Ruth Braden

626 total citations
16 papers, 149 citations indexed

About

Ruth Braden is a scholar working on Genetics, Developmental and Educational Psychology and Molecular Biology. According to data from OpenAlex, Ruth Braden has authored 16 papers receiving a total of 149 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Developmental and Educational Psychology and 5 papers in Molecular Biology. Recurrent topics in Ruth Braden's work include Genetics and Neurodevelopmental Disorders (7 papers), Language Development and Disorders (7 papers) and Genomics and Rare Diseases (5 papers). Ruth Braden is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Language Development and Disorders (7 papers) and Genomics and Rare Diseases (5 papers). Ruth Braden collaborates with scholars based in Australia, United States and Netherlands. Ruth Braden's co-authors include Angela Morgan, David J. Amor, Hayley S. Mountford, Dianne F. Newbury, Simon E. Fisher, Siddharth Srivastava, Ingrid E. Scheffer, Bregje W.M. van Bon, Himanshu Goel and Estelle Colin and has published in prestigious journals such as Neurology, Developmental Medicine & Child Neurology and Journal of Medical Genetics.

In The Last Decade

Ruth Braden

13 papers receiving 149 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ruth Braden Australia	7	73	47	40	40	21	16	149
Miya St John Australia	7	65 0.9×	35 0.7×	30 0.8×	39 1.0×	16 0.8×	11	118
Natalia Freitas Rossi Brazil	10	66 0.9×	60 1.3×	42 1.1×	51 1.3×	27 1.3×	30	231
Claudia Rigamonti Italy	6	86 1.2×	31 0.7×	38 0.9×	59 1.5×	15 0.7×	15	129
Gérald Bussy France	8	80 1.1×	25 0.5×	70 1.8×	31 0.8×	7 0.3×	17	176
Paola Vizziello Italy	10	138 1.9×	58 1.2×	65 1.6×	96 2.4×	20 1.0×	31	265
Hope Sparks Lancaster United States	9	80 1.1×	153 3.3×	16 0.4×	98 2.5×	33 1.6×	20	264
Silvia Sacco France	8	54 0.7×	38 0.8×	41 1.0×	59 1.5×	7 0.3×	17	227
Alejandro Q. Nato United States	7	101 1.4×	29 0.6×	53 1.3×	35 0.9×	5 0.2×	17	167
Elizabeth R Hennessy Netherlands	5	141 1.9×	92 2.0×	66 1.6×	94 2.4×	22 1.0×	5	231
Douglas M. Shaw United States	8	35 0.5×	43 0.9×	44 1.1×	23 0.6×	44 2.1×	11	150

Countries citing papers authored by Ruth Braden

Since Specialization

Citations

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

Fields of papers citing papers by Ruth Braden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth Braden

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

All Works

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16 of 16 papers shown

Vogel, Adam P., John Christodoulou, Wendy Gold, et al.. (2025). Understanding speech and language in KIF1A-associated neurological disorder. European Journal of Human Genetics. 34(1). 78–89.

Vogel, Adam P., Michael Fahey, Ruth Braden, et al.. (2025). Speech, Language and Non‐verbal Communication in CLN2 and CLN3 Batten Disease. Journal of Inherited Metabolic Disease. 48(1). e12838–e12838. 2 indexed citations

Braden, Ruth, et al.. (2025). Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2 . American Journal of Medical Genetics Part A. 197(12). e64190–e64190.

Hildebrand, Michael S., Ruth Braden, Richard J. Leventer, et al.. (2024). Inherited PURA Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder. Neurology Genetics. 10(5). e200181–e200181. 4 indexed citations

Liégeois, Frédérique, Ruth Braden, Graeme D. Jackson, et al.. (2024). Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants. Neurology Genetics. 10(2). e200129–e200129.

Britten‐Jones, Alexis Ceecee, et al.. (2024). Clinician Awareness of Stickler Syndromes Among Australian Allied Health Care Professionals. Journal of Multidisciplinary Healthcare. Volume 17. 1755–1768. 1 indexed citations

Meng, Yan, Stephanie Best, David J. Amor, et al.. (2024). The value of genomic testing in severe childhood speech disorders. European Journal of Human Genetics. 32(4). 440–447. 6 indexed citations

Koene, Saskia, Dagmar Berghuis, Angela Morgan, et al.. (2023). Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of Medical Genetics. 61(4). 399–404. 4 indexed citations

Horton, Sarah, Victoria E. Jackson, Marie-Christine Franken, et al.. (2023). Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in Stuttering. Journal of Speech Language and Hearing Research. 67(10S). 4015–4024. 6 indexed citations

10.

Mountford, Hayley S., Ruth Braden, Dianne F. Newbury, & Angela Morgan. (2022). The Genetic and Molecular Basis of Developmental Language Disorder: A Review. Children. 9(5). 586–586. 27 indexed citations

11.

Braden, Ruth, et al.. (2022). Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments. European Journal of Human Genetics. 30(7). 800–811. 11 indexed citations

12.

Braden, Ruth, David J. Amor, Simon E. Fisher, et al.. (2021). Severe speech impairment is a distinguishing feature of FOXP1‐related disorder. Developmental Medicine & Child Neurology. 63(12). 1417–1426. 27 indexed citations

13.

Braden, Ruth, Siddharth Srivastava, Gaëtan Lesca, et al.. (2021). Clinical delineation of SETBP1 haploinsufficiency disorder. European Journal of Human Genetics. 29(8). 1198–1205. 17 indexed citations

14.

Morgan, Angela, Ruth Braden, Estelle Colin, et al.. (2021). Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European Journal of Human Genetics. 29(8). 1216–1225. 30 indexed citations

15.

Braden, Ruth, Chloe Stutterd, Kate Pope, et al.. (2021). Speech, Language, and Oromotor Skills in Patients With Polymicrogyria. Neurology. 96(14). e1898–e1912. 6 indexed citations

16.

Braden, Ruth, Richard J. Leventer, Anna Jansen, Ingrid E. Scheffer, & Angela Morgan. (2019). Speech and language in bilateral perisylvian polymicrogyria: a systematic review. Developmental Medicine & Child Neurology. 61(10). 1145–1152. 8 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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