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2p11
A chromosome band present on 2p
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosome 2 Short Arm
Chromosomes
FABP1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2011
Highly Cited
2011
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
Z. Kote-Jarai
,
Ali Amin Al Olama
,
+128 authors
R. Eeles
Nature Genetics
2011
Corpus ID: 205357914
Prostate cancer (PrCa) is the most frequently diagnosed male cancer in developed countries. We conducted a multi-stage genome…
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Highly Cited
2007
Highly Cited
2007
B Cell Lymphomas
Rita M. Braziel
,
Guang Fan
2007
Corpus ID: 73024915
The classification of malignant lymphoma has always been a controversial subject, well-reflected in Rupert Willis’ statement…
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Highly Cited
2005
Highly Cited
2005
Genome-wide array-based CGH for mantle cell lymphoma: identification of homozygous deletions of the proapoptotic gene BIM
H. Tagawa
,
S. Karnan
,
+6 authors
M. Seto
Oncogene
2005
Corpus ID: 18355603
Mantle cell lymphoma (MCL) is characterized by 11q13 chromosomal translocation and CCND1 overexpression, but additional genomic…
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2004
2004
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
M. Peyrard-Janvid
,
H. Anthoni
,
+8 authors
J. Kere
Human Genetics
2004
Corpus ID: 26215216
Developmental dyslexia, or reading disability, is a multigenic complex disease for which at least five loci, i.e. DYX1–3 and DYX5…
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Highly Cited
2003
Highly Cited
2003
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32
N. Kaminen
,
K. Hannula-Jouppi
,
+8 authors
J. Kere
Journal of medical genetics
2003
Corpus ID: 27351706
Developmental dyslexia is a distinct learning disability with unexpected difficulty in learning to read despite adequate…
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Highly Cited
2001
Highly Cited
2001
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.
I. Simonic
,
D. Nyholt
,
+5 authors
J. Weber
American journal of medical genetics
2001
Corpus ID: 28765295
Utilizing DNA samples from 91 Afrikaner nuclear families with one or more affected children, five genomic regions on chromosomes…
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Highly Cited
1998
Highly Cited
1998
Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma.
M. Chesi
,
P. L. Bergsagel
,
+6 authors
W. Kuehl
Blood
1998
Corpus ID: 14835515
Dysregulation of oncogenes by translocation to an IgH (14q32) or IgL (kappa, 2p11 or lambda, 22q11) locus is a frequent event in…
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Review
1998
Review
1998
Masquerading repeats: paralogous pitfalls of the human genome.
E. Eichler
Genome research
1998
Corpus ID: 38998632
In its most simple terms, the human genome consists of two distinct fractions of DNA: repetitive and unique sequence…
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Highly Cited
1993
Highly Cited
1993
Cytogenetic studies in splenic lymphoma with villous lymphocytes
D. Oscier
,
E. Matutes
,
+5 authors
D. Catovsky
British journal of haematology
1993
Corpus ID: 25715572
Summary. We report the cytogenetic findings on 31 cases of splenic lymphoma with villous lymphocytes (SLVL). TPA stimulated cells…
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Highly Cited
1984
Highly Cited
1984
Chromosome study of Ewing's sarcoma (ES) cell lines. Consistency of a reciprocal translocation t(11;22)(q24;q12).
C. Turc‐Carel
,
I. Philip
,
M. Berger
,
T. Philip
,
G. Lenoir
Cancer genetics and cytogenetics
1984
Corpus ID: 3397872
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