C. Zuppi

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Aliases
C Zuppi, C. Zuppi, Cecilia Zuppi
Publication record
205 papers · 4,881 citations · H-index 35

PAPERS

A STARD-compliant prediction model for diagnosing thrombotic microangiopathies
20181 citationsauthor #5
Seminal suPAR Levels as Marker of Abacterial Male Accessory Gland Inflammation in Hypogonadism.
20184 citationsauthor #7
Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome
201718 citationsauthor #8
Identification and Characterization of a New BRCA2 Rearrangement in an Italian Family with Hereditary Breast and Ovarian Cancer Syndrome
20170 citationsauthor #8
CYP21A2 intronic variants causing 21-hydroxylase deficiency.
201716 citationsauthor #5
Comparison of Fully Automated and Semiautomated Systems for Protein Immunofixation Electrophoresis
20177 citationsauthor #6
Competitive PCR-High Resolution Melting Analysis (C-PCR-HRMA) for large genomic rearrangements (LGRs) detection: A new approach to assess quantitative status of BRCA1 gene in a reference laboratory.
201717 citationsauthor #10
Fecal but not serum calprotectin is a potential marker of GVHD after stem cell transplantation
201710 citationsauthor #6
UGT1A1 Polymorphism and Mortality Outcome after Allogeneic Stem CellTransplantation with Busulfan Based Regimen
20170 citationsauthor #7
Enhanced Liver Fibrosis Test as a Reliable Tool for Assessing Fibrosis in Nonalcoholic Fatty Liver Disease in a Clinical Setting
201734 citationsauthor #11
Identification and Characterization of a New BRCA2 Rearrangement in an Italian Family with Hereditary Breast and Ovarian Cancer Syndrome
201712 citationsauthor #8
Prevalence of alcohol and other drugs in injured drivers and their association with clinical outcomes.
201713 citationsauthor #7
ANNALS EXPRESS: Stimulating TSH receptor autoantibodies immunoassay: analytical evaluation and clinical performance in Graves' Disease.
201724 citationsauthor #5
Intraoperative high-dose calcium stimulation test in patients with sporadic medullary thyroid carcinoma is highly accurate in predicting lateral neck metastases.
20167 citationsauthor #5
Simultaneous quantification of 17-hydroxyprogesterone, androstenedione, testosterone and cortisol in human serum by LC-MS/MS using TurboFlow online sample extraction.
20169 citationsauthor #6
Urinary Albumin Detection: Comparison of Two Different Methods
20168 citationsauthor #6
Clinical and microbiological outcome in septic patients with extremely low 25-hydroxyvitamin D levels at initiation of critical care.
201645 citationsauthor #10
Evaluation of screening method for Bence Jones protein analysis
20163 citationsauthor #9
Validation of an LC-MS/MS Method for Urinary Lactulose and Mannitol Quantification: Results in Patients with Irritable Bowel Syndrome
201620 citationsauthor #9
Follow-up of IgD-κ multiple myeloma by monitoring free light chains and total heavy chain IgD: A case report
20162 citationsauthor #5
Role of Fourier transform infrared (FT-IR) spectroscopy in the evaluation of urinary stone disease
20160 citationsauthor #5
Pre-analytical phase in cryoglobulin (CRG) detection: an alternative method for sample transport
201615 citationsauthor #6
P1035 : ELF test is a reliable non invasive test for fibrosis in NAFLD subjects
20151 citationsauthor #9
Clinical outcome of septic patients with undetectable vitamin D levels at ICU admission
20150 citationsauthor #11
Soluble urokinase‐type plasminogen activator receptor as a putative marker of male accessory gland inflammation
201511 citationsauthor #7
Lactose intolerance genetic testing: is it useful as routine screening? Results on 1426 south-central Italy patients.
201534 citationsauthor #8
ELF TEST IS A RELIABLE TOOL FOR NON-INVASIVE DIAGNOSIS OF LIVER FIBROSIS IN PATIENTS WITH NONALCOHOLIC FATTY LIVER DISEASE
20150 citationsauthor #12
Nasal lavage levels of granulocyte‐macrophage colony‐stimulating factor and chronic nasal hypereosinophilia
201537 citationsauthor #13
Analytical evaluation of a new liquid immunoturbidimetric assay for the determination of ferritin in serum
20153 citationsauthor #6
A preliminary Quality Control (QC) for next generation sequencing (NGS) library evaluation turns out to be a very useful tool for a rapid detection of BRCA1/2 deleterious mutations.
201415 citationsauthor #8
FT-IR Analysis of Urinary Stones: A Helpful Tool for Clinician Comparison with the Chemical Spot Test
201437 citationsauthor #8
DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism.
201411 citationsauthor #7
Nasal fluid release of eotaxin‐3 and eotaxin‐2 in persistent sinonasal eosinophilic inflammation
201437 citationsauthor #11
