Massimo Attanasio

5.2k total citations
31 papers, 1.8k citations indexed

About

Massimo Attanasio is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Massimo Attanasio has authored 31 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 22 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Massimo Attanasio's work include Genetic and Kidney Cyst Diseases (21 papers), Renal and related cancers (17 papers) and Hedgehog Signaling Pathway Studies (6 papers). Massimo Attanasio is often cited by papers focused on Genetic and Kidney Cyst Diseases (21 papers), Renal and related cancers (17 papers) and Hedgehog Signaling Pathway Studies (6 papers). Massimo Attanasio collaborates with scholars based in United States, Germany and China. Massimo Attanasio's co-authors include Friedhelm Hildebrandt, Edgar A. Otto, John F. O’Toole, John A. Sayer, Matthias T. F. Wolf, Boris Utsch, Weibin Zhou, Corinne Antignac, Peter Nürnberg and Gudrun Nürnberg and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Scientific Reports.

In The Last Decade

Massimo Attanasio

31 papers receiving 1.7k citations

Peers

Countries citing papers authored by Massimo Attanasio

Since Specialization

Citations

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

Fields of papers citing papers by Massimo Attanasio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Massimo Attanasio

This figure shows the co-authorship network connecting the top 25 collaborators of Massimo Attanasio. A scholar is included among the top collaborators of Massimo Attanasio 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 Massimo Attanasio. Massimo Attanasio 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	Relative bioavailability of fedratinib through various alternative oral administration methods in healthy adults 2023 ·Cancer Chemotherapy and Pharmacology ·Yizhe Chen, D.J. Wyatt, Massimo Attanasio, Mark Thomas, Michael A. Thomas, Bing He, Rina Nishii, Liangang Liu, (unknown), Yongjun Xue, Leonidas N. Carayannopoulos, K. OGASAWARA, Gopal Krishna	2
2	A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome 2021 ·Clinical Genetics ·Nur Canpolat, (unknown), (unknown), Seha Saygılı, Nazlı Kara, Trudi A. Westfall, Qiong Ding, Bartley Brown, Terry A. Braun, Diane C. Slusarski, Kader Karlı Oğuz, Yasemin Özlük, Beyhan Tüysüz, Tuğba Öztürk, Lale Sever, Osman Uğur Sezerman, Rezan Topaloğlu, Salim Çalışkan, Massimo Attanasio, Fatih Özaltın	7
3	Loss of diacylglycerol kinase ε causes thrombotic microangiopathy by impairing endothelial VEGFA signaling 2021 ·JCI Insight ·(unknown), Qiong Ding, Dao‐Fu Dai, (unknown), Manasa K. Nayak, Can Li, (unknown), Heng Jin, Chang Shu, Anil K. Chauhan, Chou‐Long Huang, Massimo Attanasio	15
4	Detection of pro angiogenic and inflammatory biomarkers in patients with CKD 2021 ·Scientific Reports ·Diana Jalal, Bridget Sanford, Brandon Renner, Patrick Ten Eyck, Jennifer Laskowski, (unknown), (unknown), Yousef Zakharia, Douglas R. Spitz, Ayotunde O. Dokun, Massimo Attanasio, (unknown), Joshua M. Thurman	17
5	Epithelial innate immunity mediates tubular cell senescence after kidney injury 2019 ·JCI Insight ·Heng Jin, Yan Zhang, Qiong Ding, Shanshan Wang, Prerna Rastogi, Dao‐Fu Dai, Dongmei Lu, (unknown), Chao Cao, Angela Yee‐Moon Wang, (unknown), Chongyu Ren, (unknown), (unknown), Yanfen Chai, Diana Zepeda‐Orozco, Judith Campisi, Massimo Attanasio	98
6	Loss of Glis2/NPHP7 causes kidney epithelial cell senescence and suppresses cyst growth in the Kif3a mouse model of cystic kidney disease 2016 ·Kidney International ·Dongmei Lu, (unknown), Binghua Li, Chongyu Ren, Kayla McEnery, Jili Zhu, Moumita Chaki, Komal Vadnagara, (unknown), Anton M. Jetten, Peter Igarashi, Massimo Attanasio	33
7	Ciliopathies and DNA damage 2015 ·Current Opinion in Nephrology & Hypertension ·Massimo Attanasio	7
