Ian P. Blair

15.3k citations

97 papers · 6.0k indexed · 3 hit papers · h-index 31

Neurology top 0.1%
- Amyotrophic Lateral Sclerosis Research 66
- Neurological diseases and metabolism 20
- Parkinson's Disease Mechanisms and Treatments 20
Genetics top 0.2%
- Neurogenetic and Muscular Disorders Research 44
- Genetics and Neurodevelopmental Disorders 8
Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research 66
- Neurological diseases and metabolism 20
- Parkinson's Disease Mechanisms and Treatments 20
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders 11
- Genetic Neurodegenerative Diseases 10
Molecular Biology top 2%
- Prion Diseases and Protein Misfolding 8

Co-authors: Garth A. Nicholson Kelly L. Williams Jennifer C. Durnall Sadaf T. Warraich Christopher E. Shaw Caroline Vance Shu Yang P. Nigel Leigh
Cited by: Neurology Genetics
Journals: Science (1 paper)Nature Genetics (1 paper)Nature Neuroscience (1 paper)
Partner nations: Australia United States United Kingdom

In The Last Decade

Ian P. Blair

93 papers receiving 5.9k citations

Hit Papers

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Peers

Countries citing papers authored by Ian P. Blair

Since Specialization

Citations

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

Fields of papers citing papers by Ian P. Blair

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ian P. Blair. 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 Ian P. Blair. The network helps show where Ian P. Blair may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Ian P. Blair, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ian P. Blair Line = papers co-authored together Ian P. Blair links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement Molecular Neurodegeneration ·Natalie Grima,Andrew Smith,Claire E. Shepherd,Lyndal Henden,Thiri Zaw,Luke Carroll,Dominic B. Rowe,Matthew C. Kiernan,Ian P. Blair,Kelly L. Williams	2025	0
2	C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD Molecular Neurobiology ·Jessica Sultana,Audrey Ragagnin,Sonam Parakh,Sayanthooran Saravanabavan,Kai Y. Soo,Marta Vidal,Cyril J. Jagaraj,Kunjie Ding,Sharlynn Wu,Sina Shadfar,Emily K. Don,Anand K. Deva,Garth A. Nicholson,Dominic B. Rowe,Ian P. Blair,Shu Yang,Julie D. Atkin	2024	4
3	Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Lyndal Henden,Liam G. Fearnley,Dean Southwood,Andrew Smith,Dominic B. Rowe,Matthew C. Kiernan,Roger Pamphlett,Melanie Bahlo,Ian P. Blair,Kelly L. Williams	2024	0
4	ALS-linked CCNF variant disrupts motor neuron ubiquitin homeostasis Human Molecular Genetics ·Natalie E. Farrawell,Monique Bax,Luke McAlary,Jessie McKenna,Simon Maksour,Dzung Do‐Ha,Stephanie L. Rayner,Ian P. Blair,Roger S. Chung,Justin J. Yerbury,Lezanne Ooi,Darren N. Saunders	2023	4
5	Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants Journal of Neuromuscular Diseases ·Emily P. McCann,Natalie Grima,Jennifer A. Fifita,Sandrine Chan Moi Fat,Klaus Lehnert,Lyndal Henden,Ian P. Blair,Kelly L. Williams	2023	4
6	Association between DNA methylation variability and self-reported exposure to heavy metals Scientific Reports ·Anna Freydenzon,Marta F. Nabais,Tian Lin,Kelly L. Williams,Leanne Wallace,Anjali K. Henders,Ian P. Blair,Naomi R. Wray,Roger Pamphlett,Allan F. McRae	2022	10
7	NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk Neurobiology of Aging ·Natalie Grima,Lyndal Henden,Liam G. Fearnley,Dominic B. Rowe,Susan D’Silva,Roger Pamphlett,Lorel Adams,Matthew C. Kiernan,Srestha Mazumder,Hannah C. Timmins,Margaret Zoing,Melanie Bahlo,Ian P. Blair,Kelly L. Williams	2022	0
8	Sensitive Detection of Motor Neuron Disease Derived Exosomal miRNA Using Electrocatalytic Activity of Gold‐Loaded Superparamagnetic Ferric Oxide Nanocubes ChemElectroChem ·Mostafa Kamal Masud,Rabbee G. Mahmudunnabi,Nahian Binte Aziz,Claire H. Stevens,Dzung Do‐Ha,Shu Yang,Ian P. Blair,Md. Shahriar A. Hossain,Yoon‐Bo Shim,Lezanne Ooi,Yusuke Yamauchi,Muhammad J. A. Shiddiky	2020	20
9	Ubiquitin Homeostasis Is Disrupted in TDP-43 and FUS Cell Models of ALS iScience ·Natalie E. Farrawell,Luke McAlary,Jeremy S. Lum,Christen G. Chisholm,Sadaf T. Warraich,Ian P. Blair,Kara L. Vine,Darren N. Saunders,Justin J. Yerbury	2020	38
