Heidi G. Sutherland

5.2k citations

95 papers · 3.8k indexed · 1 hit paper · h-index 24

Molecular Biology top 2%
Genetics top 2%
Psychiatry and Mental health top 2%
Pediatrics, Perinatology and Child Health top 5%
Plant Science top 10%

Co-authors: Wendy A. Bickmore Emma Whitelaw David I. K. Martin Hugh D. Morgan Lyn R. Griffiths Larisa M. Haupt Cassie L. Albury Graeme R. Grimes
Topics: Migraine and Headache Studies (25 papers)Epigenetics and DNA Methylation (17 papers)Genomics and Chromatin Dynamics (11 papers)
Cited by: Virology Molecular Biology Genetics
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Nature Genetics
Partner nations: Australia United Kingdom United States

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

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

#	Work	Indexed citations
1	PathVar: A Customisable NGS Variant Calling Algorithm Implicates Novel Candidate Genes and Pathways in Hemiplegic Migraine 2024 ·Clinical Genetics ·(unknown),Neven Maksemous,Heidi G. Sutherland,Rod A. Lea,Lyn R. Griffiths	2
2	Targeted exonic sequencing identifies novel variants in a cerebral small vessel disease cohort 2024 ·Clinica Chimica Acta ·(unknown),Neven Maksemous,Robert A. Smith,Heidi G. Sutherland,Larisa M. Haupt,Lyn R. Griffiths	1
3	CpG methylation changes in human mesenchymal and neural stem cells in response to in vitro niche modifications 2024 ·Biochimie ·(unknown),Lotta E. Oikari,(unknown),Heidi G. Sutherland,Dale R. Nyholt,Lyn R. Griffiths,André J. van Wijnen,(unknown),Larisa M. Haupt	0
4	Association Study of a Comprehensive Panel of Neuropeptide-Related Polymorphisms Suggest Potential Roles in Verbal Learning and Memory 2023 ·Genes ·(unknown),Heidi G. Sutherland,Rod A. Lea,Larisa M. Haupt,David Shum,Lyn R. Griffiths	0
5	Exonic mutations in cell–cell adhesion may contribute to CADASIL-related CSVD pathology 2023 ·Human Genetics ·(unknown),Rod A. Lea,Neven Maksemous,Robert A. Smith,Heidi G. Sutherland,Larisa M. Haupt,Lyn R. Griffiths	0
6	Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population 2022 ·Scientific Reports ·(unknown),Miles C. Benton,Rod A. Lea,Heidi G. Sutherland,Janet Chaseling,Larisa M. Haupt,(unknown),Lyn R. Griffiths	9
7	Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons 2022 ·Journal of Forensic Sciences ·(unknown),Miles C. Benton,Rod A. Lea,Heidi G. Sutherland,Larisa M. Haupt,(unknown),Lyn R. Griffiths	10
8	Investigating a Genetic Link Between Alzheimer’s Disease and CADASIL-Related Cerebral Small Vessel Disease 2022 ·Molecular Neurobiology ·(unknown),Rod A. Lea,Neven Maksemous,Robert A. Smith,Heidi G. Sutherland,Larisa M. Haupt,Lyn R. Griffiths	4
9	Exploring the Hereditary Nature of Migraine 2021 ·Neuropsychiatric Disease and Treatment ·(unknown),Heidi G. Sutherland,Lyn R. Griffiths	33
10	Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach 2020 ·Journal of Neurotrauma ·(unknown),Heidi G. Sutherland,Neven Maksemous,Robert L. Smith,Larisa M. Haupt,Lyn R. Griffiths	8
11	Methylome‐wide association study of whole blood DNA in the Norfolk Island isolate identifies robust loci associated with age 2019 ·Figshare ·Miles C. Benton,Heidi G. Sutherland,Donia Macartney‐Coxson,Larisa M. Haupt,Rod A. Lea,Lyn R. Griffiths	6
12	Variant Call Format–Diagnostic Annotation and Reporting Tool 2019 ·Journal of Molecular Diagnostics ·Miles C. Benton,Robert A. Smith,Larisa M. Haupt,Heidi G. Sutherland,(unknown),Cassie L. Albury,Neven Maksemous,Rod A. Lea,Lyn R. Griffiths	8
13	Saliva as a comparable-quality source of DNA for Whole Exome Sequencing on Ion platforms 2019 ·Genomics ·(unknown),Heidi G. Sutherland,Larisa M. Haupt,Lyn R. Griffiths	4
14	Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes 2018 ·Frontiers in Genetics ·(unknown),Cassie L. Albury,Neven Maksemous,Miles C. Benton,Heidi G. Sutherland,Robert A. Smith,Larisa M. Haupt,Lyn R. Griffiths	92
15	Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraine 2014 ·QUT ePrints (Queensland University of Technology) ·Heidi G. Sutherland,Bridget H. Maher,Astrid J. Rodriguez‐Acevedo,Larisa M. Haupt,Lyn R. Griffiths	4
16	Studies on the Pathophysiology and Genetic Basis of Migraine 2013 ·Current Genomics ·(unknown),Heidi G. Sutherland,Lyn R. Griffiths	4
17	3D3/lyric: a novel transmembrane protein of the endoplasmic reticulum and nuclear envelope, which is also present in the nucleolus 2003 ·Experimental Cell Research ·Heidi G. Sutherland,Yun Wah Lam,(unknown),Angus I. Lamond,Wendy A. Bickmore	88
18	NEW EMBO MEMBER’S REVIEW: Addressing protein localization within the nucleus 2002 ·The EMBO Journal ·Wendy A. Bickmore,Heidi G. Sutherland	4
19	Large-scale identification of mammalian proteins localized to nuclear sub-compartments 2001 ·Human Molecular Genetics ·Heidi G. Sutherland	103
20	A Globin Enhancer Acts by Increasing the Proportion of Erythrocytes Expressing a Linked Transgene 1997 ·Molecular and Cellular Biology ·Heidi G. Sutherland,David I. K. Martin,Emma Whitelaw	67

About Heidi G. Sutherland

Heidi G. Sutherland is a scholar working on Psychiatry and Mental health, Endocrine and Autonomic Systems and Neurology, having authored 95 papers that have together received 3.8k indexed citations. Recurring topics across this work include Migraine and Headache Studies (25 papers), Epigenetics and DNA Methylation (17 papers) and Genomics and Chromatin Dynamics (11 papers). The work is most often cited by research in Virology (231 citations), Molecular Biology (2.5k citations) and Genetics (1.0k citations). Heidi G. Sutherland has collaborated with scholars based in Australia, United Kingdom and United States. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

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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