V. Ventruto

1.1k citations

48 papers · 792 indexed · h-index 17

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

Co-authors: Barkur S. Shastry Xiaodong Jiao J. Fielding Hejtmancik Michael T. Trese Corrado Baglioni M Stabile Michele D’Urso Maria Giuseppina Miano
Topics: Hemoglobinopathies and Related Disorders (8 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers)Genomic variations and chromosomal abnormalities (5 papers)
Cited by: Developmental Biology Genetics
Journals: Science Annals of the New York Academy of Sciences The American Journal of Human Genetics
Partner nations: Italy United States Spain

In The Last Decade

V. Ventruto

46 papers receiving 756 citations

Peers

Countries citing papers authored by V. Ventruto

Since Specialization

Citations

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

Fields of papers citing papers by V. Ventruto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Ventruto

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

#	Work	Indexed citations
1	Severe Myopia with Unusual Retinal Anomalies and Dandy-Walker Sequence in Two Sibs. A Distinct New Neuro-ocular Disorder 2013 ·Ophthalmic Genetics ·Giuseppe de Crecchio,Gilda Cennamo,Nicole de Leeuw,(unknown),(unknown),(unknown),V. Ventruto	3
2	MRX87 family with Aristaless Xdup24bp mutation and implication for polyAlanine expansions 2007 ·BMC Medical Genetics ·(unknown),L. Spizzichino,Pio D’Adamo,Jlenia Monfregola,(unknown),Angela D’Eustacchio,V. Ventruto,Giovanni Neri,Michele D’Urso,Pietro Chiurazzi,Matilde Valeria Ursini,Maria Giuseppina Miano	23
3	Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2–q28 associated with ovarian dysfunction 2005 ·Human Reproduction ·(unknown),(unknown),Geppino Falco,V. Ventruto,Michele D’Urso,Matilde Valeria Ursini,Maria Giuseppina Miano	24
4	Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5 2004 ·The American Journal of Human Genetics ·Xiaodong Jiao,V. Ventruto,Michael T. Trese,Barkur S. Shastry,J. Fielding Hejtmancik	152
5	Mapping of MRX81 in Xp11.2‐Xq12 suggests the presence of a new gene involved in nonspecific X‐linked mental retardation 2003 ·American Journal of Medical Genetics Part A ·Ida Annunziata,Carmela Lanzara,Iván Conte,Alberto Zullo,V. Ventruto,Maria Michela Rinaldi,Michele D’Urso,Giorgio Casari,Alfredo Ciccodicola,Maria Giuseppina Miano	10
6	A t(2;8) Balanced Translocation with Breakpoints Near the Human HOXD Complex Causes Mesomelic Dysplasia and Vertebral Defects 2002 ·Genomics ·François Spitz,Thomas Montavon,(unknown),Michael A. Morris,(unknown),Stylianos E. Antonarakis,V. Ventruto,Denis Duboule	36
7	Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains 2001 ·Human Mutation ·Maria Giuseppina Miano,Francesco Testa,Francesco Filippini,(unknown),Iván Conte,Carmela Lanzara,José M. Millán,Carmelilia De Bernardo,Barbara Grammatico,Massimo Mangino,Isabella Torrente,Romeo Carrozzo,Francesca Simonelli,E. Rinaldi,V. Ventruto,Michele D’Urso,Carmen Ayuso,Alfredo Ciccodicola	34
8	Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa 1999 ·European Journal of Human Genetics ·Maria Giuseppina Miano,Francesco Testa,Maria Strazzullo,(unknown),Carmelilia De Bernardo,Barbara Grammatico,Francesca Simonelli,Massimo Mangino,Isabella Torrente,Giulio Ruberto,Magdalena Beneyto,Guillermo Antiñolo,E. Rinaldi,Cesare Danesino,V. Ventruto,Michele D’Urso,Carmen Ayuso,M. Baiget,Alfredo Ciccodicola	29
