasia locus to a 3 cM interval on chromosome 11q23: linkage analyses of 111 families by an international consortium.
American Journal of Human Genetics
1991;
49:
1263-1279.
Gatti RA, Lange E, Sobel E, Lange K Localization of the ataxia-telangiectasia gene(s) to a 3 cM interval on chromosome 11q23 by linkage analysis.
Cytogenetics and Cell Genetics
1991;
58:
1959-1960.
Barstow T, Cooper D, Sobel E, Landaw E, Epstein S Influence of increased metabolic rate on [13C] bicarbonate washout kinetics.
American Journal of Physiology
1990;
259:
R163-R171.
Sobel E, Martinez H A multiple sequence alignment program.
Nucleic Acids Research
1986;
14:
363-374.
Lange, K Sinsheimer, JS Sobel, E Association testing with Mendel..
Genetic epidemiology. .
2005;
29(1):
36-50.
Lilja, HE Suviolahti, E Soro-Paavonen, A Hiekkalinna, T Day, A Lange, K Sobel, E Taskinen, MR Peltonen, L Perola, M Pajukanta, P Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia..
Journal of lipid research. .
2004;
45(10):
1876-84.
Song, KK Weeks, DE Sobel, E Feingold, E Efficient simulation of P values for linkage analysis..
Genetic epidemiology. .
2004;
26(2):
88-96.
Keavney, B McKenzie, CA Connell, JM Julier, C Ratcliffe, PJ Sobel, E Lathrop, M Farrall, M Measured haplotype analysis of the angiotensin-I converting enzyme gene..
Human molecular genetics. .
1998;
7(11):
1745-51.
Sobel, E Lange, K Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics..
American journal of human genetics. .
1996;
58(6):
1323-37.
Lange, E Borresen, AL Chen, X Chessa, L Chiplunkar, S Concannon, P Dandekar, S Gerken, S Lange, K Liang, T Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium..
American journal of human genetics. .
1995;
57(1):
112-9.
Sanal, O Lange, E Telatar, M Sobel, E Salazar-Novak, J Ersoy, F Morrison, A Concannon, P Tolun, A Gatti, RA Ataxia-telangiectasia: linkage analysis of chromosome 11q22-23 markers in Turkish families..
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology. .
1992;
6(10):
2848-52.