8	Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD 2014 ·Journal of the American Society of Nephrology ·Ekim Z. Taşkıran, Emine Korkmaz, Şafak Güçer, Can Koşukçu, Figen Kaymaz, (unknown), Elizabeth C. Bryda, Moumita Chaki, Dongmei Lu, Komal Vadnagara, Cengiz Candan, Rezan Topaloğlu, Franz Schaefer, Massimo Attanasio, Carsten Bergmann, Fatih Özaltın	31
9	Increased hedgehog signaling in postnatal kidney results in aberrant activation of nephron developmental programs 2011 ·Human Molecular Genetics ·Binghua Li, (unknown), (unknown), Ramanavelan Sakthivel, Peter Igarashi, Anton M. Jetten, Massimo Attanasio	33
10	The genetic components of idiopathic nephrolithiasis 2010 ·Pediatric Nephrology ·Massimo Attanasio	11
11	Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11) 2009 ·Journal of Medical Genetics ·Edgar A. Otto, Kálmán Tory, Massimo Attanasio, Weibin Zhou, Moumita Chaki, (unknown), Eric L. Wise, (unknown), Boris Utsch, C. Becker, Gudrun Nürnberg, Peter Nürnberg, Ahmet Nayır, Sophie Saunier, Corinne Antignac, Friedhelm Hildebrandt	98
12	Nephronophthisis 2009 ·Journal of the American Society of Nephrology ·Friedhelm Hildebrandt, Massimo Attanasio, Edgar A. Otto	249
13	Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing 2007 ·Human Mutation ·Edgar A. Otto, Juliana Helou, Susan J. Allen, John F. O’Toole, Eric L. Wise, Shazia Ashraf, Massimo Attanasio, Weibin Zhou, Matthias T. F. Wolf, Friedhelm Hildebrandt	60
14	Evidence of Oligogenic Inheritance in Nephronophthisis 2007 ·Journal of the American Society of Nephrology ·Julia Hoefele, Matthias T. F. Wolf, John F. O’Toole, Edgar A. Otto, Ulla T. Schultheiß, (unknown), Massimo Attanasio, Boris Utsch, Corinne Antignac, Friedhelm Hildebrandt	105
15	Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis 2007 ·Nature Genetics ·Massimo Attanasio, N. Henriette Uhlenhaut, Vitor H. Sousa, John F. O’Toole, Edgar A. Otto, Katrin Anlag, (unknown), (unknown), Juliana Helou, John A. Sayer, Dominik Seelow, Gudrun Nürnberg, Christian Becker, Albert E. Chudley, Peter Nürnberg, Friedhelm Hildebrandt, Mathias Treier	174
16	Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing 2006 ·Human Genetics ·Matthias T. F. Wolf, Bettina E. Mucha, Hans Christian Hennies, Massimo Attanasio, (unknown), Isabella Zalewski, Stephanie M. Karle, Edgar A. Otto, Constantinos Deltas, Arno Fuchshuber, Friedhelm Hildebrandt	16
17	Mutational analysis of theNPHP4 gene in 250 patients with nephronophthisis 2005 ·Human Mutation ·Julia Hoefele, Ralf Sudbrak, Richard Reinhardt, (unknown), Steffen Hennig, Anita Imm, (unknown), Boris Utsch, Massimo Attanasio, John F. O’Toole, Edgar A. Otto, Friedhelm Hildebrandt	46
18	Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome 2005 ·Pediatric Nephrology ·Boris Utsch, John A. Sayer, Massimo Attanasio, Rob Rodrigues Pereira, Michael R. Eccles, Hans-Christian Hennies, Edgar A. Otto, Friedhelm Hildebrandt	65
19	Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2–q34.2 by total genome search for linkage 2005 ·Nephrology Dialysis Transplantation ·Matthias T. F. Wolf, Isabella Zalewski, Félix Claverie-Martı́n, Rainer Ruf, Dominik N. Müller, Hans Christian Hennies, (unknown), (unknown), Massimo Attanasio, (unknown), Anita Imm, Barbara Lucke, Boris Utsch, Edgar A. Otto, Peter Nürnberg, Víctor Manuel García Nieto, Friedhelm Hildebrandt	20
20	Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains 2003 ·Kidney International ·Matthias T. F. Wolf, Bettina E. Mucha, Massimo Attanasio, Isabella Zalewski, Stephanie M. Karle, Hartmut P.H. Neumann, Nazneen Rahman, (unknown), C. A. Baldamus, Edgar A. Otto, Ralph Witzgall, Arno Fuchshuber, Friedhelm Hildebrandt	69

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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