9	The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32 1998 ·Journal of Human Genetics ·Masahiro Fujimoto,Piranit Nik Kantaputra,Shiro Ikegawa,Yoshimitsu Fukushima,(unknown),Masafumi Matsuo,Takafumi Ishida,Tadashi Matsumoto,Shinji Kondo,Hiroaki Tomita,Han‐Xiang Deng,Michele D’Urso,Maria Michela Rinaldi,V. Ventruto,Toshihisa Takagi,Yusuke Nakamura,Norio Niikawa	31
10	A further observation of corneal dystrophy and perceptive deafness in two siblings 1997 ·Ophthalmic Genetics ·Adriano Magli,Luigi Capasso,(unknown),Vittorio Maurino,V. Ventruto	7
11	Simultaneous occurrence of tetrasomy 21 and trisomy 8 in a patient with early blastic metamorphosis of chronic myeloproliferative disorder 1995 ·American Journal of Hematology ·(unknown),Felicetto Ferrara,(unknown),(unknown),Luigi Del Vecchio,Fabrizio Pane,(unknown),R Cimino,Francesco Salvatore,V. Ventruto	8
12	Neu‐Laxova syndrome: Pathological, radiological, and prenatal findings in a stillborn female 1989 ·American Journal of Medical Genetics ·Rosa Russo,Maria DʼArmiento,Pasquale Martinelli,V. Ventruto,Giovanni Neri,James F. Reynolds	22
13	Prenatal ultrasound diagnosis of macroglossia in the Wiedemann‐Beckwith syndrome 1988 ·Prenatal Diagnosis ·Giovanni Cobellis,(unknown),M Stabile,Fortunato Lonardo,(unknown),(unknown),V. Ventruto	20
14	Familial Laryngeal Abductor Paralysis with Presumed Autosomal Dominant Inheritance 1982 ·Annals of Otology Rhinology & Laryngology ·(unknown),(unknown),(unknown),(unknown),V. Ventruto,(unknown)	16
15	t(21q21q)/r[t(21q21q)] mosaic in two unrelated patients with mild stigmata of Down's syndrome. 1982 ·PubMed ·Bruno Dallapiccola,I Bianco,(unknown),(unknown),Gioacchino Scarano,(unknown),M Stabile,V. Ventruto	8
16	Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter. 1980 ·PubMed ·Livio Pagano,G Fioretti,(unknown),(unknown),(unknown),Antonio Celona,(unknown),A Rinaldi,V. Ventruto	4
17	H-Y Antigen: Expression in Human Subjects with the Testicular Feminization Syndrome 1977 ·Science ·Gloria C. Koo,Stephen S. Wachtel,Paul Saenger,Maria I. New,Harvey Dosik,Anthony P. Amarose,Elizabeth Dorus,V. Ventruto	16
18	Hemoglobin Lepore: Its significance for thalassemia and clinical manifestations 1974 ·Annals of Hematology ·(unknown),V. Ventruto	6
19	Hemoglobinopathies in Campania with particular reference to the rare and new types 1970 ·Annals of Hematology ·(unknown),V. Ventruto,(unknown)	4
20	Two New Thalassaemic Syndromes: a) Homozygous Alpha-Thalassaemia. b) Cooley-Like Disease due to Homozygous Elevated Hb A<sub>2</sub> Without Microcythaemia 1964 ·Acta Haematologica ·(unknown),E Dini,V. Ventruto	2

About V. Ventruto

V. Ventruto is a scholar working on Developmental Biology, Genetics and Genetics, having authored 48 papers that have together received 792 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Developmental Biology (52 citations), Genetics (288 citations) and Genetics (81 citations). V. Ventruto has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Barkur S. Shastry, Xiaodong Jiao, J. Fielding Hejtmancik, Michael T. Trese, Corrado Baglioni, M Stabile, Michele D’Urso, Maria Giuseppina Miano, Maria Luigia Cavaliere and Gioacchino Scarano. Their work appears in journals such as Science, Annals of the New York Academy of Sciences and The American Journal of Human Genetics.

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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