G Pescia

1.5k total citations
65 papers, 1.1k citations indexed

About

G Pescia is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, G Pescia has authored 65 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 22 papers in Pediatrics, Perinatology and Child Health and 18 papers in Molecular Biology. Recurrent topics in G Pescia's work include Prenatal Screening and Diagnostics (14 papers), Ocular Oncology and Treatments (11 papers) and Genomic variations and chromosomal abnormalities (9 papers). G Pescia is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Ocular Oncology and Treatments (11 papers) and Genomic variations and chromosomal abnormalities (9 papers). G Pescia collaborates with scholars based in Switzerland, France and United States. G Pescia's co-authors include Daniel F. Schorderet, Léonidas Zografos, Elena Korvatska, Denis Le Paslier, K. Evans, Ioannis Xénarios, Christian Iseli, Bernard Conrad, Nicolas Guex and Francis L. Munier and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and The Journal of Pediatrics.

In The Last Decade

G Pescia

58 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
G Pescia Switzerland 15 409 316 313 310 170 65 1.1k
Juan Chemke Israel 20 365 0.9× 220 0.7× 45 0.1× 327 1.1× 25 0.1× 64 1.1k
Pedro F. Lopez United States 25 872 2.1× 92 0.3× 1.4k 4.4× 74 0.2× 2.1k 12.2× 53 2.6k
Inge B. Mathijssen Netherlands 17 379 0.9× 173 0.5× 26 0.1× 192 0.6× 31 0.2× 30 740
S. Pezzotta Italy 16 144 0.4× 77 0.2× 121 0.4× 67 0.2× 64 0.4× 44 708
George E. Sanborn United States 21 276 0.7× 36 0.1× 606 1.9× 101 0.3× 1.4k 8.4× 56 1.8k
Ruth van der Gaag Netherlands 15 83 0.2× 60 0.2× 219 0.7× 42 0.1× 216 1.3× 26 780
Hana Abouzeid Switzerland 18 226 0.6× 57 0.2× 259 0.8× 184 0.6× 397 2.3× 46 785
Niema Ibrahim Saudi Arabia 17 411 1.0× 77 0.2× 13 0.0× 257 0.8× 46 0.3× 22 767
Hadia Hijazi Saudi Arabia 11 333 0.8× 84 0.3× 59 0.2× 226 0.7× 77 0.5× 15 579
A H Chignell United Kingdom 20 265 0.6× 25 0.1× 1.1k 3.5× 57 0.2× 1.4k 8.4× 70 1.7k

Countries citing papers authored by G Pescia

Since Specialization
Citations

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

Fields of papers citing papers by G Pescia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G Pescia

This figure shows the co-authorship network connecting the top 25 collaborators of G Pescia. A scholar is included among the top collaborators of G Pescia 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 G Pescia. G Pescia is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Pescia, G, Nicolas Guex, Christian Iseli, et al.. (2016). Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases. Genetics in Medicine. 19(2). 169–175. 73 indexed citations
2.
Ramelli, Gian Paolo, et al.. (2008). Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study. Developmental Medicine & Child Neurology. 50(12). 953–955. 23 indexed citations
3.
Wunder, Dorothea, et al.. (2004). Maternal serum levels of placental proteins after in vitro fertilisation and their implications for prenatal screening. Prenatal Diagnosis. 24(6). 471–477. 28 indexed citations
4.
Schorderet, Daniel F., et al.. (2001). Further delineation of the facial 13q14 deletion syndrome in 13 retinoblastoma patients. Ophthalmic Genetics. 22(1). 11–18. 16 indexed citations
5.
Pescia, G. (1997). Genetic services in Switzerland.. PubMed. 5 Suppl 2. 174–7. 1 indexed citations
6.
7.
8.
Krupp, Serge, et al.. (1994). Mid-term results with cultured epidermal autografts, allogenic skin transplants and cyclosporin A medication. Burns. 20(1). 15–20. 5 indexed citations
9.
Munier, Francis L., A. Linn Murphree, Pamela Flodman, et al.. (1994). Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees. Human Genetics. 94(5). 484–90. 11 indexed citations
10.
Ciafaloni, Emma, Filippo M. Santorelli, Sara Shanske, et al.. (1993). Maternally inherited Leigh syndrome. The Journal of Pediatrics. 122(3). 419–422. 74 indexed citations
11.
Grandi, P. De, et al.. (1992). [Ultrasonic diagnosis of a hereditary multiple malformation syndrome: Meckel-Gruber syndrome or Carpenter-Hunter syndrome].. PubMed. 21(8). 928–33. 2 indexed citations
12.
Munier, Francis L., Aubin Balmer, Carl Moos, et al.. (1991). Consultation Lausannoise du Rétinoblastome, 1986-1990: Délétions au locus de l'estérase D dans un collectif de 128 patients*. Klinische Monatsblätter für Augenheilkunde. 198(5). 419–424. 2 indexed citations
13.
Paccaud, Fred, et al.. (1988). [Strategies in screening for chromosome number aberrations in women younger than 35 years of age].. PubMed. 45(10). 682–7.
14.
Munier, Francis L., et al.. (1988). A ?new? allele of esterase D in a retinoblastoma family. Human Genetics. 78(3). 289–290. 5 indexed citations
15.
Munier, Francis L., et al.. (1987). [Historical notes on retinoblastoma: apropos of 2 ancient terracotta figures].. PubMed. 107(7). 591–7. 2 indexed citations
16.
Evans, K., et al.. (1979). A family study of renal agenesis. Journal of Medical Genetics. 16(3). 176–188. 70 indexed citations
17.
Pescia, G, et al.. (1979). Fausses-couches précoces itératives et caryotype. Etude cytogénétique de 80 couples consécutifs.. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 8(1). 3 indexed citations
18.
Pescia, G, et al.. (1979). [Distal 9q trisomy phenotype in a patient with a supernumerary rearranged chromosome [t(X:9)] (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 158–62. 5 indexed citations
19.
Pescia, G, et al.. (1978). [Peutz-Jeghers' syndrome, intussusception and associated malignancies (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 104(2). 117–30. 7 indexed citations
20.
Pescia, G, et al.. (1977). [Three families with pericentric inversion of chromosome 9].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 25(2). 121–34. 4 indexed citations

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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