10	Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression Scientific Reports ·Ingrid Tarr,Emily P. McCann,Beben Benyamin,Timothy J. Peters,Natalie A. Twine,Katharine Y. Zhang,Qiongyi Zhao,Zong Hong Zhang,Dominic B. Rowe,Garth A. Nicholson,Denis C. Bauer,Susan J. Clark,Ian P. Blair,Kelly L. Williams	2019	30
11	Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress Cellular and Molecular Life Sciences ·Mark A. Halloran,Audrey Ragagnin,Marta Vidal,Sonam Parakh,Shu Yang,Benjamin Heng,Natalie Grima,Hamideh Shahheydari,Kai-Ying Soo,Ian P. Blair,Gilles J. Guillemin,Vinod Sundaramoorthy,Julie D. Atkin	2019	28
12	Motor Neuron Abnormalities Correlate with Impaired Movement in Zebrafish that Express Mutant Superoxide Dismutase 1 Zebrafish ·Katherine J. Robinson,Kristy C. Yuan,Emily K. Don,Alison Hogan,Claire Winnick,Madelaine C. Tym,Caitlin Lucas,Hamideh Shahheydari,Maxinne Watchon,Ian P. Blair,Julie D. Atkin,Garth A. Nicholson,Nicholas J. Cole,Angela S. Laird	2018	16
13	TDP-43 mutations causing amyotrophic lateral sclerosis are associated with altered expression of RNA-binding protein hnRNP K and affect the Nrf2 antioxidant pathway Human Molecular Genetics ·Diane Moujalled,Alexandra Grubman,Karla Acevedo,Shu Yang,Yazi D. Ke,Donia M. Moujalled,Clare Duncan,Aphrodite Caragounis,Nirma D. Perera,Bradley J. Turner,Mercedes Prudencio,Leonard Petrucelli,Ian P. Blair,Lars M. Ittner,Peter J. Crouch,Jeffrey R. Liddell,Anthony R. White	2017	62
14	ALS-associated mutant FUS inhibits macroautophagy which is restored by overexpression of Rab1 Cell Death Discovery ·K Y Soo,Jessica M. Sultana,Anna E. King,Rachel A.K. Atkinson,S T Warraich,Vinod Sundaramoorthy,Ian P. Blair,M A Farg,Julie D. Atkin	2015	52
15	A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindred Journal of Neurology Neurosurgery & Psychiatry ·Kelly L. Williams,Jennifer C. Durnall,Annora Thoeng,Sadaf T. Warraich,Garth A. Nicholson,Ian P. Blair	2009	26
16	TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosisbreakdown → Science ·Jemeen Sreedharan,Ian P. Blair,Vineeta B. Tripathi,Xun Hu,Caroline Vance,Boris Rogelj,Steven Ackerley,Jennifer C. Durnall,Kelly L. Williams,Emanuele Buratti,Francisco E. Baralle,Jacqueline de Belleroche,John D. Mitchell,P. Nigel Leigh,Ammar Al‐Chalabi,Christopher C.J. Miller,Garth A. Nicholson,Christopher E. Shaw	2008	2037
17	Identification, characterization, and association analysis of novel genes from the bipolar disorder susceptibility locus on chromosome 4q35 Psychiatric Genetics ·Ian P. Blair,Renee F. Badenhop,Anna Scimone,M. J. Moses,Jennifer A. Donald,Philip B. Mitchell,Peter R. Schofield	2005	2
18	Hereditary Sensory Neuropathy Type I: Haplotype Analysis Shows Founders in Southern England and Europe The American Journal of Human Genetics ·Garth A. Nicholson,Jennifer L. Dawkins,Ian P. Blair,Michaela Auer‐Grumbach,Sonal Brahmbhatt,D J Hulme	2001	21
19	A YAC-Based Transcript Map of Human Chromosome 9q22.1–q22.3 Encompassing the Loci for Hereditary Sensory Neuropathy Type I and Multiple Self-Healing Squamous Epithelioma Genomics ·Ian P. Blair,D J Hulme,Jennifer L. Dawkins,Garth A. Nicholson	1998	17
20	Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1→q22.3: exclusion of GAS1 and XPA Cytogenetic and Genome Research ·Ian P. Blair,Jennifer L. Dawkins,Garth A. Nicholson	1997	14

About Ian P. Blair

Ian P. Blair is a scholar working on Neurology, Genetics and Neurology, having authored 97 papers that have together received 6.0k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (66 papers), Neurogenetic and Muscular Disorders Research (44 papers), Neurological diseases and metabolism (20 papers), Parkinson's Disease Mechanisms and Treatments (20 papers), Hereditary Neurological Disorders (11 papers), Genetic Neurodegenerative Diseases (10 papers), Prion Diseases and Protein Misfolding (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Neurology (3.9k citations), Genetics (2.2k citations) and Neurology (1.1k citations). Ian P. Blair has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Garth A. Nicholson, Kelly L. Williams, Jennifer C. Durnall, Sadaf T. Warraich, Christopher E. Shaw, Caroline Vance, Shu Yang, P. Nigel Leigh, Xun Hu and Ammar Al‐Chalabi. Their work appears in journals such as Science, Nature Genetics and Nature Neuroscience.

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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