Julian Blake

2.3k citations

39 papers · 1.3k indexed · h-index 20

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders

Papers in

Cellular and Molecular Neuroscience 26
- Hereditary Neurological Disorders 23
- Genetic Neurodegenerative Diseases 15
Neurology 7
- Botulinum Toxin and Related Neurological Disorders 8
- Neurological diseases and metabolism 7
- Peripheral Neuropathies and Disorders 5

Co-authors: Mary M. Reilly Henry Houlden Matilde Laurá James M. Polke Alexander M. Rossor R. H. M. King Sinéad M. Murphy Jonathan M. Cooper
Journals: Neuromuscular Disorders (6 papers)Journal of the Peripheral Nervous System (5 papers)Journal of Neurology Neurosurgery & Psychiatry (5 papers)Brain (4 papers)Neurology (3 papers)
Partner nations: United Kingdom United States Italy

In The Last Decade

Julian Blake

38 papers receiving 1.3k citations

Peers

Countries citing papers authored by Julian Blake

Since Specialization

Citations

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

Fields of papers citing papers by Julian Blake

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julian Blake. 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 Julian Blake. The network helps show where Julian Blake may publish in the future.

Co-authors

The 25 scholars most cited alongside Julian Blake, 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 Julian Blake Line = papers co-authored together Julian Blake links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Intermediate conduction velocity in two cases of Charcot−Marie−Tooth disease type 1A European Journal of Neurology ·Pedro José Tomaselli, Julian Blake, James M. Polke, Osvaldo J. M. Nascimento, Mary M. Reilly, Wilson Marques, Matilde Laurá	2024	2
2	Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease Brain ·Christopher J. Record, Menelaos Pipis, Mariola Skorupinska, Julian Blake, Roy Poh, James M. Polke, A M El-Gatit, Tina Nanji, Stephan Züchner, Andrea Cortese, Henry Houlden, Alexander M. Rossor, Matilde Laurá, Mary M. Reilly	2024	13
3	Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1 Brain ·Menelaos Pipis, Kuldeep Singh, Roy Poh, Stéphanie Efthymiou, James M. Polke, Mariola Skorupinska, Julian Blake, Alexander M. Rossor, John J. Moran, Pinki Munot, Francesco Muntoni, Matilde Laurá, John Svaren, Mary M. Reilly	2023	3
4	Charcot-Marie-Tooth disease type 2CC due toNEFHvariants causes a progressive, non-length-dependent, motor-predominant phenotype Journal of Neurology Neurosurgery & Psychiatry ·Menelaos Pipis, Andrea Cortese, James M. Polke, Roy Poh, Jana Vandrovcová, Matilde Laurá, Mariola Skorupinska, Arnaud Jacquier, Raúl Juntas‐Morales, Philippe Latour, Philippe Petiot, Guilhem Solé, Yves Fromes, Sachit Shah, Julian Blake, Byung‐Ok Choi, Ki Wha Chung, Tanya Stojkovic, Alexander M. Rossor, Mary M. Reilly	2021	11
5	Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre Neuromuscular Disorders ·Enrico Bugiardini, Anne-Emmanuella Yeo, Rahul Phadke, David S. Lynch, Andrea Cortese, Lucy Feng, Qiang Gang, Alan Pittman, Jasper M. Morrow, Chris Turner, Aisling Carr, Rosaline C. M. Quinlivan, Alexander M. Rossor, Janice L. Holton, Matt Parton, Julian Blake, Mary M. Reilly, Henry Houlden, Emma Matthews, Michael G. Hanna	2019	10
6	IGHMBP2 mutation associated with organ-specific autonomic dysfunction Neuromuscular Disorders ·Pedro José Tomaselli, Alejandro Horga, Alexander M. Rossor, Zane Jaunmuktane, Andrea Cortese, Julian Blake, Bek Hyun Cho, Henry Houlden, Mary M. Reilly	2018	17
7	Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene Neuromuscular Disorders ·Alexander M. Rossor, Jasper M. Morrow, James M. Polke, Sinéad M. Murphy, Henry Houlden, Matilde Laurá, Hadi Manji, Julian Blake, Mary M. Reilly	2016	23
8	Novel HSAN1 Mutation in Serine Palmitoyltransferase Resides at a Putative Phosphorylation Site That Is Involved in Regulating Substrate Specificity NeuroMolecular Medicine ·Daniela Ernst, Sinéad M. Murphy, Mike Komnik, Wei Yu, Alaa Othman, Matilde Laurá, Yo‐Tsen Liu, Anke Penno, Julian Blake, Michael Donaghy, Henry Houlden, Mary M. Reilly, Thorsten Hornemann	2015	25
9	Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegia Brain ·Alejandro Horga, Robert D. S. Pitceathly, Julian Blake, Claudio Anderson, Pedro Zapater, Carl Fratter, Ese Mudanohwo, Gordon T. Plant, Henry Houlden, Mary G. Sweeney, Michael G. Hanna, Mary M. Reilly	2014	27
10	Rapidly progressive asymmetrical weakness in Charcot–Marie–Tooth disease type 4J resembles chronic inflammatory demyelinating polyneuropathy Neuromuscular Disorders ·Ellen Cottenie, Manoj P. Menezes, Alexander M. Rossor, Jasper M. Morrow, Tarek Yousry, D J Dick, Janice R. Anderson, Zane Jaunmuktane, Sebastian Brandner, Julian Blake, Henry Houlden, Mary M. Reilly	2013	34
11	Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing Journal of Neurology Neurosurgery & Psychiatry ·Sinéad M. Murphy, Matilde Laurá, Katherine A. Fawcett, Amelie Pandraud, Yo‐Tsen Liu, Gabrielle L. Davidson, Alexander M. Rossor, James M. Polke, Victoria Castleman, Hadi Manji, Michael P. