Heinz Gabriel

669 total citations
15 papers, 308 citations indexed

About

Heinz Gabriel is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Heinz Gabriel has authored 15 papers receiving a total of 308 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Heinz Gabriel's work include Genomics and Rare Diseases (3 papers), Genetic and rare skin diseases. (3 papers) and Prenatal Screening and Diagnostics (3 papers). Heinz Gabriel is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic and rare skin diseases. (3 papers) and Prenatal Screening and Diagnostics (3 papers). Heinz Gabriel collaborates with scholars based in Germany, Serbia and Austria. Heinz Gabriel's co-authors include Klaus Jahnke, Elke Winterhager, Martin Genčík, Dušan Trpinac, Snežana Minić, Vincent Morinière, Sandrine Marlin, Estelle Colin, Laurence Heidet and Pauline Krug and has published in prestigious journals such as Blood, American Journal of Obstetrics and Gynecology and Journal of Clinical Pathology.

In The Last Decade

Heinz Gabriel

14 papers receiving 296 citations

Peers

Countries citing papers authored by Heinz Gabriel

Since Specialization

Citations

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

Fields of papers citing papers by Heinz Gabriel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heinz Gabriel

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Differenzierte Herangehensweise und Testung seltener genetischer Erkrankungen im Kindes- und Jugendalter 2023 ·Monatsschrift Kinderheilkunde ·Nadine Bachmann, Bernd Auber, Anibh M. Das, Felix Distelmaier, Heinz Gabriel, Nastassja Himmelreich, Johannes R. Lemke, Carsten Bergmann	0
2	Rare diseases: why is a rapid referral to an expert center so important? 2023 ·BMC Health Services Research ·(unknown), (unknown), Anne Pankow, Simon Ronicke, Heinz Gabriel, Annette D. Wagner	18
3	Should we offer prenatal exome sequencing for intrauterine growth restriction or short long bones? A systematic review and meta-analysis 2022 ·American Journal of Obstetrics and Gynecology ·Fionnuala Mone, Rhiannon Mellis, Heinz Gabriel, Caitlin Baptiste, Jessica L. Giordano, Ronald J. Wapner, Lyn S. Chitty	24
4	Germline Variants in MDM4 Cause a Disorder of p53 Dysregulation and Insufficient Telomere Maintenance 2022 ·Blood ·Robert Meyer, Matthias Begemann, (unknown), (unknown), (unknown), (unknown), Heinz Gabriel, (unknown), Margherita Vieri, Susanne Isfort, Martin Kirschner, Jens Panse, Udo Kontny, Selim Corbacioglu, Tim H. Brümmendorf, Ingo Kurth, Fabian Beier	1
5	Trio exome sequencing is highly relevant in prenatal diagnostics 2021 ·Prenatal Diagnosis ·Heinz Gabriel, (unknown), (unknown), (unknown), Florian Battke, Constantin von Kaisenberg, (unknown), (unknown), (unknown), Lutz Pfeiffer, Michael Entezami, Andreas Schröer, Joachim Bürger, Eva Maria Christina Schwaibold, (unknown), Saskia Biskup	35
6	Whole Exome Sequencing Revealed a Candidate Gene for Finkelstein-Seidlmayer Disease 2019 ·(unknown), Heinz Gabriel, Sebastiano A. G. Lava, Gian Paolo Ramelli, Manuel Luedeke, Saskia Biskup, Carlo Mainetti, Alessandra Ferrarini	3
7	Clubfoot associated with preaxial polydactyly 2014 ·Journal of Pediatric Orthopaedics B ·Oliver Eberhardt, Francisco Fernández Fernández, Heinz Gabriel, Thomas Wirth, Susanne Fuchs‐Winkelmann, Christian Dominik Peterlein	1
8	First IKBKG gene mutation study in Serbian incontinentia pigmenti patients 2013 ·Srpski arhiv za celokupno lekarstvo ·Snežana Minić, Dušan Trpinac, Heinz Gabriel, Martin Genčík, (unknown)	2
9	Dental and oral anomalies in incontinentia pigmenti: a systematic review 2012 ·Clinical Oral Investigations ·Snežana Minić, Dušan Trpinac, Heinz Gabriel, Martin Genčík, (unknown)	43
10	Hereditary Hyperferritinemia Cataract Syndrome: Clinical, Genetic, and Laboratory Findings in 5 Families 2011 ·Klinische Pädiatrie ·(unknown), Thorsten Langer, Holger Blessing, Heinz Gabriel, (unknown), (unknown), E. Kohne, Martin Genčík, Klaus‐Michael Debatin, Holger Cario	7
11	Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations 2010 ·Human Mutation ·Pauline Krug, Vincent Morinière, Sandrine Marlin, (unknown), Heinz Gabriel, Estelle Colin, Dominique Bonneau, Rémi Salomon, Corinne Antignac, Laurence Heidet	74
12	Incontinentia pigmenti with ultrastructurally disordered leucocytes 2010 ·Journal of Clinical Pathology ·Snežana Minić, Dušan Trpinac, M Obradović, G. E. K. Novotny, Heinz Gabriel, Marius Kuhn	3
13	Unique occurrence of Brachmann-de lange syndrome in a fetus whose mother presented with a diffuse large B-cell lymphoma 2007 ·Pathology & Oncology Research ·(unknown), Monika Schiesser, (unknown), Gholamali Tariverdian, (unknown), Heinz Gabriel, Gregor Mikuz, Consolato Sergi	1
14	Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population 2001 ·Human Mutation ·Heinz Gabriel, (unknown), (unknown), Elke Winterhager, Klaus Jahnke, (unknown)	89
15	Amyloidosis cutis nodularis atrophicans 1957 ·Dermatology ·Heinz Gabriel, (unknown)	7

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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