Evaluation of the diagnostic and predictive power of PCA3 in the prostate cancer. A different best cut-off in each different scenario. Preliminary results.
20147 citationsauthor #5
Is Intraoperative Calcitonin Monitoring Useful to Modulate the Extension of Neck Dissection in Patients With Medullary Thyroid Carcinoma?
20145 citationsauthor #5
Analytical performance of the new analyzer BA 400 Biosystems with LED technology.
20143 citationsauthor #6
PCA3 score of 20 could improve prostate cancer detection: results obtained on 734 Italian individuals.
201426 citationsauthor #13
Falsely increased free triiodothyronine values in a woman affected by thyroiditis and multinodular goiter
20140 citationsauthor #4
Myocardial performance index and biochemical markers for early detection of doxorubicin-induced cardiotoxicity in children with acute lymphoblastic leukaemia
201355 citationsauthor #8
Circulating tumor cells in colorectal cancer patients.
201351 citationsauthor #6
Effects of prednisone on biomarkers of tubular damage induced by radiocontrast in interventional cardiology.
20139 citationsauthor #6
FETAL URINE ANALYSIS TO PREDICT POORPOSTNATAL FUNCTION IN TWO CASES OFCONGENITAL URINARY OBSTRUCTION
20130 citationsauthor #6
Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia.
20133 citationsauthor #6
Potential usefulness of CTC detection in follow up of prostate cancer patients. A preliminary report obtained by using Adnagene platform.
20137 citationsauthor #4
Small amplicons high resolution melting analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population.
20133 citationsauthor #4
Effects of lutein supplementation on biological antioxidant status in preterm infants: a randomized clinical trial
201321 citationsauthor #7
Total 25-Hydroxyvitamin D Determination by an Entry Level Triple Quadrupole Instrument: Comparison between Two Commercial Kits
20137 citationsauthor #3
Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
201378 citationsauthor #3
The First Case of Association Between Postpartum Thyroiditis and Thyroid Hormone Resistance in an Italian Patient Showing a Novel p.V283A THRB Mutation
20138 citationsauthor #5
CYP21A2 p.E238 Deletion as Result of Multiple Microconversion Events: A Genetic Study on an Italian Congenital Adrenal Hyperplasia (CAH) Family
20134 citationsauthor #3
Assessment of salivary free cortisol levels by liquid chromatography with tandem mass spectrometry (LC-MS/MS) in patients treated with mitotane
201218 citationsauthor #7
A vascular endothelial growth factor deficiency characterises scleroderma lung disease
201218 citationsauthor #10
Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient.
20125 citationsauthor #5
Polymorphisms in base excision DNA repair genes and association with melanoma risk in a pilot study on Central-South Italian population.
201213 citationsauthor #9
Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutations.
2012281 citationsauthor #4
allogeneic stem cell transplantation Role of fecal calprotectin as biomarker of gastrointestinal GVHD after
20120 citationsauthor #2
Rapid and simple identification of the commonest glucose-6-phosphate dehydrogenase (G6PD) Italian mutations: from DNA extraction to genotyping.
201211 citationsauthor #3
Reactive oxygen metabolites (ROMs) are associated with cardiovascular disease in chronic hemodialysis patients
20129 citationsauthor #5
Varespladib Inhibits Secretory Phospholipase A2 in Bronchoalveolar Lavage of Different Types of Neonatal Lung Injury
201229 citationsauthor #6
Re : Hypogonadotropic Hypogonadism in Morbidly Obese Males is Reversed After Bariatric Surgery
20120 citationsauthor #19
Combining Early Postoperative Parathyroid Hormone and Serum Calcium Levels Allows for an Efficacious Selective Post-thyroidectomy Supplementation Treatment
201258 citationsauthor #5
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients.
201214 citationsauthor #5
Role of fecal calprotectin as biomarker of gastrointestinal GVHD after allogeneic stem cell transplantation.
201222 citationsauthor #8
Circulating endothelial cells as marker of endothelial damage in male hypogonadism.
20125 citationsauthor #10
Blood presence of circulating oncofetal fibronectin mRNA, by RT-PCR, does not represent a useful specific marker for the management and follow-up of thyroid cancer patients
20123 citationsauthor #7
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis
20128 citationsauthor #3
Tuesday, 28 August 2012
20121 citationsauthor #3244
Retinal function and CFH-ARMS2 polymorphisms analysis: a pilot study in Italian AMD patients.
20127 citationsauthor #9
Measurement of 25-hydroxyvitamin vitamin D by liquid chromatography tandem-mass spectrometry with comparison to automated immunoassays
