Constantinos Pángalos

1.0k citations

38 papers · 643 indexed · h-index 13

Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 16
Genetics top 10%
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 3
Hematology
- Acute Myeloid Leukemia Research 8
Genetics
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 3
Rheumatology
- Eosinophilic Disorders and Syndromes 3
Molecular Biology
- RNA modifications and cancer 4
Pulmonary and Respiratory Medicine
- Sarcoma Diagnosis and Treatment 3
Plant Science
- Chromosomal and Genetic Variations 3

Co-authors: Stylianos E. Antonarakis Dimitris Avramopoulos O Raoul Albert Schinzel J L Blouin Michael B. Petersen M Prieur Michael J. Hafez
Cited by: Pediatrics, Perinatology and Child Health Genetics Hematology
Journals: SHILAP Revista de lepidopterología (1 paper)Fertility and Sterility (1 paper)British Journal of Haematology (1 paper)
Partner nations: Greece United States France

In The Last Decade

Constantinos Pángalos

36 papers receiving 595 citations

Peers

Countries citing papers authored by Constantinos Pángalos

Since Specialization

Citations

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

Fields of papers citing papers by Constantinos Pángalos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Constantinos Pángalos, 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 Constantinos Pángalos Line = papers co-authored together Constantinos Pángalos links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The APOE E4 Allele Confers Increased Risk of Ischemic Stroke Among Greek Carriers Advances in Clinical and Experimental Medicine ·Christopher Konialis,Konstantinos Spengos,Panagiotis Iliopoulos,Sophia Karapanou,Elias Gialafos,Birgitta Hagnefelt,Konstantinos Vemmos,Nikolaos Zakopoulos,Constantinos Pángalos	2016	18
2	First applications of a targeted exome sequencing approach in fetuses with ultrasound abnormalities reveals an important fraction of cases with associated gene defects PeerJ ·Constantinos Pángalos,Birgitta Hagnefelt,Κωνσταντίνος Λιλάκος,Christopher Konialis	2016	43
3	Dilemmas in Prenatal Chromosomal Diagnosis Revealed Through a Single Center's 30 Years' Experience and 90,000 Cases Fetal Diagnosis and Therapy ·Christopher Konialis,Constantinos Pángalos,InterGenetics	2015	8
4	Resistin in mid-trimester amniotic fluid in trisomy 21 The Journal of Maternal-Fetal & Neonatal Medicine ·Nikolaos Vrachnis,L. Gkogkas,Stamatina Iliodromiti,C Grigoriadis,Evangelia Samoli,Zoi Iliodromiti,Constantinos Pángalos,Kalliopi I. Pappa,Nikolaos Drakoulis,George Creatsas,D. Botsis	2013	3
5	A familial case of Muenke syndrome. Diverse expressivity of theFGFR3Pro252Arg mutation – case report and review of the literature The Journal of Maternal-Fetal & Neonatal Medicine ·Christos Aravidis,Christopher Konialis,Constantinos Pángalos,Zoi Kosmaidou	2013	5
6	A Novel β⁰-Thalassemia Frameshift Mutation: [HBB:c.216delT] Hemoglobin ·Christopher Konialis,Birgitta Hagnefelt,Sophia Sevastidou,Katerina Pispili,Constantinos Pángalos	2012	1
7	Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non‐selective application of a MLPA‐based extended prenatal panel in routine prenatal diagnosis Prenatal Diagnosis ·Christopher Konialis,Birgitta Hagnefelt,Sophia Sevastidou,Sophia Karapanou,Katerina Pispili,Aggeliki Markaki,Constantinos Pángalos	2011	23
8	Successful Hematopoietic Stem Cell Transplantation in 2 Children with X-Linked Chronic Granulomatous Disease from Their Unaffected HLA-Identical Siblings Selected Using Preimplantation Genetic Diagnosis Combined with HLA Typing Biology of Blood and Marrow Transplantation ·Evgenios Goussetis,Christopher Konialis,Ioulia Peristeri,Vasiliki Kitra,Maria Dimopoulou,Theoni Petropoulou,George Vessalas,Andreas Papassavas,Marianna Tzanoudaki,Georgia Kokkali,Eftychia Petrakou,Antonia Spiropoulos,Constantinos Pángalos,Konstantinos Pantos,Stelios Graphakos	2009	20
9	Birth of a Healthy Histocompatible Sibling following Preimplantation Genetic Diagnosis for Chronic Granulomatous Disease at the Blastocyst Stage Coupled to HLA Typing Fetal Diagnosis and Therapy ·Constantinos Pángalos,Birgitta Hagnefelt,Georgia Kokkali,Konstantinos Pantos,Christopher Konialis	2008	10
