Giorgio Gimelli

7.7k citations
128 papers · 3.4k · h-index 27

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
  • Plant Science top 2%
    • Chromosomal and Genetic Variations

Papers in

  • Genetics 78
    • Genomic variations and chromosomal abnormalities 50
    • Genetics and Neurodevelopmental Disorders 20
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
  • Molecular Biology 59
    • Congenital heart defects research 14
Co-authors
Orsetta Zuffardi (29 shared papers)Cristina Cuoco (31 shared papers)Stefania Gimelli (26 shared papers)Roberto Giorda (13 shared papers)Sabrina Giglio (8 shared papers)Elisa Tassano (33 shared papers)Chris Tyler‐Smith (3 shared papers)William C. Earnshaw (3 shared papers)
Journals
Human Genetics (15 papers)European Journal of Medical Genetics (9 papers)Molecular Cytogenetics (8 papers)Cytogenetic and Genome Research (6 papers)Human Mutation (6 papers)
Partner nations
ItalyUnited StatesSwitzerland

In The Last Decade

Giorgio Gimelli

126 papers receiving 3.3k citations

Peers

Giorgio Gimelli
Comparison fields: 5 of 106
  • Genetics 1.9k
  • Plant Science 949
  • Molecular Biology 1.7k
  • Pediatrics, Perinatology and Child Health 495
  • Developmental Biology 36
Replace Cédric Le Caignec with:
Cédric Le Caignec France
Thomy de Ravel Belgium
Nicole de Leeuw Netherlands
Antonio Novelli Italy
Claudia Ruivenkamp Netherlands
Sylvie Langlois Canada
J P Fryns Belgium
Andreas Winterpacht Germany
Blake C. Ballif United States
Kwame Anyane‐Yeboa United States
Giorgio Gimelli relative to Cédric Le Caignec France Cédric Le Caignec's profile →
Citations per field
00.5×2×3.2×
Cédric Le Caignec · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 128 papers — load more, or switch the sort, to bring in the rest.

#Work
1
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
1997291
2
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
2001288
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
1989200
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
2002160
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
2001155
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
2007129
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
2007100
8
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
199998
9
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
199695
10
Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions
Human Molecular Genetics ·Giorgio Gimelli
200393
11
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
197977
12
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, Joanne Verheij, Roberto Giorda, Rita Grasso, Renato Borgatti, Filomena Pagone, Laura Rodríguez, Maria-Luisa Martinez-Frias, Conny van Ravenswaaij, Orsetta Zuffardi
200875
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
199367
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
200066
15
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
198661
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
199261
17
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
200061
18
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
200151
19
Duplication of the short arm of chromosome 9. Analysis of five cases
Human Genetics ·Cristina Cuoco, Giorgio Gimelli, Francesco Pasquali, L. Poloni, Orsetta Zuffardi, P. Alicata, G. Battaglino, Franck Bernardi, R. Cerone, M. Cotellessa, A. Ghidont, Santo Motta
198244
20
Microarray based analysis of an inherited terminal 3p26.3 deletion, containing only the CHL1 gene, from a normal father to his two affected children
Orphanet Journal of Rare Diseases ·Cristina Cuoco, Patrizia Ronchetto, Stefania Gimelli, Frédérique Béna, Maria Teresa Divizia, Margherita Lerone, Marisol Mirabelli-Badenier, M. Mascaretti, Giorgio Gimelli
201142

About Giorgio Gimelli

Giorgio Gimelli is a scholar working on Genetics, Molecular Biology, Surgery, Plant Science and Pulmonary and Respiratory Medicine, having authored 128 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (50 papers), Genetics and Neurodevelopmental Disorders (20 papers), Chromosomal and Genetic Variations (19 papers), Congenital heart defects research (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Prenatal Screening and Diagnostics (11 papers), Immunodeficiency and Autoimmune Disorders (8 papers) and Coronary Interventions and Diagnostics (8 papers). The work is most often cited by research in Genetics (1.9k citations), Plant Science (949 citations), Molecular Biology (1.7k citations), Pediatrics, Perinatology and Child Health (495 citations) and Developmental Biology (36 citations). Giorgio Gimelli has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Orsetta Zuffardi, Cristina Cuoco, Stefania Gimelli, Roberto Giorda, Sabrina Giglio, Elisa Tassano, Chris Tyler‐Smith, William C. Earnshaw, Peter E. Warburton and Margherita Lerone. Their work appears in journals such as Human Genetics, European Journal of Medical Genetics, Molecular Cytogenetics, Cytogenetic and Genome Research and Human Mutation.

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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