Christine J. Shaw - Concepedia

Concepedia

Author

Christine J. Shaw

Texas Children's Hospital

Also Known As

Christine J. Shaw, Christine Shaw, Christine J. Shaw

15

Publications

1.3K

Citations

14

H-Index

36

Concepts

All Affiliations

Texas Children's Hospital Baylor College of Medicine Radboud University Medical Center La Roche College Radboud University Nijmegen

CJ

About

Christine J. Shaw is an author at Texas Children's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1K
2	Natural Sciences	4	4	424
3	Public Health	1	1	119
4	Biostatistics	1	1	119
5	Immunology	1	1	97

Christine J. Shaw

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15

Publications

1.3K

Citations

14

H-Index

	Year	Citations
Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements Paweł Stankiewicz, Christine J. Shaw, Jason Dapper, The American Journal of Human Genetics ChromatinNatural SciencesGeneticsGenome StructureDna Replication	2003	185
Structure and Evolution of the Smith-Magenis Syndrome Repeat Gene Clusters, SMS-REPs Sung Sup Park, Paweł Stankiewicz, Weimin Bi, Genome Research	2002	124
Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 Weimin Bi, Sung Sup Park, Christine J. Shaw, The American Journal of Human Genetics ChromatinGenome InstabilityGeneticsMolecular BiologyChromosome Biology	2003	123
Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing Joep de Ligt, Philip M. Boone, Rolph Pfundt, Human Mutation SequencingFunctional GenomicsMedicineGeneticsNext-generation Sequencing	2013	119
Serial segmental duplications during primate evolution result in complex human genome architecture Paweł Stankiewicz, Christine J. Shaw, Marjorie Withers, Genome Research	2004	115
Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)] Lorraine Potocki, Christine J. Shaw, Paweł Stankiewicz, Genetics in Medicine Genetic DisorderGeneticsHematologyGenetic EpidemiologyPathology	2003	113
Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms Christine J. Shaw, James R. Lupski Human Genetics Natural SciencesGeneticsGenomic MechanismDna ReplicationMolecular Biology	2004	112
Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome Weimin Bi, Gulam Mustafa Saifi, Christine J. Shaw, Human Genetics Phd-containing ProteinDisease MechanismMendelian DisorderGenetic DisorderNondeletion Patients	2004	111
Genetic Proof of Unequal Meiotic Crossovers in Reciprocal Deletion and Duplication of 17p11.2 Christine J. Shaw, Weimin Bi, James R. Lupski The American Journal of Human Genetics Reciprocal DeletionLinkage DisequilibriumUnequal Meiotic CrossoversGeneticsEvolutionary Biology	2002	98
The Alu-Rich Genomic Architecture of SPAST Predisposes to Diverse and Functionally Distinct Disease-Associated CNV Alleles Philip M. Boone, Bo Yuan, Ian M. Campbell, The American Journal of Human Genetics Allelic VariantNeurogenomicsGeneticsPathogenesisImmunology	2014	97

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