10	Pregnancy following preimplantation genetic diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Prenatal Diagnosis ·Christopher Konialis,Birgitta Hagnefelt,Georgia Kokkali,Costas Pantos,Constantinos Pángalos	2007	7
11	Acute myelogenous leukemia with tetrasomy 8 is a disease with a poor prognosis Cancer Genetics and Cytogenetics ·Panagiotis Tsirigotis,Sotirios G. Papageorgiou,Danai Abatzis,Sofia Athanatou,Constantinos Girkas,Vasiliki Pappa,Constantinos Pángalos,E. Papageorgiou,John Dervenoulas,S. Raptis	2005	9
12	The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis Prenatal Diagnosis ·Aubrey Milunsky,Christopher Konialis,Sung Han Shim,Thomas A. Maher,K. Spengos,Masamichi Ito,Constantinos Pángalos	2005	7
13	Molecular analysis of transferrin receptor mRNA expression in acute myeloid leukaemia British Journal of Haematology ·Panagoula Κollia,Niki Stavroyianni,Κώστας Σταματόπουλος,Katerina Zoi,Nora‐Athina Viniou,Marina Mantzourani,Constance Tom Noguchi,George Paterakis,D Abazis,Constantinos Pángalos,Dimitris Loukopoulos,Xenophon Yataganas	2001	19
14	Acute Promyelocytic Leukemia Relapsing into FAB-M2 Acute Myeloid Leukemia with Trisomy 8 Cancer Genetics and Cytogenetics ·Niki Stavroyianni,Xenophon Yataganas,Danai Abazis,Constantinos Pángalos,John Meletis	2000	13
15	Cytogenetic Analysis and RAS Mutations in Primary Myelodysplastic Syndromes Cancer Genetics and Cytogenetics ·Eleni Plata,Nora Viniou,Danai Abazis,Kostas Konstantopoulos,Constantinos Troungos,George Vaiopoulos,John Meletis,Christos Kittas,Constantinos Pángalos,Xenophon Yataganas	1999	7
16	A novel chromosomal abnormality involving chromosomes 2 and 18 in a patient with myelodysplastic syndrome Cancer Genetics and Cytogenetics ·Nora Viniou,Danai Abazis,Xenophon Yataganas,Moncef Benkhalifa,Κώστας Σταματόπουλος,G. Vayopoulos,Eleni Plata,Dimitris Loukopoulos,Constantinos Pángalos	1997	1
17	Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter American Journal of Medical Genetics ·Catherine Sarri,Jolanda Gyftodimou,Dimitris Avramopoulos,Maria Grigoriadou,Winni Pedersen,Effie Pandelia,Constantinos Pángalos,D Abazis,George Kitsos,Dimitrios Vassilopoulos,Karen Brøndum‐Nielsen,Michael B. Petersen	1997	17
18	An unusual cytogenetic abnormality involving chromosomes 1 and 7 in a case of chronic myelomonocytic leukemia Cancer Genetics and Cytogenetics ·Stefanos I. Papadhimitriou,D Abazis,Constantina Repa,Christos Papaconstantinou,Constantinos Papanastasiou,Constantinos Pángalos,Marina Stamatelou	1995	2
19	Hypereosinophilia associated with monosomy 7 Cancer Genetics and Cytogenetics ·Nora Viniou,Xenophon Yataganas,D Abazis,George Paterakis,Stathis Vavourakis,Κώστας Σταματόπουλος,Marina Matzourani,Dimitris Loukopoulos,Constantinos Pángalos	1995	7
20	Pure partial trisomy of the short arm of chromosome 5 Human Genetics ·Marie Odile Rethoré,Marie Christine de Blois,Marie Peeters,P. Popowski,Constantinos Pángalos,J Lejeune	1989	32

About Constantinos Pángalos

Constantinos Pángalos is a scholar working on Pediatrics, Perinatology and Child Health, Hematology and Genetics, having authored 38 papers that have together received 643 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (12 papers), Acute Myeloid Leukemia Research (8 papers), RNA modifications and cancer (4 papers), Genetic Syndromes and Imprinting (3 papers), Eosinophilic Disorders and Syndromes (3 papers), Sarcoma Diagnosis and Treatment (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (297 citations), Genetics (337 citations) and Hematology (61 citations). Constantinos Pángalos has collaborated with scholars based in Greece, United States and France. Frequent co-authors include Stylianos E. Antonarakis, Dimitris Avramopoulos, O Raoul, Albert Schinzel, J L Blouin, Michael B. Petersen, M Prieur, Michael J. Hafez, Franz Binkert and Susan A. Slaugenhaupt. Their work appears in journals such as SHILAP Revista de lepidopterología, Fertility and Sterility and British Journal of Haematology.

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