Citation Impact
Citing Papers
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
2010
Non-Invasive Prenatal Diagnosis of Multiple Endocrine Neoplasia Type 2A Using COLD-PCR Combined with HRM Genotyping Analysis from Maternal Serum
2012
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline
2016 Standout
Diagnosis and Treatment of Polycystic Ovary Syndrome: An Endocrine Society Clinical Practice Guideline
2013 Standout
Cell-free nucleic acids as biomarkers in cancer patients
2011 Standout
The obstetric and gynaecological management of women with inherited bleeding disorders – review with guidelines produced by a taskforce of UK Haemophilia Centre Doctors’ Organization
2006
Circulating Nucleic Acids in Plasma and Serum
2008
Liquid biopsies come of age: towards implementation of circulating tumour DNA
2017 Standout
Pregnancy in carriers of haemophilia
2007
Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy
2005
From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges
2012
High Resolution Size Analysis of Fetal DNA in the Urine of Pregnant Women by Paired-End Massively Parallel Sequencing
2012
Down syndrome
2020 Standout
The Diagnosis of Polycystic Ovary Syndrome during Adolescence
2015 Standout
Non-invasive tool for foetal sex determination in early gestational age
2011
Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma
2015 Standout
Quantitative Analysis of the Transrenal Excretion of Circulating EBV DNA in Nasopharyngeal Carcinoma Patients
2008
The tomato Dwarf gene isolated by heterologous transposon tagging encodes the first member of a new cytochrome P450 family.
1996
A Rice Brassinosteroid-Deficient Mutant, ebisu dwarf (d2), Is Caused by a Loss of Function of a New Member of Cytochrome P450
2003 Standout
Role of CD47 as a Marker of Self on Red Blood Cells
2000 StandoutScience
Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline
2018
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
The Rh blood group system: a review
2000
Preterm labor: One syndrome, many causes
2014 StandoutScience
Guidelines for the management of hemophilia
2012 Standout
WFH Guidelines for the Management of Hemophilia, 3rd edition
2020 Standout
Works of K. Finning being referenced
Non-invasive prenatal determination of fetal sex: translating research into clinical practice
2010
Early detection of cell-free fetal DNA in maternal plasma
2007
The Serological Profile and Molecular Basis of a New Partial D Phenotype, DHR
1997
Non‐invasive first trimester determination of fetal gender: a new approach for prenatal diagnosis of haemophilia
2006
Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetalRHDgenotyping service
2002
Molecular biology of partial D phenotypes
1996
Detection of cell-free fetal DNA in maternal urine
2006