The Greig cephalopolysyndactyly syndrome

por Biesecker, Leslie G
Publicado 2008

An introduction to standardized clinical nomenclature for dysmorphic features: the Elements of Morphology project

por Biesecker, Leslie G
Publicado 2010

Polydactyly: How many disorders and how many genes: 2010 update

por Biesecker, Leslie G.
Publicado 2011

The New World of Clinical Genomics

por Biesecker, Leslie G.
Publicado 2012

Incidental Variants Are Critical for Genomics

por Biesecker, Leslie G.
Publicado 2013

Hypothesis-generating research and predictive medicine

por Biesecker, Leslie G.
Publicado 2013

Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: Lessons from the ClinSeq™ project

por Biesecker, Leslie G.
Publicado 2012

Secondary variants and human subjects research

por Biesecker, Leslie G.
Publicado 2013

Genomic screening for monogenic forms of diabetes

por Biesecker, Leslie G.
Publicado en BMC Med (2018)

Mosaic Disorders and the Taxonomy of Human Disease

por Biesecker, Leslie G.
Publicado en Genet Med (2017)

Genomic screening and genomic diagnostic testing—two very different kettles of fish

por Biesecker, Leslie G.
Publicado en Genome Med (2019)

Next Generation Sequencing Demands Next Generation Phenotyping

por Hennekam, Raoul CM, Biesecker, Leslie G
Publicado 2012

Databases of genomic variation and phenotypes: existing resources and future needs

por Johnston, Jennifer J., Biesecker, Leslie G.
Publicado 2013

An approach to pediatric exome and genome sequencing

por Biesecker, Leslie G., Biesecker, Barbara B.
Publicado en Curr Opin Pediatr (2014)

The ACMG/AMP reputable source criteria for the interpretation of sequence variants

por Biesecker, Leslie G., Harrison, Steven M.
Publicado en Genet Med (2018)

Prophylactic anticoagulation of individuals with Proteus syndrome and COVID-19

por Ours, Christopher A., Biesecker, Leslie G.
Publicado en Am J Med Genet A (2020)

SomatoSim: precision simulation of somatic single nucleotide variants

por Hawari, Marwan A., Hong, Celine S., Biesecker, Leslie G.
Publicado en BMC Bioinformatics (2021)

Exome sequencing: the expert view

por Biesecker, Leslie G, Shianna, Kevin V, Mullikin, Jim C
Publicado 2011

Reporting Genomic Sequencing Results to Ordering Clinicians: Incidental, but Not Exceptional

por Green, Robert C., Lupski, James R., Biesecker, Leslie G.
Publicado 2013

Systematic Evaluation of Sanger Validation of NextGen Sequencing Variants

por Beck, Tyler F., Mullikin, James C., Biesecker, Leslie G.
Publicado en Clin Chem (2016)