Michael S. Hildebrand

9.3k total citations
167 papers, 4.0k citations indexed

About

Michael S. Hildebrand is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Michael S. Hildebrand has authored 167 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 47 papers in Genetics and 39 papers in Sensory Systems. Recurrent topics in Michael S. Hildebrand's work include Hearing, Cochlea, Tinnitus, Genetics (39 papers), Genetics and Neurodevelopmental Disorders (31 papers) and Epilepsy research and treatment (21 papers). Michael S. Hildebrand is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (39 papers), Genetics and Neurodevelopmental Disorders (31 papers) and Epilepsy research and treatment (21 papers). Michael S. Hildebrand collaborates with scholars based in Australia, United States and Germany. Michael S. Hildebrand's co-authors include Richard J. Smith, A. Eliot Shearer, Ingrid E. Scheffer, Samuel F. Berkovic, Melanie Bahlo, Adam P. DeLuca, Hossein Najmabadi, John A. Damiano, Todd E. Scheetz and Hans‐Henrik M. Dahl and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Nature Communications.

In The Last Decade

Michael S. Hildebrand

159 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael S. Hildebrand Australia 36 1.6k 1.5k 854 628 497 167 4.0k
Agatino Battaglia Italy 38 1.6k 1.0× 285 0.2× 2.5k 2.9× 718 1.1× 409 0.8× 182 4.7k
Mei Zhang China 32 2.1k 1.3× 310 0.2× 237 0.3× 198 0.3× 402 0.8× 113 3.7k
Tracey A. Newman United Kingdom 31 855 0.5× 396 0.3× 162 0.2× 226 0.4× 1.1k 2.2× 74 3.8k
Laurent Nguyen Belgium 53 4.4k 2.8× 499 0.3× 773 0.9× 407 0.6× 357 0.7× 168 8.8k
Yin Yao Shugart United States 47 2.8k 1.8× 118 0.1× 2.2k 2.5× 704 1.1× 191 0.4× 153 6.8k
Sara Wells United Kingdom 29 1.7k 1.0× 157 0.1× 920 1.1× 123 0.2× 87 0.2× 94 3.6k
Heon Yung Gee South Korea 31 1.5k 0.9× 261 0.2× 691 0.8× 366 0.6× 133 0.3× 108 3.0k
Alfredo Ramı́rez Germany 32 2.0k 1.2× 325 0.2× 257 0.3× 186 0.3× 780 1.6× 126 4.7k
Andrea Gropman United States 38 2.8k 1.7× 121 0.1× 1.5k 1.8× 286 0.5× 103 0.2× 200 5.1k
Robin L. Davis United States 32 728 0.5× 980 0.6× 162 0.2× 645 1.0× 212 0.4× 80 2.8k

Countries citing papers authored by Michael S. Hildebrand

Since Specialization
Citations

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

Fields of papers citing papers by Michael S. Hildebrand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael S. Hildebrand. 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 Michael S. Hildebrand. The network helps show where Michael S. Hildebrand may publish in the future.

Co-authorship network of co-authors of Michael S. Hildebrand

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

All Works

20 of 20 papers shown
1.
Chiu, Annie Ting Gee, Mark F. Bennett, Amy Schneider, et al.. (2025). Pathogenic Variants in RNU2‐2 , a Non‐coding Spliceosomal RNA , Cause a Distinctive Developmental and Epileptic Encephalopathy. Annals of Neurology. 99(1). 51–58. 1 indexed citations
2.
Gambardella, Antonio, Yu‐Chi Liu, Mark F. Bennett, et al.. (2025). PAK3 pathogenic variant associated with sleep‐related hypermotor epilepsy in a family with parental mosaicism. Epilepsia Open. 10(2). 593–601.
3.
Kleinendorst, Lotte, Ozair Abawi, Niels Vos, et al.. (2024). GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical Obesity. 14(4). e12661–e12661.
4.
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.
5.
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
6.
Brown, Natasha J., M. De Silva, Mark F. Bennett, et al.. (2023). Improving genetic diagnostic yield in a large cohort of children with rare vascular anomalies or PIK3CA-related overgrowth spectrum. Genetics in Medicine Open. 2. 100837–100837.
7.
Bennett, Mark F., Ilka Immisch, Jeremy L. Freeman, et al.. (2023). Mosaic variants detectable in blood extend the clinicogenetic spectrum of GLI3-related hypothalamic hamartoma. SHILAP Revista de lepidopterología. 1(1). 100810–100810. 2 indexed citations
8.
Damiano, John A., Bronwyn E. Grinton, Patrick W. Carney, et al.. (2023). Recognition and epileptology of protracted CLN3 disease. Epilepsia. 64(7). 1833–1841. 2 indexed citations
9.
Haslam, Nick, Miriam A. Mosing, Michael S. Hildebrand, et al.. (2022). Genetic factors and shared environment contribute equally to objective singing ability. iScience. 25(6). 104360–104360. 7 indexed citations
10.
Fennell, Andrew, Samuel F. Berkovic, Carolyn Ellaway, et al.. (2022). The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American Journal of Medical Genetics Part A. 188(12). 3432–3447. 12 indexed citations
11.
Schimmel, Mareike, Susanna Schubert, Johannes R. Lemke, et al.. (2022). Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndrome. European Journal of Human Genetics. 30(3). 384–388. 6 indexed citations
12.
Ye, Zimeng, Mark F. Bennett, Andrew Neal, et al.. (2022). Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes. Neurology. 99(23). 1036–1041. 20 indexed citations
13.
Bagnall, Richard D., Mark F. Bennett, A. Marie Phillips, et al.. (2021). Loss‐of‐function variants in Kv11.1 cardiac channels as a biomarker for SUDEP. Annals of Clinical and Translational Neurology. 8(7). 1422–1432. 9 indexed citations
14.
MacGregor, Duncan, Susan M. Carden, Chelsee Hewitt, et al.. (2021). Identification of a recurrent mosaic KRAS variant in brain tissue from an individual with nevus sebaceous syndrome. Molecular Case Studies. 7(6). a006133–a006133. 6 indexed citations
15.
Sadleir, Lynette G., Guillem de Valles‐Ibáñez, Chontelle King, et al.. (2020). Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsy. Epilepsia. 61(4). e23–e29. 16 indexed citations
16.
Damiano, John A., Lucy Deng, Wenhui Li, et al.. (2019). SCN1A Variants in vaccine‐related febrile seizures: A prospective study. Annals of Neurology. 87(2). 281–288. 18 indexed citations
17.
Kınay, Demet, Karen Oliver, Erdem Tüzün, et al.. (2018). Evidence of linkage to chromosome 5p13.2‐q11.1 in a large inbred family with genetic generalized epilepsy. Epilepsia. 59(8). e125–e129. 1 indexed citations
18.
Smith, Richard J. & Michael S. Hildebrand. (2015). DFNA2 Nonsyndromic Hearing Loss. 1 indexed citations
19.
Grillet, Nicolas, Martin Schwander, Michael S. Hildebrand, et al.. (2009). Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans. The American Journal of Human Genetics. 85(3). 328–337. 110 indexed citations
20.
Hildebrand, Michael S., et al.. (2008). A novel splice site mutation in EYA4 causes DFNA10 hearing loss (vol 143, pg 1599, 2007). American Journal of Medical Genetics Part A. 2 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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