Ian P. Blair

15.3k citations

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

Neurology top 0.1%
Molecular Biology top 2%
Genetics top 0.2%
Neurology top 0.5%
Cellular and Molecular Neuroscience top 2%

Co-authors: Garth A. Nicholson Kelly L. Williams Jennifer C. Durnall Sadaf T. Warraich Christopher E. Shaw Caroline Vance Shu Yang P. Nigel Leigh
Topics: Amyotrophic Lateral Sclerosis Research (66 papers)Neurogenetic and Muscular Disorders Research (44 papers)Neurological diseases and metabolism (20 papers)
Cited by: Neurology Genetics
Journals: Science Nature Genetics Nature Neuroscience
Partner nations: Australia United States United Kingdom

In The Last Decade

Ian P. Blair

93 papers receiving 5.9k 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.

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

2008 2.0k citations Jemeen Sreedharan, Ian P. Blair et al. Science profile →
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

2004 602 citations Ian P. Blair, Garth A. Nicholson et al. The American Journal of Human Genetics profile →
C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking

2014 377 citations Vinod Sundaramoorthy, Shu Yang et al. Human Molecular Genetics profile →

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 of co-authors of Ian P. Blair

This figure shows the co-authorship network connecting the top 25 collaborators of Ian P. Blair. A scholar is included among the top collaborators of Ian P. Blair 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 Ian P. Blair. Ian P. Blair 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	Multi-region brain transcriptomic analysis of amyotrophic lateral sclerosis reveals widespread RNA alterations and substantial cerebellum involvement 2025 ·Molecular Neurodegeneration ·Natalie Grima,(unknown),Claire E. Shepherd,Lyndal Henden,Thiri Zaw,Luke Carroll,Dominic B. Rowe,Matthew C. Kiernan,Ian P. Blair,Kelly L. Williams	0
2	C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD 2024 ·Molecular Neurobiology ·(unknown),Audrey Ragagnin,Sonam Parakh,(unknown),Kai Y. Soo,Marta Vidal,Cyril J. Jagaraj,(unknown),(unknown),Sina Shadfar,Emily K. Don,Anand K. Deva,Garth A. Nicholson,Dominic B. Rowe,Ian P. Blair,Shu Yang,Julie D. Atkin	4
3	Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry 2024 ·Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Lyndal Henden,Liam G. Fearnley,(unknown),(unknown),Dominic B. Rowe,Matthew C. Kiernan,Roger Pamphlett,Melanie Bahlo,Ian P. Blair,Kelly L. Williams	0
4	ALS-linked CCNF variant disrupts motor neuron ubiquitin homeostasis 2023 ·Human Molecular Genetics ·Natalie E. Farrawell,(unknown),Luke McAlary,(unknown),(unknown),Dzung Do‐Ha,Stephanie L. Rayner,Ian P. Blair,Roger S. Chung,Justin J. Yerbury,Lezanne Ooi,Darren N. Saunders	4
5	Characterising the Genetic Landscape of Amyotrophic Lateral Sclerosis: A Catalogue and Assessment of Over 1,000 Published Genetic Variants 2023 ·Journal of Neuromuscular Diseases ·Emily P. McCann,Natalie Grima,Jennifer A. Fifita,(unknown),Klaus Lehnert,Lyndal Henden,Ian P. Blair,Kelly L. Williams	4
6	Association between DNA methylation variability and self-reported exposure to heavy metals 2022 ·Scientific Reports ·(unknown),Marta F. Nabais,Tian Lin,Kelly L. Williams,Leanne Wallace,Anjali K. Henders,Ian P. Blair,Naomi R. Wray,Roger Pamphlett,Allan F. McRae	10
7	NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk 2022 ·Neurobiology of Aging ·Natalie Grima,Lyndal Henden,Liam G. Fearnley,Dominic B. Rowe,(unknown),Roger Pamphlett,(unknown),Matthew C. Kiernan,(unknown),Hannah C. Timmins,Margaret Zoing,Melanie Bahlo,Ian P. Blair,Kelly L. Williams	0
8	Sensitive Detection of Motor Neuron Disease Derived Exosomal miRNA Using Electrocatalytic Activity of Gold‐Loaded Superparamagnetic Ferric Oxide Nanocubes 2020 ·ChemElectroChem ·Mostafa Kamal Masud,Rabbee G. Mahmudunnabi,(unknown),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	20
9	Ubiquitin Homeostasis Is Disrupted in TDP-43 and FUS Cell Models of ALS 2020 ·iScience ·Natalie E. Farrawell,Luke McAlary,Jeremy S. Lum,(unknown),Sadaf T. Warraich,Ian P. Blair,Kara L. Vine,Darren N. Saunders,Justin J. Yerbury	38
10	Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression 2019 ·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	30
11	Amyotrophic lateral sclerosis-linked UBQLN2 mutants inhibit endoplasmic reticulum to Golgi transport, leading to Golgi fragmentation and ER stress 2019 ·Cellular and Molecular Life Sciences ·Mark A. Halloran,Audrey Ragagnin,Marta Vidal,Sonam Parakh,Shu Yang,Benjamin Heng,Natalie Grima,Hamideh Shahheydari,(unknown),Ian P. Blair,Gilles J. Guillemin,Vinod Sundaramoorthy,Julie D. Atkin	28
12	Motor Neuron Abnormalities Correlate with Impaired Movement in Zebrafish that Express Mutant Superoxide Dismutase 1 2018 ·Zebrafish ·Katherine J. Robinson,Kristy C. Yuan,Emily K. Don,Alison Hogan,Claire Winnick,(unknown),(unknown),Hamideh Shahheydari,Maxinne Watchon,Ian P. Blair,Julie D. Atkin,Garth A. Nicholson,Nicholas J. Cole,Angela S. Laird	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 2017 ·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	62
14	ALS-associated mutant FUS inhibits macroautophagy which is restored by overexpression of Rab1 2015 ·Cell Death Discovery ·(unknown),(unknown),Anna E. King,Rachel A.K. Atkinson,(unknown),Vinod Sundaramoorthy,Ian P. Blair,(unknown),Julie D. Atkin	52
15	A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindred 2009 ·Journal of Neurology Neurosurgery & Psychiatry ·Kelly L. Williams,Jennifer C. Durnall,Annora Thoeng,Sadaf T. Warraich,Garth A. Nicholson,Ian P. Blair	26
16	TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosisbreakdown → 2008 ·Science ·Jemeen Sreedharan,Ian P. Blair,(unknown),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	2037
17	Identification, characterization, and association analysis of novel genes from the bipolar disorder susceptibility locus on chromosome 4q35 2005 ·Psychiatric Genetics ·Ian P. Blair,Renee F. Badenhop,Anna Scimone,M. J. Moses,Jennifer A. Donald,Philip B. Mitchell,Peter R. Schofield	2
18	Hereditary Sensory Neuropathy Type I: Haplotype Analysis Shows Founders in Southern England and Europe 2001 ·The American Journal of Human Genetics ·Garth A. Nicholson,Jennifer L. Dawkins,Ian P. Blair,Michaela Auer‐Grumbach,Sonal Brahmbhatt,D J Hulme	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 1998 ·Genomics ·Ian P. Blair,D J Hulme,Jennifer L. Dawkins,Garth A. Nicholson	17
20	Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1→q22.3: exclusion of GAS1 and XPA 1997 ·Cytogenetic and Genome Research ·Ian P. Blair,Jennifer L. Dawkins,Garth A. Nicholson	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) and Neurological diseases and metabolism (20 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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