HG Brunner

3.0k total citations
17 papers, 525 citations indexed

About

HG Brunner is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, HG Brunner has authored 17 papers receiving a total of 525 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cognitive Neuroscience. Recurrent topics in HG Brunner's work include Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (3 papers) and Mitochondrial Function and Pathology (2 papers). HG Brunner is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetic Syndromes and Imprinting (3 papers) and Mitochondrial Function and Pathology (2 papers). HG Brunner collaborates with scholars based in Netherlands, United States and Germany. HG Brunner's co-authors include Martin Oti, Jacob W. IJdo, Jasper J. Saris, M.H. Breuning, P. Pearson, Stephen T. Reeders, G.J.B. van Ommen, David F. Callen, Tim P. Keith and Lau Blonden and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Nature Genetics.

In The Last Decade

HG Brunner

16 papers receiving 513 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
HG Brunner Netherlands	8	407	240	48	29	23	17	525
Jurjen W. Westra United States	14	457 1.1×	175 0.7×	77 1.6×	26 0.9×	30 1.3×	20	692
Jorge Urresti United States	8	459 1.1×	240 1.0×	15 0.3×	11 0.4×	27 1.2×	12	659
Ivan Limongelli Italy	11	187 0.5×	165 0.7×	5 0.1×	18 0.6×	16 0.7×	19	370
B. Houston United Kingdom	13	243 0.6×	82 0.3×	4 0.1×	10 0.3×	15 0.7×	39	558
Michol Crist United States	11	160 0.4×	98 0.4×	17 0.4×	24 0.8×	4 0.2×	21	348
Qing Ruan United States	13	487 1.2×	162 0.7×	33 0.7×	3 0.1×	14 0.6×	15	661
Erica Bello United Kingdom	6	259 0.6×	120 0.5×	21 0.4×	6 0.2×	8 0.3×	7	382
Chee‐Seng Ku Singapore	11	295 0.7×	402 1.7×	6 0.1×	32 1.1×	19 0.8×	14	661
Jonathan Adkins United States	9	240 0.6×	125 0.5×	7 0.1×	54 1.9×	45 2.0×	18	421
Bartholomew J. Naughton United States	8	269 0.7×	81 0.3×	13 0.3×	5 0.2×	30 1.3×	11	464

Countries citing papers authored by HG Brunner

Since Specialization

Citations

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

Fields of papers citing papers by HG Brunner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of HG Brunner

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

All Works

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17 of 17 papers shown

Brunner, HG, et al.. (2015). What Remains of the �Middle Molecule� Hypothesis Today?. Contributions to nephrology. 44. 14–39. 1 indexed citations

Silfhout, Anneke T. Vulto‐van, et al.. (2011). A 380-kb Duplication in 7p22.3 Encompassing the <b><i>LFNG</i></b> Gene in a Boy with Asperger Syndrome. Molecular Syndromology. 2(6). 245–250. 6 indexed citations

Egger, J.I.M., et al.. (2009). Psychiatric Profile in Rubinstein-Taybi Syndrome. Psychopathology. 43(1). 63–68. 18 indexed citations

Kleefstra, Tjitske, Anthony I. Magee, Gabriele Gillessen‐Kaesbach, et al.. (2006). Haploinsufficiency of the Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) gene causes the 9q subtelomeric deletion syndrome. European Journal of Human Genetics. 14. 89–89. 1 indexed citations

Feenstra, Ilse, HG Brunner, & Conny M.A. van Ravenswaaij. (2006). Cytogenetic genotype-phenotype studies: Improving genotyping, phenotyping and data storage. Cytogenetic and Genome Research. 115(3-4). 231–239. 10 indexed citations

Oti, Martin & HG Brunner. (2006). The modular nature of genetic diseases. Clinical Genetics. 71(1). 1–11. 308 indexed citations

Luijendijk, Mirjam W.J., T.J.R. van de Pol, Gerard van Duijnhoven, et al.. (2003). Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs☆. Genomics. 82(4). 480–490. 18 indexed citations

Tartaglia, Marco, Ernest L. Mehler, Richard M. Goldberg, et al.. (2001). Correction: Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome. Nature Genetics. 29(4). 491–491. 5 indexed citations

Bokhoven, Hans van, John A. McGrath, Jacopo Celli, et al.. (2000). P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation.. The American Journal of Human Genetics. 67(4). 41–41. 6 indexed citations

10.

Steensel, Maurice A. M. Van, et al.. (1999). Probing the Gene eXpression Database for candidate genes. European Journal of Human Genetics. 7(8). 910–919. 12 indexed citations

11.

Breuning, M.H., F.G.M. Snijdewint, HG Brunner, et al.. (1990). Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).. Journal of Medical Genetics. 27(10). 603–613. 53 indexed citations

12.

Smeets, H., et al.. (1989). MspI RFLP at 19cen–q12 identified by the anonymous DNA sequence pPM17.4 [D19S29]. Nucleic Acids Research. 17(8). 3324–3324. 2 indexed citations

13.

Smeets, H., Jan Schepens, M. Coerwinkel, et al.. (1989). TaqI RFLP at 19q13.1 identified by the anonymous DNA sequence p5B18 [D19S28]. Nucleic Acids Research. 17(8). 3325–3325. 3 indexed citations

14.

Wieringa, Bé, et al.. (1988). Genetic and physical demarcation of the locus for dystrophia myotonica.. PubMed. 48. 47–69. 15 indexed citations

15.

Breuning, M.H., HG Brunner, Jasper J. Saris, et al.. (1987). IMPROVED EARLY DIAGNOSIS OF ADULT POLYCYSTIC KIDNEY DISEASE WITH FLANKING DNA MARKERS. The Lancet. 330(8572). 1359–1361. 64 indexed citations

16.

Brunner, HG, et al.. (1982). Gesichtsfelduntersuchung mit dem Computer-Perimeter Octopus nach Lasertherapie bei Chorioretinitis centralis serosa (Typ I nach Wessing). Klinische Monatsblätter für Augenheilkunde. 181(11). 376–378. 3 indexed citations

17.

Frick, Paul J. & HG Brunner. (1964). Megaloblastäre Folsäuremangel-Anämie bei Hämochromatose¹. DMW - Deutsche Medizinische Wochenschrift. 89(4). 161–165.

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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