Clesson Turner - Concepedia

Author

Clesson Turner

Walter Reed National Military Medical Center ORCID

Also Known As

C Turner, C. TURNER, C. Turner, C.E. Turner, Clesson E. Turner, Clesson E Turner, Clesson E. Turner, Clesson Turner

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Walter Reed National Military Medical Center National Institutes of Health Wessex Regional Genetics Laboratory National Cancer Institute Uniformed Services University of the Health Sciences

About

Clesson Turner is an author at Walter Reed National Military Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	558
2	Engineering	1	1	33
3	Natural Sciences	1	1	146
4	Social Sciences	1	1	69
5	Cell Biology	1	1	45

Clesson Turner

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine Leslie G. Biesecker, James C. Mullikin, Flavia M. Facio, Genome Research	2009	260
Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer Clesson Turner, Christina Killoran, Nick Thomas, Human Genetics Genetic DiseasesMitochondrial TransplantationMitochondrial FunctionGenetic DisorderNatural Sciences	2003	146
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome Jung‐Hyun Kim, Deepali N. Shinde, Margot R.F. Reijnders, The American Journal of Human Genetics Developmental BiologyMendelian DisorderBrain DevelopmentGenetic DisorderGenetics	2016	111
Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotype Clesson Turner, N R Dennis, D. H. Skuse, Human Genetics	2000	108
<i>EIF2S3</i>Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO Martina Škopková, Friederike Hennig, Byung‐Sik Shin, Human Mutation GeneticsDisease Gene IdentificationTranscriptional RegulationMendelian DisorderTranslational Biology	2017	81
Frequent inactivating germline mutations in DNA repair genes in patients with Ewing sarcoma Andrew S. Brohl, Rajesh Patidar, Clesson Turner, Genetics in Medicine	2017	80
Proteogenomic analysis of lung adenocarcinoma reveals tumor heterogeneity, survival determinants, and therapeutically relevant pathways Anthony R. Soltis, Nicholas W. Bateman, Jianfang Liu, Cell Reports Medicine	2022	74
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia Hanneke A. Haijes, Maria J.E. Koster, Holger Rehmann, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental AnomalyDevelopmental BiologyMendelian DisorderBrain Development	2019	69
Whole-exome sequencing reveals germline-mutated small cell lung cancer subtype with favorable response to DNA repair–targeted therapies Camille Tlemsani, Nobuyuki Takahashi, Lőrinc Sándor Pongor, Science Translational Medicine	2021	69
Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes Matthew G. Rees, David Ng, Sarah L. Ruppert, Journal of Clinical Investigation GeneticsGenetic EpidemiologyGenetic ContributionPathologyGlucose Homeostasis	2011	45

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