Heidi G. Sutherland

5.2k total citations · 1 hit paper
95 papers, 3.8k citations indexed

About

Heidi G. Sutherland is a scholar working on Molecular Biology, Psychiatry and Mental health and Genetics. According to data from OpenAlex, Heidi G. Sutherland has authored 95 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 28 papers in Psychiatry and Mental health and 24 papers in Genetics. Recurrent topics in Heidi G. Sutherland's work include Migraine and Headache Studies (25 papers), Epigenetics and DNA Methylation (17 papers) and Genomics and Chromatin Dynamics (11 papers). Heidi G. Sutherland is often cited by papers focused on Migraine and Headache Studies (25 papers), Epigenetics and DNA Methylation (17 papers) and Genomics and Chromatin Dynamics (11 papers). Heidi G. Sutherland collaborates with scholars based in Australia, United Kingdom and United States. Heidi G. Sutherland's co-authors include Wendy A. Bickmore, Emma Whitelaw, David I. K. Martin, Hugh D. Morgan, Lyn R. Griffiths, Larisa M. Haupt, Cassie L. Albury, Graeme R. Grimes, Madapura M. Pradeepa and Jernej Ule and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Heidi G. Sutherland

90 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Epigenetic inheritance at the agouti locus in the mouse

1999 992 citations Heidi G. Sutherland, David I. K. Martin et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Heidi G. Sutherland Australia	24	2.5k	1.0k	477	385	301	95	3.8k
Giulio Genovese United States	33	2.6k 1.0×	1.8k 1.8×	362 0.8×	242 0.6×	228 0.8×	67	6.8k
Michel Guipponi Switzerland	32	2.1k 0.8×	931 0.9×	403 0.8×	195 0.5×	115 0.4×	87	3.7k
Christel Depienne France	33	1.1k 0.4×	836 0.8×	755 1.6×	234 0.6×	75 0.2×	98	3.2k
Sarven Sabunciyan United States	23	3.2k 1.3×	953 0.9×	155 0.3×	234 0.6×	184 0.6×	44	4.0k
Alexander G. Bassuk United States	37	2.4k 0.9×	1.0k 1.0×	145 0.3×	408 1.1×	69 0.2×	153	4.4k
Steven R. Grossman United States	45	4.8k 1.9×	1.1k 1.1×	329 0.7×	83 0.2×	122 0.4×	102	7.8k
D. Holmes Morton United States	39	2.5k 1.0×	925 0.9×	98 0.2×	487 1.3×	138 0.5×	76	4.7k
G Lucotte France	28	1.0k 0.4×	866 0.9×	189 0.4×	131 0.3×	224 0.7×	238	3.1k
Audrey C. Papp United States	33	1.7k 0.7×	444 0.4×	298 0.6×	328 0.9×	44 0.1×	57	3.9k
Mark Leppert United States	33	3.1k 1.2×	1.7k 1.6×	378 0.8×	309 0.8×	316 1.0×	63	5.9k

Countries citing papers authored by Heidi G. Sutherland

Since Specialization

Citations

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

Fields of papers citing papers by Heidi G. Sutherland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heidi G. Sutherland. 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 Heidi G. Sutherland. The network helps show where Heidi G. Sutherland may publish in the future.

Co-authorship network of co-authors of Heidi G. Sutherland

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

All Works

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20 of 20 papers shown

Maksemous, Neven, et al.. (2024). PathVar: A Customisable NGS Variant Calling Algorithm Implicates Novel Candidate Genes and Pathways in Hemiplegic Migraine. Clinical Genetics. 107(2). 157–168. 2 indexed citations

Maksemous, Neven, et al.. (2024). Targeted exonic sequencing identifies novel variants in a cerebral small vessel disease cohort. Clinica Chimica Acta. 567. 120120–120120. 1 indexed citations

Oikari, Lotta E., Heidi G. Sutherland, Dale R. Nyholt, et al.. (2024). CpG methylation changes in human mesenchymal and neural stem cells in response to in vitro niche modifications. Biochimie. 223. 147–157.

Sutherland, Heidi G., et al.. (2023). Association Study of a Comprehensive Panel of Neuropeptide-Related Polymorphisms Suggest Potential Roles in Verbal Learning and Memory. Genes. 15(1). 30–30.

Lea, Rod A., Neven Maksemous, Robert A. Smith, et al.. (2023). Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology. Human Genetics. 142(9). 1361–1373.

Benton, Miles C., Rod A. Lea, Heidi G. Sutherland, et al.. (2022). Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population. Scientific Reports. 12(1). 6827–6827. 9 indexed citations

Benton, Miles C., et al.. (2022). Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons. Journal of Forensic Sciences. 67(5). 1766–1775. 10 indexed citations

Lea, Rod A., Neven Maksemous, Robert A. Smith, et al.. (2022). Investigating a Genetic Link Between Alzheimer’s Disease and CADASIL-Related Cerebral Small Vessel Disease. Molecular Neurobiology. 59(12). 7293–7302. 4 indexed citations

Sutherland, Heidi G., et al.. (2021). Exploring the Hereditary Nature of Migraine. Neuropsychiatric Disease and Treatment. Volume 17. 1183–1194. 33 indexed citations

10.

Sutherland, Heidi G., et al.. (2020). Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach. Journal of Neurotrauma. 37(17). 1870–1879. 8 indexed citations

11.

Benton, Miles C., Heidi G. Sutherland, Donia Macartney‐Coxson, et al.. (2019). Methylome‐wide association study of whole blood DNA in the Norfolk Island isolate identifies robust loci associated with age. Figshare. 6 indexed citations

12.

Benton, Miles C., Robert A. Smith, Larisa M. Haupt, et al.. (2019). Variant Call Format–Diagnostic Annotation and Reporting Tool. Journal of Molecular Diagnostics. 21(6). 951–960. 8 indexed citations

13.

Sutherland, Heidi G., et al.. (2019). Saliva as a comparable-quality source of DNA for Whole Exome Sequencing on Ion platforms. Genomics. 112(2). 1437–1443. 4 indexed citations

14.

Albury, Cassie L., Neven Maksemous, Miles C. Benton, et al.. (2018). Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes. Frontiers in Genetics. 9. 20–20. 92 indexed citations

15.

Sutherland, Heidi G., Bridget H. Maher, Astrid J. Rodriguez‐Acevedo, Larisa M. Haupt, & Lyn R. Griffiths. (2014). Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraine. QUT ePrints (Queensland University of Technology). 4 indexed citations

16.

Sutherland, Heidi G., et al.. (2013). Studies on the Pathophysiology and Genetic Basis of Migraine. Current Genomics. 14(5). 300–315. 4 indexed citations

17.

Sutherland, Heidi G., et al.. (2003). 3D3/lyric: a novel transmembrane protein of the endoplasmic reticulum and nuclear envelope, which is also present in the nucleolus. Experimental Cell Research. 294(1). 94–105. 88 indexed citations

18.

Bickmore, Wendy A. & Heidi G. Sutherland. (2002). NEW EMBO MEMBER’S REVIEW: Addressing protein localization within the nucleus. The EMBO Journal. 21(10). 2507–2507. 4 indexed citations

19.

Sutherland, Heidi G.. (2001). Large-scale identification of mammalian proteins localized to nuclear sub-compartments. Human Molecular Genetics. 10(18). 1995–2011. 103 indexed citations

20.

Sutherland, Heidi G., David I. K. Martin, & Emma Whitelaw. (1997). A Globin Enhancer Acts by Increasing the Proportion of Erythrocytes Expressing a Linked Transgene. Molecular and Cellular Biology. 17(3). 1607–1614. 67 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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