Inge Buntinx

504 total citations
12 papers, 360 citations indexed

About

Inge Buntinx is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Inge Buntinx has authored 12 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Inge Buntinx's work include Genetic Syndromes and Imprinting (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (2 papers). Inge Buntinx is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and RNA modifications and cancer (2 papers). Inge Buntinx collaborates with scholars based in Belgium and Netherlands. Inge Buntinx's co-authors include Joke Beuten, Oebele F. Brouwer, Hans Stroink, Kathelijne Mangelschots, J. P. Fryns, Raoul C. M. Hennekam, J. Gert van Dijk, W.O. Renier, Koos Zwinderman and Laura Laan and has published in prestigious journals such as Epilepsia, Genomics and Journal of Medical Genetics.

In The Last Decade

Inge Buntinx

12 papers receiving 347 citations

Peers

Countries citing papers authored by Inge Buntinx

Since Specialization

Citations

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

Fields of papers citing papers by Inge Buntinx

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inge Buntinx

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

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Evolution of Epilepsy and EEG Findings in Angelman Syndrome 1997 ·Epilepsia ·Laura Laan, W.O. Renier, Willem F. Arts, Inge Buntinx, (unknown), Hans Stroink, Joke Beuten, Koos Zwinderman, J. Gert van Dijk, Oebele F. Brouwer	102
2	Acute and Chronic Effect of Molsidomine Extended Release on Exercise Capacity in Patients with Stable Angina, a Double-Blind Cross-Over Clinical Trial Versus Placebo 1995 ·Journal of Cardiovascular Pharmacology ·R Messin, (unknown), (unknown), Inge Buntinx	18
3	Clinical profile of Angelman syndrome at different ages 1995 ·American Journal of Medical Genetics ·Inge Buntinx, Raoul C. M. Hennekam, Oebele F. Brouwer, Hans Stroink, Joke Beuten, Kathelijne Mangelschots, J. P. Fryns	110
4	Molecular study of chromosome 15 in 22 patients with Angelman syndrome 1993 ·Human Genetics ·Joke Beuten, Kathelijne Mangelschots, Inge Buntinx, Paul Coucke, Oebele F. Brouwer, Raoul C. M. Hennekam, Christine Van Broeckhoven, Patrick J. Willems	19
5	Localization of a Gene Responsible for Nonspecific Mental Retardation (MRX9) to the Pericentromeric Region of the X Chromosome 1993 ·Genomics ·P J Willems, Lieve Vits, Inge Buntinx, Peter Raeymaekers, Christine Van Broeckhoven, Berten Ceulemans	15
6	Two siblings with midline field defects and Hirschsprung disease: Variable expression of Toriello‐Carey or new syndrome? 1993 ·American Journal of Medical Genetics ·(unknown), Inge Buntinx, (unknown), (unknown), (unknown)	18
7	Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis 1992 ·Human Genetics ·Kathelijne Mangelschots, Bernadette Van Roy, Frank Speleman, Nadine Van Roy, J. Gheuens, Joke Beuten, Inge Buntinx, (unknown), (unknown), Jan E. Dumon, Berten Ceulemans, Patrick J. Willems	4
8	Acardiac amorphous twin with prune belly sequence in the co‐twin 1991 ·American Journal of Medical Genetics ·Inge Buntinx, (unknown), P. Buytaert, Jan E. Dumon	11
9	Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiency. 1991 ·Journal of Medical Genetics ·Inge Buntinx, Patrick J. Willems, Silja E.C. Spitaels, (unknown), Anne M. De Paepe, Jan E. Dumon	34
10	A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities. 1991 ·PubMed ·Inge Buntinx, (unknown), (unknown), Jan E. Dumon	4
11	Blepharophimosis, iris coloboma, microgenia, hearing loss, postaxial polydactyly, aplasia of corpus callosum, hydroureter, and developmental delay 1990 ·American Journal of Medical Genetics ·Inge Buntinx, Frank Majewski	13
12	A single maxillary incisor as a manifestation of an ectodermal dysplasia. 1989 ·Journal of Medical Genetics ·Inge Buntinx, M Baraitser	12

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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