20127 citationsauthor #7
A Reversed-Phase HPLC Fluorimetric Method for Simultaneous Determination of Homocysteine- Related Thiols in Different Body Fluids
201121 citationsauthor #4
Multiplex ligation-dependent probe amplification analysis is useful for diagnosing congenital adrenal hyperplasia but requires a deep knowledge of CYP21A2 genetics.
201118 citationsauthor #4
Cardiovascular risk factors in healthy women with previous small for gestational age infants
20119 citationsauthor #4
With Suspected Acute Coronary Syndromes Pregnancy-Associated Plasma Protein A as Predictor of Outcome in Patients
20110 citationsauthor #3
Determination of asymmetric dimethyl arginine in human serum by liquid chromatography-tandem mass spectrometry: clinical application in hypertensive subjects
201110 citationsauthor #3
Common Genetic Variants of MUTYH are not Associated with Cutaneous Malignant Melanoma: Application of Molecular Screening by Means of High-Resolution Melting Technique in a Pilot Case-Control Study
20117 citationsauthor #7
Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation
20115 citationsauthor #7
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement.
20112 citationsauthor #7
High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism.
20112 citationsauthor #5
588 ANGIOTENSIN-CONVERTING ENZYME I/D POLYMORPHISM IS ASSOCIATED WITH SIGNIFICANTLY DIFFERENT VALUES OF HEPATIC VENOUS PRESSURE GRADIENT IN PATIENTS WITH LIVER CIRRHOSIS
20110 citationsauthor #4
Human growth hormone (GH) immunoassay: standardization and clinical implications
201113 citationsauthor #7
Angiotensin-Conversing Enzyme I/D Polymorphism is Associated With Significantly Different Values of Hepatic Venous Pressure Gradient in Patients With Liver Cirrhosis
20110 citationsauthor #6
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: comparison of two methods and implications in molecular diagnostics.
20112 citationsauthor #4
Role of distinct phospholipases A2 and their modulators in meconium aspiration syndrome in human neonates
201154 citationsauthor #6
Clinical accuracy of midnight salivary cortisol measured by automated electrochemiluminescence immunoassay method in Cushing's syndrome
201044 citationsauthor #9
Influence of blood sampling site on intact parathyroid hormone concentrations in hemodialysis patients.
201010 citationsauthor #4
ROLE of Fecal Calprotectin as BIOMARKER of Gvhd AFTER Allogeneic STEM CELL TRANSPLANTATION
20100 citationsauthor #6
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations
201049 citationsauthor #3
How the "A" to "C" conversion may create a new splice acceptor site?
20101 citationsauthor #2
Oxidative stress, nitric oxide, and diabetes.
2010353 citationsauthor #6
A simplified method for the determination of total homocysteine in plasma by electrospray tandem mass spectrometry.
201025 citationsauthor #4
G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population.
20108 citationsauthor #4
Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis.
201033 citationsauthor #4
A simple liquid chromatography-tandem mass spectrometry method for urinary free cortisol analysis: suitable for routine purpose
201023 citationsauthor #4
Glucose‐6‐phosphate dehydrogenase laboratory assay: How, when, and why?
2009143 citationsauthor #3
Effects of rehabilitation treatment on thyroid function
20096 citationsauthor #7
Bile acids cause secretory phospholipase A2 activity enhancement, revertible by exogenous surfactant administration
200946 citationsauthor #7
A new CYP21A2 nonsense mutation causing severe 21-hydroxylase deficiency
20097 citationsauthor #4
Anorexia and plasma levels of free tryptophan, branched chain amino acids, and ghrelin in hemodialysis patients.
200924 citationsauthor #6
Circulating bacterial-derived DNA fragments and markers of inflammation in chronic hemodialysis patients.
2009107 citationsauthor #4
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report.
200961 citationsauthor #5

TIMELINE

1980 1 citations

1983 1 citations

1984 3 citations

1985 0 citations

1986 32 citations

1987 9 citations

1989 8 citations

1991 38 citations

1993 38 citations

1994 24 citations

1995 11 citations

1996 159 citations

1997 2 citations

1998 0 citations

2000 28 citations

2001 44 citations

2002 97 citations

2003 131 citations

2004 637 citations

2005 98 citations

2006 449 citations

2007 333 citations

2008 242 citations

2009 562 citations

2010 546 citations

2011 143 citations

2012 509 citations

2013 246 citations

2014 141 citations

2015 86 citations

2016 109 citations

2017 151 citations

2018 5 citations

C. Zuppi

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