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2q31-q33
A chromosome band present on 2q
National Institutes of Health
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1 relation
Chromosomes
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Lack of association between autism and SLC25A12.
R. Rabionet
,
J. McCauley
,
+10 authors
M. Pericak-Vance
The American journal of psychiatry
2006
Corpus ID: 36805651
OBJECTIVE Autism has a strong, complex genetic component, most likely involving several genes. Multiple genomic screens have…
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Highly Cited
2005
Highly Cited
2005
Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.
P. Concannon
,
H. Erlich
,
+5 authors
S. Rich
Diabetes
2005
Corpus ID: 17480993
Type 1 diabetes is a common, multifactorial disease with strong familial clustering (genetic risk ratio [lambda(S)] approximately…
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2004
2004
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes
R. Rabionet
,
J. Jaworski
,
+9 authors
M. Pericak-Vance
Neuroscience Letters
2004
Corpus ID: 18711012
Highly Cited
2002
Highly Cited
2002
ORMDL proteins are a conserved new family of endoplasmic reticulum membrane proteins
L. Hjelmqvist
,
M. Tuson
,
G. Marfany
,
Enric Herrero
,
S. Balcells
,
R. Gonzàlez-Duarte
Genome Biology
2002
Corpus ID: 1716711
BackgroundAnnotations of completely sequenced genomes reveal that nearly half of the genes identified are of unknown function…
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Highly Cited
2000
Highly Cited
2000
Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33.
Z. Deng
,
F. Haghighi
,
+6 authors
J. Knowles
American journal of respiratory and critical care…
2000
Corpus ID: 10465089
Familial primary pulmonary hypertension (PPH) is a rare autosomal dominant disease characterized by distinctive changes in…
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2000
2000
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.
R. Machado
,
M. Pauciulo
,
+7 authors
W. Nichols
Genomics
2000
Corpus ID: 23061114
Primary pulmonary hypertension (PPH), an often fatal disorder, is characterized by sustained elevation of pulmonary artery…
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Highly Cited
1999
Highly Cited
1999
The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.
B. Vaidya
,
H. Imrie
,
+8 authors
S. Pearce
Human molecular genetics
1999
Corpus ID: 30793458
Graves' disease (GD) is an autoimmune thyroid disorder that is inherited as a complex trait. We have genotyped 77 affected sib…
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Review
1998
Review
1998
DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.
S. Knuutila
,
A. Björkqvist
,
+12 authors
Y. Zhu
The American journal of pathology
1998
Corpus ID: 25894782
This review summarizes reports of recurrent DNA sequence copy number amplifications in human neoplasms detected by comparative…
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1998
1998
A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.
M. Bayés
,
B. Goldaracena
,
+10 authors
D. Grinberg
Journal of medical genetics
1998
Corpus ID: 36224740
Autosomal recessive retinitis pigmentosa (ARRP) is a genetically heterogeneous disease. To date, mutations in four members of the…
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Highly Cited
1996
Highly Cited
1996
Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8.
D. Luo
,
R. Buzzetti
,
+7 authors
J. She
Human molecular genetics
1996
Corpus ID: 14222210
Previous genome-wide mapping studies have provided suggestive linkage evidence for several novel susceptibility loci responsible…
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