Michela Barbaro

2.2k total citations
47 papers, 1.3k citations indexed

About

Michela Barbaro is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Michela Barbaro has authored 47 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 25 papers in Genetics and 14 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Michela Barbaro's work include Sexual Differentiation and Disorders (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers) and Metabolism and Genetic Disorders (9 papers). Michela Barbaro is often cited by papers focused on Sexual Differentiation and Disorders (21 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (17 papers) and Metabolism and Genetic Disorders (9 papers). Michela Barbaro collaborates with scholars based in Sweden, Italy and Germany. Michela Barbaro's co-authors include Anna Wedell, Svetlana Lajić, Antonio Balsamo, Mikael Oscarson, Johan Staaf, K Naess, Rolf Wibom, Rolf Zetterström, Lilia Baldazzi and Anna Wedell and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and Human Reproduction.

In The Last Decade

Michela Barbaro

45 papers receiving 1.3k citations

Peers

Countries citing papers authored by Michela Barbaro

Since Specialization

Citations

This map shows the geographic impact of Michela Barbaro'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 Michela Barbaro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michela Barbaro more than expected).

Fields of papers citing papers by Michela Barbaro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michela Barbaro. 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 Michela Barbaro. The network helps show where Michela Barbaro may publish in the future.

Co-authorship network of co-authors of Michela Barbaro

This figure shows the co-authorship network connecting the top 25 collaborators of Michela Barbaro. A scholar is included among the top collaborators of Michela Barbaro 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 Michela Barbaro. Michela Barbaro 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	PARKIN is not required to sustain OXPHOS function in adult mammalian tissues 2024 ·npj Parkinson s Disease ·Roberta Filograna, (unknown), (unknown), Giovanni Rigoni, Michela Barbaro, Mikael Oscarson, Seungmin Lee, Katarína Tiklová, Markus Ringnér, Camilla Koolmeister, Rolf Wibom, Sara Riggare, Inger Nennesmo, Thomas Perlmann, Anna Wredenberg, Anna Wedell, Elisa Motori, Per Svenningsson, Nils‐Göran Larsson	10
2	First Year of TREC-Based National SCID Screening in Sweden 2021 ·International Journal of Neonatal Screening ·(unknown), Olov Ekwall, Mikael Sundin, Nicholas Brodszki, Anders Fasth, Per Marits, (unknown), Susanne Jönsson, Michela Barbaro, Anna Wedell, Ulrika von Döbeln, Rolf Zetterström	17
3	Novel non-classic CYP21A2 variants, including combined alleles, identified in patients with congenital adrenal hyperplasia 2019 ·Clinical Biochemistry ·Leif Karlsson, (unknown), (unknown), (unknown), (unknown), Bengt Persson, Gil Guerra‐Júnior, Sofia Helena Valente de Lemos‐Marini, Lilia Baldazzi, Soara Menabò, Antonio Balsamo, Nella Augusta Greggio, Maricilda Palandi de Mello, Michela Barbaro, Svetlana Lajić	2
4	Newborn Screening for Primary Immune Deficiencies with a TREC/KREC/ACTB Triplex Assay—A Three-Year Pilot Study in Sweden 2017 ·International Journal of Neonatal Screening ·Rolf Zetterström, Michela Barbaro, Annika Ohlsson, Stephan Borte, Susanne Jönsson, Jacek Winiarski, Ulrika von Döbeln, Lennart Hammarström	14
5	Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden—a 2-Year Pilot TREC and KREC Screening Study 2016 ·Journal of Clinical Immunology ·Michela Barbaro, Annika Ohlsson, Stephan Borte, Susanne Jönsson, Rolf Zetterström, Jovanka King, Jacek Winiarski, Ulrika von Döbeln, Lennart Hammarström	100
