Catherine Bromhead

2.9k total citations
8 papers, 287 citations indexed

About

Catherine Bromhead is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Catherine Bromhead has authored 8 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Neurology and 3 papers in Genetics. Recurrent topics in Catherine Bromhead's work include Hearing, Cochlea, Tinnitus, Genetics (2 papers), RNA modifications and cancer (2 papers) and Vestibular and auditory disorders (2 papers). Catherine Bromhead is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (2 papers), RNA modifications and cancer (2 papers) and Vestibular and auditory disorders (2 papers). Catherine Bromhead collaborates with scholars based in Australia, United States and Iran. Catherine Bromhead's co-authors include Melanie Bahlo, David J. Amor, Paul J. Lockhart, Martin B. Delatycki, Richard J. Leventer, Elizabeth Fitzpatrick, Katherine R. Smith, Richard J. Smith, Pleasantine Mill and Martin A.M. Reijns and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Genome biology.

In The Last Decade

Catherine Bromhead

8 papers receiving 274 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Catherine Bromhead Australia	8	169	150	41	37	36	8	287
Janice C. Palumbos United States	8	245 1.4×	161 1.1×	56 1.4×	32 0.9×	82 2.3×	13	391
L Korniszewski Poland	12	274 1.6×	249 1.7×	28 0.7×	85 2.3×	47 1.3×	26	498
Alisha Wilkens United States	13	239 1.4×	255 1.7×	104 2.5×	61 1.6×	34 0.9×	20	438
Muriel Holder France	9	283 1.7×	185 1.2×	18 0.4×	92 2.5×	22 0.6×	14	408
Érika L. Freitas Brazil	10	112 0.7×	122 0.8×	32 0.8×	31 0.8×	21 0.6×	16	260
R. Farcas Germany	6	210 1.2×	54 0.4×	22 0.5×	35 0.9×	24 0.7×	8	282
Jennifer McCallum United States	5	280 1.7×	112 0.7×	23 0.6×	41 1.1×	17 0.5×	5	355
Dinah Clark United States	15	495 2.9×	250 1.7×	57 1.4×	97 2.6×	54 1.5×	21	711
Jiale Xiang China	9	172 1.0×	88 0.6×	20 0.5×	85 2.3×	10 0.3×	24	345
Emmanuelle Ranza Switzerland	12	137 0.8×	103 0.7×	20 0.5×	11 0.3×	15 0.4×	22	295

Countries citing papers authored by Catherine Bromhead

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Bromhead

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Bromhead

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

Amor, David J., Ashley P.L. Marsh, Elsdon Storey, et al.. (2016). Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency. Neurology Genetics. 2(6). e114–e114. 16 indexed citations

Marsh, Ashley P.L., Vesna Lukić, Kate Pope, et al.. (2015). Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss. Neurology Genetics. 1(2). e16–e16. 25 indexed citations

Wilson, Gabrielle R., Katherine R. Smith, Kate Pope, et al.. (2013). Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. European Journal of Human Genetics. 22(6). 741–747. 30 indexed citations

Klein, Karl Martin, Catherine Bromhead, Katherine R. Smith, et al.. (2013). Autosomal dominant vasovagal syncope. Neurology. 80(16). 1485–1493. 17 indexed citations

Smith, Katherine R., Catherine Bromhead, Michael S. Hildebrand, et al.. (2011). Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes. Genome biology. 12(9). R85–R85. 50 indexed citations

Mill, Pleasantine, Paul J. Lockhart, Elizabeth Fitzpatrick, et al.. (2011). Human and Mouse Mutations in WDR35 Cause Short-Rib Polydactyly Syndromes Due to Abnormal Ciliogenesis. The American Journal of Human Genetics. 88(4). 508–515. 110 indexed citations

Hildebrand, Michael S., Kimia Kahrizi, Catherine Bromhead, et al.. (2010). Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population. Annals of Otology Rhinology & Laryngology. 119(12). 830–835. 24 indexed citations

Shearer, A. Eliot, Michael S. Hildebrand, Catherine Bromhead, et al.. (2009). A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. American Journal of Medical Genetics Part A. 149A(3). 555–558. 15 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.

Explore authors with similar magnitude of impact