Elisena Morizio

1.3k citations

53 papers · 907 indexed · h-index 20

Molecular Biology
Genetics top 5%
Pediatrics, Perinatology and Child Health top 10%
Hematology top 10%
Genetics top 10%

Co-authors: Giandomenico Palka Liborio Stuppia Giuseppe Calabrese G Calabrese Valentina Gatta Paolo Guanciali Franchi Rita Mingarelli Rita Peila
Topics: Genomic variations and chromosomal abnormalities (18 papers)Prenatal Screening and Diagnostics (14 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers)
Cited by: Genetics Hematology
Journals: PLoS ONE PEDIATRICS Nutrients
Partner nations: Italy United States France

In The Last Decade

Elisena Morizio

49 papers receiving 849 citations

Peers

Countries citing papers authored by Elisena Morizio

Since Specialization

Citations

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

Fields of papers citing papers by Elisena Morizio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisena Morizio

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	1q21.1 Duplication Syndrome and Anorectal Malformations: A Literature Review and a New Case 2025 ·Current Issues in Molecular Biology ·M. Minelli,Chiara Palka,(unknown),(unknown),Elisena Morizio,(unknown),Gabriele Lisi,Liborio Stuppia,Valentina Gatta	0
2	Non-invasive prenatal screening: A 20-year experience in Italy 2019 ·European Journal of Obstetrics & Gynecology and Reproductive Biology X ·Chiara Palka,Paolo Guanciali‐Franchi,Elisena Morizio,(unknown),(unknown),(unknown),Giandomenico Palka,Giuseppe Calabrese,Peter Benn	3
3	Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 2017 ·PLoS ONE ·Paolo Guanciali Franchi,Chiara Palka,Elisena Morizio,(unknown),(unknown),Donatella Fantasia,(unknown),Peter Benn,Giuseppe Calabrese	10
4	De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects 2013 ·Clinical Dysmorphology ·(unknown),Chiara Palka,Elisena Morizio,Valentina Gatta,Ivana Antonucci,(unknown),Francesco Chiarelli,Liborio Stuppia,Giandomenico Palka,Giuseppe Calabrese	1
5	A New Case of Pure Partial 7q Duplication 2011 ·Cytogenetic and Genome Research ·(unknown),Chiara Palka,Elisena Morizio,Valentina Gatta,(unknown),Paolo Guanciali Franchi,Robert Zori,Giuseppe Calabrese,Giandomenico Palka,Francesco Chiarelli	23
6	A new case of mosaicism for invdup(15) duplicated for Prader–Willi/Angelman syndrome critical region (PWACR) in an adult healthy man 2008 ·European Journal of Medical Genetics ·Paolo Guanciali‐Franchi,Giuseppe Calabrese,Elisena Morizio,Valentina Gatta,Chiara Palka,Liborio Stuppia,Orsetta Zuffardi	0
7	Lack of correlation between elevated maternal serum hCG during second‐trimester biochemical screening and fetal congenital anomaly 2005 ·Prenatal Diagnosis ·Claudio Celentano,Paolo Guanciali‐Franchi,Marco Liberati,Chiara Palka,Donatella Fantasia,Elisena Morizio,Giuseppe Calabrese,Liborio Stuppia,Siegfried Rotmensch	3
8	Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis 2004 ·American Journal of Medical Genetics Part A ·Paolo Guanciali‐Franchi,Giuseppe Calabrese,Elisena Morizio,Donatella Fantasia,Alessia Colosimo,Maria Michela Rinaldi,(unknown),(unknown),Fortunato Lonardo,(unknown),Adriana Zatterale,Carmelo Laganà,Liborio Stuppia,Giuseppe Sabatino,Giandomenico Palka	17
9	Inositide-specific phospholipase c β1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia 2004 ·Leukemia ·Vincenza Rita Lo Vasco,G Calabrese,Lucia Manzoli,Giandomenico Palka,Antonio Spadano,Elisena Morizio,Paolo Guanciali‐Franchi,Donatella Fantasia,Lucio Cocco	48