6	Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform 2014 ·Human Reproduction ·(unknown), Angelica Lindén Hirschberg, Kenny A. Rodriguez‐Wallberg, Erik Iwarsson, Anna Wedell, Michela Barbaro	43
7	Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism 2014 ·BMC Genomics ·Henrik Stranneheim, Martin Engvall, K Naess, Nicole Lesko, Pontus Larsson, (unknown), (unknown), Anna Wredenberg, Christoph Freyer, Michela Barbaro, Helene Bruhn, (unknown), Måns Magnusson, Rolf Wibom, Rolf Zetterström, Valtteri Wirta, Ulrika von Döbeln, Anna Wedell	44
8	Novel candidate genes for 46,XY gonadal dysgenesis identified by a customized 1 M array-CGH platform 2013 ·European Journal of Medical Genetics ·(unknown), Angelica Lindén Hirschberg, Erik Iwarsson, Bengt Persson, Anna Wedell, Michela Barbaro	15
9	Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion 2012 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Yohann Grondin, (unknown), Luis E. Figuera, Rocío Ortiz‐López, Michela Barbaro	5
10	Partial Deletion of the <i>NR5A1 (SF1)</i> Gene Detected by Synthetic Probe MLPA in a Patient with XY Gonadal Disorder of Sex Development 2011 ·Sexual Development ·Michela Barbaro, Martine Cools, Leendert H. J. Looijenga, S L S Drop, Anna Wedell	25
11	Disorders of sex development 2011 ·Seminars in Fetal and Neonatal Medicine ·Michela Barbaro, Anna Wedell, Anna Nordenström	20
12	Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome 2011 ·JIMD Reports ·K Naess, Michela Barbaro, Helene Bruhn, Rolf Wibom, Inger Nennesmo, Ulrika von Döbeln, Nils‐Göran Larsson, Antal Németh, Nicole Lesko	4
13	Gene dosage imbalances in patients with 46,XY gonadal DSD detected by an in‐house‐designed synthetic probe set for multiplex ligation‐dependent probe amplification analysis 2008 ·Clinical Genetics ·Michela Barbaro, Alessandro Cicognani, Antonio Balsamo, A. Löfgren, Lilia Baldazzi, Anna Wedell, Mikael Oscarson	33
14	Array-CGH identifies cyclin D1 and UBCH10 amplicons in anaplastic thyroid carcinoma 2008 ·Endocrine Related Cancer ·J. Jack Lee, Amy Au, Theodoros Foukakis, Michela Barbaro, Nicole Kiss, Roderick Clifton‐Bligh, Johan Staaf, (unknown), Leigh Delbridge, Bruce G. Robinson, Göran Wallin, (unknown), Catharina Larsson	43
15	Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms 2008 ·European Journal of Human Genetics ·(unknown), Claudia Ruivenkamp, Johan Staaf, Hongbo Zhu, Michela Barbaro, David Petillo, Sok Kean Khoo, Åke Borg, Yao‐Shan Fan, Jacqueline Schoumans	26
16	Complete androgen insensitivity without Wolffian duct development: the AR‐A form of the androgen receptor is not sufficient for male genital development 2007 ·Clinical Endocrinology ·Michela Barbaro, Mikael Oscarson, (unknown), Hans Hamberg, Anna Wedell	5
17	Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia 2006 ·Journal of Molecular Medicine ·(unknown), Christine Bellanné‐Chantelot, Michela Barbaro, Sylvie Cabrol, Anna Wedell, Svetlana Lajić	25
18	Functional studies of two novel and two rare mutations in the 21-hydroxylase gene 2006 ·Journal of Molecular Medicine ·Michela Barbaro, Lilia Baldazzi, Antonio Balsamo, Svetlana Lajić, (unknown), (unknown), Piero Pirazzoli, E Cacciari, Alessandro Cicognani, Anna Wedell	26
19	Not All Amino Acid Substitutions of the Common Cluster E6 Mutation inCYP21Cause Congenital Adrenal Hyperplasia 2005 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), Michela Barbaro, Svetlana Lajić, Anna Wedell	19
20	Functional Analysis of Two Recurrent Amino Acid Substitutions in theCYP21Gene from Italian Patients with Congenital Adrenal Hyperplasia 2004 ·The Journal of Clinical Endocrinology & Metabolism ·Michela Barbaro, Svetlana Lajić, Lilia Baldazzi, Antonio Balsamo, Piero Pirazzoli, Alessandro Cicognani, Anna Wedell, E Cacciari	42

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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