Chiara Palka

734 total citations
34 papers, 468 citations indexed

About

Chiara Palka is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Chiara Palka has authored 34 papers receiving a total of 468 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 10 papers in Molecular Biology. Recurrent topics in Chiara Palka's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (12 papers) and Fetal and Pediatric Neurological Disorders (7 papers). Chiara Palka is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (12 papers) and Fetal and Pediatric Neurological Disorders (7 papers). Chiara Palka collaborates with scholars based in Italy, United States and Israel. Chiara Palka's co-authors include Liborio Stuppia, Paolo Guanciali‐Franchi, Giuseppe Calabrese, Valentina Gatta, Gian Mario Tiboni, Elisena Morizio, Antonino Uncini, Maria Vittoria De Angelis, Antonio Di Muzio and Oronzo Scarciolla and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Gene.

In The Last Decade

Chiara Palka

29 papers receiving 441 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chiara Palka Italy	10	255	210	136	95	50	34	468
Suzanne Braga Switzerland	9	203 0.8×	124 0.6×	92 0.7×	60 0.6×	54 1.1×	15	387
Alida C. Knegt Netherlands	14	271 1.1×	257 1.2×	232 1.7×	16 0.2×	74 1.5×	35	652
Alison Lashwood United Kingdom	10	141 0.6×	168 0.8×	268 2.0×	34 0.4×	25 0.5×	20	439
Azzedine Aboura France	17	311 1.2×	525 2.5×	258 1.9×	53 0.6×	61 1.2×	40	767
Andrea Kwan United States	14	209 0.8×	260 1.2×	55 0.4×	27 0.3×	32 0.6×	19	553
Georgia Kakourou Greece	12	163 0.6×	144 0.7×	361 2.7×	70 0.7×	118 2.4×	25	562
Catherine Metaxotou Greece	12	130 0.5×	188 0.9×	140 1.0×	36 0.4×	10 0.2×	35	334
Michelle Merrill United States	6	261 1.0×	295 1.4×	331 2.4×	17 0.2×	68 1.4×	8	629
Yaoyong Chen China	13	432 1.7×	98 0.5×	31 0.2×	30 0.3×	25 0.5×	22	521
Tamar Schwartz Israel	11	273 1.1×	136 0.6×	103 0.8×	29 0.3×	97 1.9×	18	481

Countries citing papers authored by Chiara Palka

Since Specialization

Citations

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

Fields of papers citing papers by Chiara Palka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Palka

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Palka. A scholar is included among the top collaborators of Chiara Palka 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 Chiara Palka. Chiara Palka 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

Minelli, M., Chiara Palka, Elisena Morizio, et al.. (2025). 1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case. Current Issues in Molecular Biology. 47(1). 26–26.

Baig, Ammad A., Mariusz Kruk, James Im, et al.. (2023). O-005 Submaximal angioplasty alone vs. stenting plus angioplasty for symptomatic intracranial atherosclerotic disease – a propensity score matched comparative study with long term follow-up. A5.1–A5.

Palka, Chiara, Paolo Guanciali‐Franchi, Elisena Morizio, et al.. (2019). Non-invasive prenatal screening: A 20-year experience in Italy. European Journal of Obstetrics & Gynecology and Reproductive Biology X. 3. 100050–100050. 3 indexed citations

Franchi, Paolo Guanciali, Chiara Palka, Elisena Morizio, et al.. (2017). Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis. PLoS ONE. 12(12). e0189235–e0189235. 10 indexed citations

Guanciali‐Franchi, Paolo, et al.. (2016). An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations. Molecular Syndromology. 8(1). 42–44.

Verrotti, Alberto, Chiara Palka, Giovanni Prezioso, et al.. (2015). Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures. Cytogenetic and Genome Research. 146(2). 115–119. 9 indexed citations

Gatta, Valentina, Chiara Palka, Valentina Chiavaroli, et al.. (2014). Spectrum of phenotypic anomalies in four families with deletion of the SHOX enhancer region. BMC Medical Genetics. 15(1). 87–87. 6 indexed citations

Palka, Chiara, Elisena Morizio, Valentina Gatta, et al.. (2013). De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. Clinical Dysmorphology. 22(3). 132–134. 1 indexed citations

Palka, Chiara, Valentina Gatta, Antonio Novelli, et al.. (2012). 16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. Gene. 498(2). 328–331. 9 indexed citations

10.

Palka, Chiara, Stefania De Marco, Valentina Chiavaroli, et al.. (2012). Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. Gene. 504(1). 107–110. 6 indexed citations

11.

Palka, Chiara, Ivana Antonucci, Angelika Mohn, et al.. (2012). Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH. Clinical Dysmorphology. 21(3). 137–140. 1 indexed citations

12.

Palka, Chiara, Elisena Morizio, Valentina Gatta, et al.. (2011). A New Case of Pure Partial 7q Duplication. Cytogenetic and Genome Research. 136(1). 1–5. 23 indexed citations

13.

Guanciali‐Franchi, Paolo, Chiara Palka, Barbara Matarrelli, et al.. (2011). Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high‐risk pregnant women. Prenatal Diagnosis. 31(11). 1077–1081. 7 indexed citations

14.

Raicu, Florina, Valentina Gatta, Chiara Palka, et al.. (2008). Novel mutation in the ligand-binding domain of the androgen receptor gene (1790p) associated with complete androgen insensitivity syndrome. Asian Journal of Andrology. 10(4). 687–691. 7 indexed citations

15.

Guanciali‐Franchi, Paolo, Giuseppe Calabrese, Elisena Morizio, et al.. (2008). A new case of mosaicism for invdup(15) duplicated for Prader–Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. European Journal of Medical Genetics. 51(3). 239–244.

16.

Bernardini, Laura, Chiara Palka, Anna Capalbo, et al.. (2007). Complex rearrangement of chromosomes 7q21.13‐q22.1 confirms the ectrodactyly‐deafness locus and suggests new candidate genes. American Journal of Medical Genetics Part A. 146A(2). 238–244. 28 indexed citations

17.

Scarciolla, Oronzo, Liborio Stuppia, Maria Vittoria De Angelis, et al.. (2006). Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification. Neurogenetics. 7(4). 269–276. 59 indexed citations

18.

Gatta, Valentina, Ivana Antonucci, Elisena Morizio, et al.. (2006). Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay. Journal of Human Genetics. 52(1). 21–27. 27 indexed citations

19.

Gatta, Valentina, Oronzo Scarciolla, Chiara Palka, et al.. (2005). Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). Human Genetics. 117(1). 92–98. 88 indexed citations

20.

Celentano, Claudio, Paolo Guanciali‐Franchi, Marco Liberati, et al.. (2005). Lack of correlation between elevated maternal serum hCG during second‐trimester biochemical screening and fetal congenital anomaly. Prenatal Diagnosis. 25(3). 220–224. 3 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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