10	Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene 2004 ·Genomics ·Liborio Stuppia,Valentina Gatta,Oronzo Scarciolla,Ivana Antonucci,Elisena Morizio,Giuseppe Calabrese,Giandomenico Palka	3
11	C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 2002 ·European Journal of Human Genetics ·Liborio Stuppia,Valentina Gatta,(unknown),Ivana Antonucci,Elisena Morizio,Giuseppe Calabrese,Giandomenico Palka	67
12	Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation 2000 ·Bone Marrow Transplantation ·G Calabrese,Donatella Fantasia,(unknown),Elisena Morizio,Liborio Stuppia,Valentina Gatta,P Olioso,Rita Mingarelli,Antonio Spadano,Giandomenico Palka	7
13	Characterization of novel genes in AZF regions 2000 ·Journal of Endocrinological Investigation ·Liborio Stuppia,Valentina Gatta,Isabella Fogh,(unknown),Rossella Grande,Elisena Morizio,Donatella Fantasia,Antonio Pizzuti,G Calabrese,Giandomenico Palka	6
14	A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 1998 ·Human Genetics ·Liborio Stuppia,Valentina Gatta,(unknown),Paolo Guanciali Franchi,Elisena Morizio,(unknown),Rita Mingarelli,Vincenzo Sforza,Giovanni Vanni Frajese,R. Tenaglia,Giandomenico Palka	73
15	p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 1997 ·Cancer Genetics and Cytogenetics ·Liborio Stuppia,Giuseppe Calabrese,Rita Peila,Paolo Guanciali‐Franchi,Elisena Morizio,Antonio Spadano,Giandomenico Palka	41
16	Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis 1996 ·Cancer Genetics and Cytogenetics ·G Calabrese,Toon Min,Liborio Stuppia,R Powles,John Swansbury,Elisena Morizio,Rita Peila,Emilio Donti,Giuseppe Fioritoni,Giandomenico Palka	19
17	Duplication Xp22.2 and pseudoisodicentric Yq detected by FISH and PCR in a sterile male 1995 ·Clinical Genetics ·Giandomenico Palka,G Calabrese,Rita Mingarelli,P. Guanciali Franchi,Liborio Stuppia,Elisena Morizio,Rita Peila,Adriano Torres Antonucci	3
18	A woman with an apparent non‐mosaic 45,X delivered a 46,X,der(X) liveborn female 1994 ·Clinical Genetics ·Giandomenico Palka,Giuseppe Calabrese,Liborio Stuppia,P. Guanciali Franchi,Elisena Morizio,Rita Peila,Adriano Torres Antonucci	25
19	Assignment of the β-Arrestin 1 Gene (ARRB1) to Human Chromosome 11q13 1994 ·Genomics ·Giuseppe Calabrese,Michele Sallese,Anna Stornaiuolo,Elisena Morizio,Giandomenico Palka,Antonio De Blasi	11
20	Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysis 1994 ·Cancer Genetics and Cytogenetics ·Giuseppe Calabrese,Liborio Stuppia,Paolo Guanciali Franchi,Rita Peila,Elisena Morizio,A. M. Liberati,Antonio Spadano,Roberto Di Lorenzo,Emilio Donti,Adriano Torres Antonucci,Giandomenico Palka	39

About Elisena Morizio

Elisena Morizio is a scholar working on Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 53 papers that have together received 907 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). The work is most often cited by research in Genetics (396 citations), Hematology (140 citations) and Genetics (116 citations). Elisena Morizio has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Giandomenico Palka, Liborio Stuppia, Giuseppe Calabrese, G Calabrese, Valentina Gatta, Paolo Guanciali Franchi, Rita Mingarelli, Rita Peila, Donatella Fantasia and Ivana Antonucci. Their work appears in journals such as PLoS ONE, PEDIATRICS and Nutrients.

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.

Explore authors with similar magnitude of impact