Nadia Soriani

628 total citations
22 papers, 446 citations indexed

About

Nadia Soriani is a scholar working on Molecular Biology, Hematology and Nutrition and Dietetics. According to data from OpenAlex, Nadia Soriani has authored 22 papers receiving a total of 446 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Hematology and 5 papers in Nutrition and Dietetics. Recurrent topics in Nadia Soriani's work include Iron Metabolism and Disorders (7 papers), Trace Elements in Health (5 papers) and Cancer Genomics and Diagnostics (4 papers). Nadia Soriani is often cited by papers focused on Iron Metabolism and Disorders (7 papers), Trace Elements in Health (5 papers) and Cancer Genomics and Diagnostics (4 papers). Nadia Soriani collaborates with scholars based in Italy, United States and Spain. Nadia Soriani's co-authors include Maurizio Ferrari, Laura Cremonesi, Silvia Galbiati, Paolo Arosio, Rita Paroni, Sonia Levi, Francesco Damin, Marcella Chiari, Isabella Fermo and Mario Cazzola and has published in prestigious journals such as Blood, PLoS ONE and Journal of Hepatology.

In The Last Decade

Nadia Soriani

21 papers receiving 440 citations

Peers

Countries citing papers authored by Nadia Soriani

Since Specialization

Citations

This map shows the geographic impact of Nadia Soriani's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Nadia Soriani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nadia Soriani more than expected).

Fields of papers citing papers by Nadia Soriani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nadia Soriani. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Nadia Soriani. The network helps show where Nadia Soriani may publish in the future.

