Giorgio Gimelli

7.8k citations

130 papers · 3.7k · h-index 30

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics

Papers in

Genetics 73
- Genomic variations and chromosomal abnormalities 45
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
- Genetics and Neurodevelopmental Disorders 14
Molecular Biology 54
- Congenital heart defects research 14

Co-authors: Orsetta Zuffardi (29 shared papers)Cristina Cuoco (33 shared papers)Roberto Giorda (13 shared papers)Stefania Gimelli (26 shared papers)Sabrina Giglio (8 shared papers)Elisa Tassano (33 shared papers)M. Fraccaro (8 shared papers)William C. Earnshaw (3 shared papers)
Journals: Human Genetics (15 papers)European Journal of Medical Genetics (9 papers)Molecular Cytogenetics (8 papers)Human Mutation (6 papers)Seminars in Dialysis (5 papers)
Partner nations: Italy United States Switzerland

In The Last Decade

Giorgio Gimelli

127 papers receiving 3.5k citations

Peers

Countries citing papers authored by Giorgio Gimelli

Since Specialization

Citations

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

Fields of papers citing papers by Giorgio Gimelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Giorgio Gimelli, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Giorgio Gimelli Line = papers co-authored together Giorgio Gimelli links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 130 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements The American Journal of Human Genetics ·Sabrina Giglio, Karl W. Broman, Naomichi Matsumoto, Vladimiro Calvari, Giorgio Gimelli, Thomas Neumann, Hirofumi Ohashi, Lucille Voullaire, Daniela Larizza, Roberto Giorda, Jim L. Weber, David H. Ledbetter, Orsetta Zuffardi	2001	302
2	Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres Current Biology ·Peter E. Warburton, Carol Cooke, Sylvie Bourassa, Omid Vafa, Beth A. Sullivan, Gail Stetten, Giorgio Gimelli, Dorothy Warburton, Chris Tyler‐Smith, Kevin F. Sullivan, Guy G. Poirier, William C. Earnshaw	1997	298
3	Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. Proceedings of the National Academy of Sciences ·Andrea Ballabio, Barbara Bardoni, Rosalba Carrozzo, Generoso Andria, David Bick, L. B. Campbell, Ben C.J. Hamel, M.A. Ferguson‐Smith, Giorgio Gimelli, M. Fraccaro	1989	218
4	Heterozygous Submicroscopic Inversions Involving Olfactory Receptor–Gene Clusters Mediate the Recurrent t(4;8)(p16;p23) Translocation The American Journal of Human Genetics ·Sabrina Giglio, Vladimiro Calvari, Giuliana Gregato, Giorgio Gimelli, Silvia Camanini, Roberto Giorda, Angela Ragusa, Silvana Guerneri, Angelo Selicorni, Marcus Stumm, Holger Tönnies, Mario Ventura, Marcella Zollino, Giovanni Neri, John Barber, Dagmar Wieczorek, Mariano Rocchi, Orsetta Zuffardi	2002	187
5	Intravascular ultrasound criteria for the assessment of the functional significance of intermediate coronary artery stenoses and comparison with fractional flow reserve The American Journal of Cardiology ·Carlo Briguori, Angelo Anzuini, Flavio Airoldi, Giorgio Gimelli, Takahiro Nishida, Milena Adamian, Nicola Corvaja, Carlo Di Mario, Antonio Colombo	2001	160
6	Characterization of a recurrent 15q24 microdeletion syndrome Human Molecular Genetics ·Andrew J. Sharp, Rebecca R. Selzer, Joris A. Veltman, Stefania Gimelli, Giorgio Gimelli, Pasquale Striano, Antonietta Coppola, Regina Regan, Sue Price, Nine V.A.M. Knoers, Peggy S. Eis, Han G. Brunner, Raoul C. M. Hennekam, Samantha J.L. Knight, Bert B.A. de Vries, Orsetta Zuffardi, Evan E. Eichler	2007	135
7	Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation Human Mutation ·Renata Bocciardi, Roberto Giorda, Jens Buttgereit, Stefania Gimelli, Maria Teresa Divizia, Silvana Beri, Silvio Garofalo, Sara Tavella, Margherita Lerone, Orsetta Zuffardi, Michael Bäder, Roberto Ravazzolo, Giorgio Gimelli	2007	108
8	Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions Human Molecular Genetics ·Giorgio Gimelli	2003	102
9	Transmission of a Fully Functional Human Neocentromere through Three Generations The American Journal of Human Genetics ·Chris Tyler‐Smith, Giorgio Gimelli, Sabrina Giglio, Giovanna Floridia, Arpita Pandya, G. L. Terzoli, Peter E. Warburton, William C. Earnshaw, Orsetta Zuffardi	1999	101
