Citation Impact
Citing Papers
Chromosome Abnormalities and Genetic Counseling
2011
Association Among Polymorphisms at MYH9 , Environmental Factors, and Nonsyndromic Orofacial Clefts in Western China
2009
Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch
2006
The Neurovascular Unit Coming of Age: A Journey through Neurovascular Coupling in Health and Disease
2017 Standout
MTHFRandMSX1contribute to the risk of nonsyndromic cleft lip/palate
2010
Association between the Transforming Growth Factor Alpha Gene and Nonsyndromic Oral Clefts: A HuGE Review
2006
Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate
2005
Be on Target: Strategies of Targeting Alternative and Lectin Pathway Components in Complement-Mediated Diseases
2018
Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders
2018 Standout
Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID-19 infection: A report of five cases
2020 Standout
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease
2002 Standout
Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2
2003
Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results
2009
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
2001
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Tissue Origins and Interactions in the Mammalian Skull Vault
2002 Standout
Cleft lip and palate
2009 Standout
NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
2005
Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes
2005
Analysis of the brain mural cell transcriptome
2016
Drug repurposing: progress, challenges and recommendations
2018 Standout
Genetic regulation of gene expression in the epileptic human hippocampus
2017
Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer
2007 Standout
Addressing the challenges of cleft lip and palate research in India
2009
Gene/environment causes of cleft lip and/or palate
2002
TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome
2008
Genetics of craniofacial development and malformation
2001
Molecular diagnosis of neurofibromatosis type 1: 2 years experience
2006
Health Supervision for Children With Down Syndrome
2011 Standout
Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking
2006 StandoutNobel
Mixed clefting type in Rapp‐Hodgkin syndrome
2002
CRISPLD2: a novel NSCLP candidate gene
2007
Variation in IRF6 contributes to nonsyndromic cleft lip and palate
2005
GREAT improves functional interpretation of cis-regulatory regions
2010 Standout
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate
2008
Guidelines for the diagnosis and management of individuals with neurofibromatosis 1
2006 Standout
Germline Missense Mutations Affecting KRAS Isoform B Are Associated with a Severe Noonan Syndrome Phenotype
2006
An update on the aetiology of orofacial clefts.
2004
Phosphate Transporters and Their Function
2013
CRISPLD2 Variants Including a C471T Silent Mutation May Contribute to Nonsyndromic Cleft Lip with or without Cleft Palate
2010
Renal Control of Calcium, Phosphate, and Magnesium Homeostasis
2014 Standout
Works of Melissa Lees being referenced
Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype
2011
COLEC10 is mutated in 3MC patients and regulates early craniofacial development
2017
Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome
2011
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities
2005
Different mutations in theNF1gene are associated with Neurofibromatosis–Noonan syndrome (NFNS)
2003
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs
2000
Novel de novo EEF 1A2 missense mutations causing epilepsy and intellectual disability
2016
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32
1999