Co-authorship network of co-authors of Nadia Soriani

This figure shows the co-authorship network connecting the top 25 collaborators of Nadia Soriani. A scholar is included among the top collaborators of Nadia Soriani based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nadia Soriani. Nadia Soriani is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Early increase in circulating carbonic anhydrase IX: A potential new predictive biomarker of preeclampsia 2023 ·Frontiers in Molecular Biosciences ·Silvia Galbiati, (unknown), Alessandro Ambrosi, Nadia Soriani, (unknown), Massimo Locatelli, Roberta Lucianò, Massimo Candiani, Luca Valsecchi, Gianpaolo Zerbini, Maddalena Smid	4
2	Small EVs-Associated DNA as Complementary Biomarker to Circulating Tumor DNA in Plasma of Metastatic Colorectal Cancer Patients 2021 ·Pharmaceuticals ·Silvia Galbiati, Francesco Damin, (unknown), (unknown), Nadia Soriani, Anna Maria Ferretti, Valentina Burgio, Monica Ronzoni, Riccardo Vago, Laura Solá, Marcella Chiari	15
3	Microarray Approach Combined with ddPCR: An Useful Pipeline for the Detection and Quantification of Circulating Tumour DNA Mutations 2019 ·Cells ·Silvia Galbiati, Francesco Damin, (unknown), Nadia Soriani, Valentina Burgio, Monica Ronzoni, Luca Gianni, Maurizio Ferrari, Marcella Chiari	12
4	Evaluation of three advanced methodologies, COLD-PCR, microarray and ddPCR, for identifying the mutational status by liquid biopsies in metastatic colorectal cancer patients 2018 ·Clinica Chimica Acta ·Silvia Galbiati, Francesco Damin, Valentina Burgio, Angela Brisci, Nadia Soriani, (unknown), Chiara Di Resta, Luca Gianni, Marcella Chiari, Monica Ronzoni, Maurizio Ferrari	20
5	Analysis of KRAS, NRAS and BRAF mutational profile by combination of in-tube hybridization and universal tag-microarray in tumor tissue and plasma of colorectal cancer patients 2018 ·PLoS ONE ·Francesco Damin, Silvia Galbiati, Nadia Soriani, Valentina Burgio, Monica Ronzoni, Maurizio Ferrari, Marcella Chiari	17
6	COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma 2016 ·Journal of Medical Genetics ·Silvia Galbiati, (unknown), Francesco Damin, Nadia Soriani, (unknown), Carlo Castellani, Federica Natacci, Cristina Curcio, Manuela Seia, Faustina Lalatta, Marcella Chiari, Maurizio Ferrari, Laura Cremonesi	27
7	Urinary Citrate in Recurrent Stone-Forming Patients 2015 ·Contributions to nephrology ·A. Aroldi, Nadia Soriani, Roberto Zubani, Claudia Castelnovo, G. Graziani	0
8	High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene 2010 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·(unknown), Nadia Soriani, Domenico Girelli, Clara Camaschella, Ivana Spiga, Matteo Giovanni Della Porta, Maurizio Ferrari, Laura Cremonesi	6
9	Clinical, pathological, and molecular correlates in ferroportin disease: A study of two novel mutations 2008 ·Journal of Hepatology ·Domenico Girelli, Ivana De Domenico, Claudia Bozzini, Natascia Campostrini, Fabiana Busti, Annalisa Castagna, Nadia Soriani, Laura Cremonesi, Maurizio Ferrari, Romano Colombari, Diane M. Ward, Jerry Kaplan, Roberto Corrocher	34
10	Molecular Scanning of the ABCA4 Gene in Spanish Patients with Retinitis Pigmentosa and Stargardt Disease: Identification of Novel Mutations 2007 ·European Journal of Ophthalmology ·Stefania Stenirri, (unknown), Nadia Soriani, Sara Bernal, Montserrat Baiget, Maurizio Ferrari, Laura Cremonesi	2
11	Clinical, Pathological, and Molecular Correlates in Ferroportin Disease. A Study of Two Novel Mutations. 2007 ·Blood ·Domenico Girelli, Ivana De Domenico, Claudia Bozzini, Ilaria Tenuti, Nadia Soriani, Fabiana Busti, Laura Cremonesi, Jerry Kaplan, Roberto Corrocher	2
12	Genetic and clinical heterogeneity of ferroportin disease 2005 ·British Journal of Haematology ·(unknown), (unknown), Nadia Soriani, (unknown), Isabella Fermo, Filomena Daraio, Anna Gallì, Daniela Pietra, Luca Malcovati, Maurizio Ferrari, Clara Camaschella, M. Cazzola	49
13	Denaturing HPLC Profiling of the ABCA4 Gene for Reliable Detection of Allelic Variations 2004 ·Clinical Chemistry ·Stefania Stenirri, Isabella Fermo, (unknown), Silvia Galbiati, Nadia Soriani, Rita Paroni, Maria Pia Manitto, (unknown), R. Brancato, Rando Allikmets, Maurizio Ferrari, Laura Cremonesi	32
14	Scanning mutations of the 5′UTR regulatory sequence of l‐ferritin by denaturing high‐performance liquid chromatography: identification of new mutations 2003 ·British Journal of Haematology ·Laura Cremonesi, Rita Paroni, Barbara Foglieni, Silvia Galbiati, Isabella Fermo, Nadia Soriani, (unknown), Giuseppina Ruggeri, Giorgio Biasiotto, Mario Cazzola, Francesca Ferrari, Maurizio Ferrari, Paolo Arosio	27
15	Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3) 2002 ·British Journal of Haematology ·Mario Cazzola, Laura Cremonesi, Maria Papaioannou, Nadia Soriani, Anna Kioumi, (unknown), Rita Paroni, (unknown), Sonia Levi, Maurizio Ferrari, Paolo Arosio, John Christakis	72
16	Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients 2001 ·Human Genetics ·(unknown), Maurizio Ferrari, Nadia Soriani, A. Gessi, Barbara Foglieni, (unknown), Maria Pia Manitto, R. Brancato, Michael Dean, Rando Allikmets, Laura Cremonesi	41
17	Double-Gradient Denaturing Gradient Gel Electrophoresis Assay for Identification of L-Ferritin Iron-responsive Element Mutations Responsible for Hereditary Hyperferritinemia-Cataract Syndrome: Identification of the New Mutation C14G 2001 ·Clinical Chemistry ·Laura Cremonesi, (unknown), Nadia Soriani, Maurizio Ferrari, Sonia Levi, (unknown), Giuseppina Ruggeri, Paolo Arosio	31
18	Seven Novel Additional Small Mutations and a New Alternative Splicing in the Human Dystrophin Gene Detected by Heteroduplex Analysis and Restricted RT-PCR Heteroduplex Analysis of Illegitimate Transcripts 1996 ·European Journal of Human Genetics ·Annalisa Barbieri, Nadia Soriani, Alessandra Ferlini, (unknown), Maurizio Ferrari, Paola Carrera	27
19	A nonsense mutation (Gln-673-Term) in exon 17 of the human dystrophin gene detected by heteroduplex analysis 1995 ·Human Genetics ·(unknown), Nadia Soriani, (unknown), Maurizio Ferrari, Paola Carrera	1
20	Mutational analysis of muscle and brain specific promoter regions of dystrophin gene in DMD/BMD Italian patients by denaturing gradient gel electrophoresis (DGGE) 1995 ·Molecular and Cellular Probes ·(unknown), Paola Carrera, Nadia Soriani, Lucía Morandi, Maurizio Ferrari	5

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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