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ZNF41 gene
Known as:
MGC8941
, MRX89
, ZINC FINGER PROTEIN 41
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Verification of ZNF41 as a serum candidate biomarker for ventricular septal defect
Huang-Ming Hu
2014
Corpus ID: 76144237
Objective To validate zinc finger protein 41( ZNF41) as a serum candidate biomarker in patients with ventricular septal defect…
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2013
2013
Whole Genome Sequencing Analysis of an Idiopathic Intellectual Disability Syndrome
G. Lyon
,
Jason O'Rawe
,
+4 authors
J. Swensen
2013
Corpus ID: 81726858
We present a new idiopathic intellectual disability syndrome accompanied with distinctive facial dysmorphology. X-chromosome…
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2012
2012
335.4 kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features.
V. Alesi
,
M. Bértoli
,
+7 authors
G. Serra
Gene
2012
Corpus ID: 24743384
2010
2010
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation
D. Lugtenberg
,
L. Zangrande-Vieira
,
+27 authors
A. D. de Brouwer
American journal of medical genetics. Part A
2010
Corpus ID: 22958614
ZNF630 is a member of the primate‐specific Xp11 zinc finger gene cluster that consists of six closely related genes, of which…
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Review
2005
Review
2005
X linked mental retardation: a clinical guide
F. L. Raymond
Journal of Medical Genetics
2005
Corpus ID: 16313443
Mental retardation is more common in males than females in the population, assumed to be due to mutations on the X chromosome…
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2004
2004
Loss of functional ZNF41 in a female patient with a balanced translocation t(X;7)(p11.3;q11.21) and severe mental retardation: evidence for a role for ZNF41 in cognitive development
S. Shoichet
,
K. Hoffmann
,
+11 authors
V. Kalscheuer
2004
Corpus ID: 78659232
Highly Cited
2003
Highly Cited
2003
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
S. Shoichet
,
K. Hoffmann
,
+12 authors
V. Kalscheuer
American journal of human genetics
2003
Corpus ID: 22839077
Nonsyndromic X-linked mental retardation (MRX) is defined by an X-linked inheritance pattern of low IQ, problems with adaptive…
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1999
1999
Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41
M. Rosati
,
A. Franzè
,
M. R. Matarazzo
,
G. Grimaldi
Cytogenetic and Genome Research
1999
Corpus ID: 26777065
ZNF41 belongs to a cluster of human zinc finger genes residing within a gene-rich region at Xp11.23. ZNF41 encodes a KRAB/FPB (Kr…
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1994
1994
Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1.
J. Knight
,
G. Grimaldi
,
H. Thiesen
,
N. Bech-Hansen
,
C. Fletcher
,
M. Coleman
Genomics
1994
Corpus ID: 42691944
The ZNF21, ZNF41, and ZNF81 genes encode Krüppel-type zinc-finger proteins (ZFPs) and have previously been mapped to chromosome…
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1991
1991
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome.
A. Franzè
,
N. Archidiacono
,
M. Rocchi
,
M. Marino
,
G. Grimaldi
Genomics
1991
Corpus ID: 39439876
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