10	The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. PubMed ·Giovanna Floridia, M. Piantanida, Antonella Minelli, Claudia Dellavecchia, María Clara Bonaglia, Elena Rossi, Giorgio Gimelli, Gianfranco Croci, Fabrizia Franchi, S Gilgenkrantz, Paola Grammatico, Leda Dalprà, Stephen Wood, Cesare Danesino, Orsetta Zuffardi	1996	98
11	Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype European Journal of Human Genetics ·María Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, Stefania Gimelli, Susan Marelli, (unknown), Roberto Giorda, Rita Grasso, Renato Borgatti, Filomena Pagone, Laura Rodríguez, Maria-Luisa Martinez-Frias, Conny van Ravenswaaij, Orsetta Zuffardi	2008	96
12	Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency Human Genetics ·L. Tiepolo, P Maraschio, Giorgio Gimelli, Cristina Cuoco, G Gargani, Claudio Romano	1979	90
13	Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability Human Genetics ·Annalisa Pezzolo, Giorgio Gimelli, Amnon Cohen, Antonella Lavaggetto, Cesare P.R. Romano, Giuseppina Fogu, Orsetta Zuffardi	1993	73
14	Genetic variation in ICF syndrome: Evidence for genetic heterogeneity Human Mutation ·Cisca Wijmenga, R. Scott Hansen, Giorgio Gimelli, Erik J. Bj�rck, E. Graham Davies, David L. Valentine, Bernd H. Belohradsky, Jacques J. M. van Dongen, Dominique Smeets, Lambert P.W.J. van den Heuvel, Jan A.F.M. Luyten, Eric Strengman, Corry M.R. Weemaes, P. Pearson	2000	71
15	Deletion of a 5-cM Region at Chromosome 8p23 Is Associated With a Spectrum of Congenital Heart Defects Circulation ·Sabrina Giglio, Sharon Graw, Giorgio Gimelli, Barbara Pirola, Paolo Varone, Lucille Voullaire, Franco Lerzo, Elena Rossi, Claudia Dellavecchia, María Clara Bonaglia, M. Cristina Digilio, Aldo Giannotti, Bruno Marino, Romeo Carrozzo, Julie R. Korenberg, Cesare Danesino, Eva Sujansky, Bruno Dallapiccola, Orsetta Zuffardi	2000	70
16	Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10 Pediatric Surgery International ·Giuseppe Martucciello, Maria Patrizia Bicocchi, P Dodero, Margherita Lerone, Michele Cirillo, Aldamaria Puliti, Giorgio Gimelli, Giovanni Romeo, Vincenzo Jasonni	1992	70
17	First trimester fetal karyotyping: one thousand diagnoses Human Genetics ·Giuseppe Simoni, Giorgio Gimelli, Cristina Cuoco, Lorenza Romitti, G. L. Terzoli, Silvana Guerneri, Franca Rossella, L. Pescetto, Annalisa Pezzolo, Simona Porta, B. Brambati, E. Porro, M. Fraccaro	1986	67
18	Discordance Between Prenatal Cytogenetic Diagnosis after Chorionic Villi Sampling and Chromosomal Constitution of the Fetus Giuseppe Simoni, Giorgio Gimelli, Cristina Cuoco, G. L. Terzoli, F. Rossella, Lorenza Romitti, Leda Dalprà, G. Nocera, M.G. Tibiletti, P. Tenti, M. Fraccaro	1985	56
19	Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication Human Genetics ·Anwarul K. Hassan, Thomas H. Norwood, Giorgio Gimelli, Stanley M. Gartler, Scott R. Hansen	2001	52
20	Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract Human Mutation ·Stefania Gimelli, Gianluca Caridi, Silvana Beri, Kyle W. McCracken, Renata Bocciardi, Paola Zordan, Monica Dagnino, Patrizia Fiorio, Luisa Murer, Elisa Benetti, Orsetta Zuffardi, Roberto Giorda, James M. Wells, Giorgio Gimelli, Gian Marco Ghiggeri	2010	46

About Giorgio Gimelli

Giorgio Gimelli is a scholar working on Genetics, Molecular Biology, Surgery, Plant Science and Pulmonary and Respiratory Medicine, having authored 130 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (45 papers), Chromosomal and Genetic Variations (17 papers), Congenital heart defects research (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (14 papers), Prenatal Screening and Diagnostics (12 papers), Immunodeficiency and Autoimmune Disorders (8 papers) and Coronary Interventions and Diagnostics (7 papers). The work is most often cited by research in Genetics (1.9k citations), Pediatrics, Perinatology and Child Health (522 citations), Molecular Biology (1.7k citations), Plant Science (928 citations) and Developmental Biology (30 citations). Giorgio Gimelli has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Orsetta Zuffardi, Cristina Cuoco, Roberto Giorda, Stefania Gimelli, Sabrina Giglio, Elisa Tassano, M. Fraccaro, William C. Earnshaw, Chris Tyler‐Smith and Peter E. Warburton. Their work appears in journals such as Human Genetics, European Journal of Medical Genetics, Molecular Cytogenetics, Human Mutation and Seminars in Dialysis.

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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