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T.J.R. van de Pol

Observed names: T J van de Pol, T Van Den Pol, T. J. R. van de Pol, T. J. van de Pol, TJR van de Pol
OpenAlex ID: A5110008543
Isolation of a candidate gene for Norrie disease by positional cloning
1992 · W. Berger, A. Meindl, et al. · Nature Genetics · 253
Molecular basis of choroideremia (CHM): Mutations involving the rab escort protein-1 (REP-1) gene
1997 · JAJM van den Hurk, M Schwartz, et al. · Human Mutation · 173
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An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region
1987 · F. P. M. Cremers, R. A. Pfeiffer, et al. · Human Genetics · 81
Complete Exon–Intron Structure of the Retina-Specific ATP Binding Transporter Gene (ABCR) Allows the Identification of Novel Mutations Underlying Stargardt Disease
1998 · S. Gerber, J.M. Rozet, et al. · Genomics · 79
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing.
1992 · J A van den Hurk, T J van de Pol, et al. · Europe PMC (PubMed Central) · 62
Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.
1988 · F P Cremers, T J van de Pol, et al. · Europe PMC (PubMed Central) · 56
Deletion of the DXS165 locus in patients with classical Choroideremia
1987 · F.P.M. Cremers, F. Brunsmann, et al. · Clinical Genetics · 36
Genetic fine mapping of the gene for recessive Stargardt disease
1996 · C. B. Hoyng, F. Poppelaars, et al. · Human Genetics · 31
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Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs☆
2003 · M.W.J. Luijendijk, T.J.R. van de Pol, et al. · Genomics · 23
Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis
1990 · T.J.R. van de Pol, F.P.M. Cremers, et al. · Nucleic Acids Research · 19
Cloning of the breakpoints of a deletion associated with choroideremia
1990 · F. P. M. Cremers, F. Brunsmann, et al. · Human Genetics · 17
Yeast Artificial Chromosome Cloning of the Xq13.3-q21.31 Region and Fine Mapping of a Deletion Associated with Choroideremia and Nonspecific Mental Retardation
1995 · S.M. van der Maarel, I.H.J.M. Scholten, et al. · European Journal of Human Genetics · 16
Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome
1992 · W. Berger, A. Meindl, et al. · Human Genetics · 9
Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2
1992 · C.M. Molloy, T.J.R. van de Pol, et al. · Nucleic Acids Research · 5
Erratum: isolation of a candidate gene for Norrie disease by positional cloning. Nat Genet 2:84
1992 · Wilhelm Berger, A Meindl, et al. · 4
Molecular characterization of x linked deletions and duplications employing conventional southern analysis and long range restriction mapping
1987 · F.P.M. Cremers, P.J. Diergaarde, et al. · Cytogenetic and Genome Research
Works count: 16
Citation count: 864
H-index: 12
I10-index: 12
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