HG Brunner

1.0k total citations
10 papers, 531 citations indexed

About

HG Brunner is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, HG Brunner has authored 10 papers receiving a total of 531 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in HG Brunner's work include Genomics and Rare Diseases (3 papers), Muscle Physiology and Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). HG Brunner is often cited by papers focused on Genomics and Rare Diseases (3 papers), Muscle Physiology and Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). HG Brunner collaborates with scholars based in Netherlands, United States and Australia. HG Brunner's co-authors include Hans van Bokhoven, J. van Reeuwijk, Marjolein Visser, Egbert Bakker, Salvatore Seminara, W F Crowley, Naoko Sato, Jorieke E. H. Bergman, Tsutomu Ogata and Nelly Pitteloud and has published in prestigious journals such as The Lancet, Clinical Genetics and Health Physics.

In The Last Decade

HG Brunner

10 papers receiving 523 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	10	323	152	137	97	67	10	531
Elisabetta Pelo Italy	11	216 0.7×	80 0.5×	52 0.4×	50 0.5×	36 0.5×	36	480
John Bicknell United Kingdom	15	320 1.0×	60 0.4×	201 1.5×	27 0.3×	74 1.1×	18	853
Kyriaki S. Alatzoglou United Kingdom	15	334 1.0×	327 2.2×	68 0.5×	50 0.5×	54 0.8×	23	821
Oronzo Scarciolla Italy	10	222 0.7×	71 0.5×	123 0.9×	50 0.5×	25 0.4×	12	386
Jesse J. Savage United States	12	301 0.9×	213 1.4×	92 0.7×	22 0.2×	30 0.4×	23	658
Amanda H. Mortensen United States	13	364 1.1×	235 1.5×	36 0.3×	30 0.3×	50 0.7×	23	676
Louise Gregory United Kingdom	14	224 0.7×	171 1.1×	58 0.4×	22 0.2×	35 0.5×	25	520
Georgiann Baker United States	12	140 0.4×	84 0.6×	36 0.3×	28 0.3×	80 1.2×	21	526
J.H.A.M. Tuerlings Netherlands	18	440 1.4×	453 3.0×	76 0.6×	53 0.5×	210 3.1×	49	880
Ndona N. Nsumu United States	11	440 1.4×	47 0.3×	72 0.5×	24 0.2×	33 0.5×	12	585

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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10 of 10 papers shown

Mazzeu, Juliana F., Ana Cristina Victorino Krepischi, Astrid Oudakker, et al.. (2010). Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome. Clinical Genetics. 77(4). 404–407. 9 indexed citations

Reeuwijk, J. van, Christa van den Elzen, O.F. Brouwer, et al.. (2010). A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum. Clinical Genetics. 78(3). 275–281. 31 indexed citations

Beunders, Gea, Martin Callaghan, Nicole de Leeuw, et al.. (2010). Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions. Clinical Genetics. 80(1). 31–38. 21 indexed citations

Ben‐Shachar, Shay, et al.. (2009). Dominant versus recessive traits conveyed by allelic mutations – to what extent is nonsense‐mediated decay involved?. Clinical Genetics. 75(4). 394–400. 20 indexed citations

Pitteloud, Nelly, Tsutomu Ogata, Naoko Sato, et al.. (2008). CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome. Clinical Genetics. 75(1). 65–71. 150 indexed citations

Kleefstra, Tjitske, et al.. (2007). Pure subtelomeric microduplications as a cause of mental retardation. Clinical Genetics. 72(4). 362–368. 24 indexed citations

Reeuwijk, J. van, HG Brunner, & Hans van Bokhoven. (2004). Glyc‐O‐genetics of Walker–Warburg syndrome. Clinical Genetics. 67(4). 281–289. 72 indexed citations

Hoogerbrugge, Nicoline, et al.. (2002). Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCC. Clinical Genetics. 63(1). 64–70. 19 indexed citations

Bakker, Egbert, et al.. (1999). Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study. The Lancet. 353(9170). 2116–2119. 163 indexed citations

10.

Crameri, Reto, et al.. (1989). Indoor Rn Levels in Different Geological Areas in Switzerland. Health Physics. 57(1). 29–38. 22 indexed citations

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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