DOI: 10.1086/377158. Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

10.1086/377158

Crossref journal-article

Elsevier BV

The American Journal of Human Genetics (78)

Bibliography

Sapp, P. C., Hosler, B. A., McKenna-Yasek, D., Chin, W., Gann, A., Genise, H., Gorenstein, J., Huang, M., Sailer, W., Scheffler, M., Valesky, M., Haines, J. L., Pericak-Vance, M., Siddique, T., Horvitz, H. R., & Brown, R. H. (2003). Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis. The American Journal of Human Genetics, 73(2), 397â403.

Authors 16

Peter C. Sapp (first)
Betsy A. Hosler (additional)
Diane McKenna-Yasek (additional)
Wendy Chin (additional)
Amity Gann (additional)
Hilary Genise (additional)
Julie Gorenstein (additional)
Michael Huang (additional)
Wen Sailer (additional)
Meg Scheffler (additional)
Marianne Valesky (additional)
Jonathan L. Haines (additional)
Margaret Pericak-Vance (additional)
Teepu Siddique (additional)
H. Robert Horvitz (additional)
Robert H. Brown (additional)

References 17 Referenced 98

10.1016/0022-510X(94)90191-0 / J Neurol Sci / El Escorial world federation of neurology criteria for the diagnosis of amyotrophic lateral sclerosis by Brooks (1994)
10.1126/science.8209258 / Science / Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation by Gurney (1994)
10.1038/ng1001-166 / Nat Genet / A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 by Hadano (2001)
10.1086/337945 / Am J Hum Genet / A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q by Hand (2002)
10.1001/jama.284.13.1664 / JAMA / Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 by Hosler (2000)
10.1073/pnas.032539299 / Proc Natl Acad Sci USA / Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS) by Howland (2002)
10.1073/pnas.81.11.3443 / Proc Natl Acad Sci USA / Strategies for multilocus linkage analysis in humans by Lathrop (1984)
10.1002/gepi.1370030105 / Genet Epidemiol / Construction of human linkage maps: likelihood calculations for multilocus linkage analysis by Lathrop (1986)
10.1523/JNEUROSCI.21-23-09246.2001 / J Neurosci / Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease by Nagai (2001)
{'key': '10.1086/377158_bib20', 'first-page': '543', 'article-title': 'Estimating the power of a proposed linkage study for a complex genetic trait', 'volume': '44', 'author': 'Ploughman', 'year': '1989', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / Estimating the power of a proposed linkage study for a complex genetic trait by Ploughman (1989)
10.1038/ng1123 / Nat Genet / Mutant dynactin in motor neuron disease by Puls (2003)
10.1073/pnas.92.3.689 / Proc Natl Acad Sci USA / Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis by Ripps (1995)
10.1038/362059a0 / Nature / Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis by Rosen (1993)
{'key': '10.1086/377158_bib24', 'article-title': 'X-linked dominant locus for late-onset familial amyotrophic lateral sclerosis', 'volume': 'A308', 'author': 'Siddique', 'year': '1998', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / X-linked dominant locus for late-onset familial amyotrophic lateral sclerosis by Siddique (1998)
{'key': '10.1086/377158_bib25', 'first-page': '1323', 'article-title': 'Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics', 'volume': '58', 'author': 'Sobel', 'year': '1996', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics by Sobel (1996)
10.1016/0896-6273(95)90259-7 / Neuron / An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria by Wong (1995)
10.1038/ng1001-160 / Nat Genet / The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis by Yang (2001)

Dates

Type	When
Created	22 years, 1 month ago (July 28, 2003, 4:57 p.m.)
Deposited	5 years, 5 months ago (March 24, 2020, 4:44 p.m.)
Indexed	3 weeks, 3 days ago (Aug. 7, 2025, 4:53 a.m.)
Issued	22 years, 1 month ago (Aug. 1, 2003)
Published	22 years, 1 month ago (Aug. 1, 2003)
Published Print	22 years, 1 month ago (Aug. 1, 2003)

Funders 0

None

BibTeX

@article{Sapp_2003, title={Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis}, volume={73}, ISSN={0002-9297}, url={http://dx.doi.org/10.1086/377158}, DOI={10.1086/377158}, number={2}, journal={The American Journal of Human Genetics}, publisher={Elsevier BV}, author={Sapp, Peter C. and Hosler, Betsy A. and McKenna-Yasek, Diane and Chin, Wendy and Gann, Amity and Genise, Hilary and Gorenstein, Julie and Huang, Michael and Sailer, Wen and Scheffler, Meg and Valesky, Marianne and Haines, Jonathan L. and Pericak-Vance, Margaret and Siddique, Teepu and Horvitz, H. Robert and Brown, Robert H.}, year={2003}, month=aug, pages={397–403} }

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