Citation Impact
Citing Papers
Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy
2010 StandoutScience
Genetic analysis of β-thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype
1997
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
2003 StandoutNature
The β-Thalassemias
1999 Standout
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
2007 StandoutNobel
Sickle Cell Anaemia
2002
Liver Adenosine Monophosphate-Activated Kinase-α2 Catalytic Subunit Is a Key Target for the Control of Hepatic Glucose Production by Adiponectin and Leptin But Not Insulin
2006
6 β-Thalassaemia
1993
HLA‐DR typing by PCR amplification with sequence‐specific primers (PCR‐SSP) in 2 hours: An alternative to serological DR typing in clinical practice including donor‐recipient matching in cadaveric transplantation
1992 Standout
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1991 StandoutNature
Maternal Uniparental Disomy of Chromosome 1 with Reduction to Homozygosity of the LAMB3 Locus in a Patient with Herlitz Junctional Epidermolysis Bullosa
1997
LACK OF EVIDENCE OF PERMANENT ENGRAFTMENT AFTER IN UTERO FETAL STEM CELL TRANSPLANTATION IN CONGENITAL HEMOGLOBINOPATHIES1
1996
8 The population genetics of the haemoglobinopathies
1993
Presence of fetal DNA in maternal plasma and serum
1997 Standout
Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes
1988
Gene Defects in β‐Thalassemia and Their Prenatal Diagnosis
1990
Sickle-cell disease
2010 Standout
Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Parent-Specific Methylation in Fetuses
1997
Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis
1998 Standout
Mycotoxins and human disease: a largely ignored global health issue
2009 Standout
What We Talk About When We Talk About Fat
2014 Standout
Global epidemiology of haemoglobin disorders and derived service indicators
2008 Standout
World distribution of factor V Leiden
1995 Standout
Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
1996
Energy Metabolism in the Liver
2014 Standout
Cytochrome P450 enzymes in drug metabolism: Regulation of gene expression, enzyme activities, and impact of genetic variation
2013 Standout
Genomic imprinting: parental influence on the genome
2001 Standout
Why are some genetic diseases common?
1993
Growth effects of uniparental disomies and the conflict theory of genomic imprinting
1997
HLA‐DRB101 subtyping by allele‐specific PCR amplification: A sensitive, specific and rapid technique
1991
Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?
1998
Strategy linking several analytical methods of neonatal screening for sickle cell disease
2001
A Common Human β Globin Splicing Mutation Modeled in Mice
1998 StandoutNobel
Molecular basis and prenatal diagnosis of beta-thalassemia
1988
Dominant Contribution of P450 3A4 to the Hepatic Carcinogenic Activation of Aflatoxin B1
2006
Review: Leptin gene expression in the placenta – Regulation of a key hormone in trophoblast proliferation and survival
2011
Works of FF Chehab being referenced
Is Hb A2Elevated in Adults with Sickle-A-Thalassemi (βS/βS; -α/-α)
1997
Detection of sickle cell anaemia mutation by colour DNA amplification
1990
The Use of Animal Models to Dissect the Biology of Leptin
2004
Characterization of a spontaneous mutation in beta-thalassemia associated with advanced paternal age
1989
Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.
1994
The molecular basis of beta-thalassemia in Lebanon: application to prenatal diagnosis
1987
Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily
1993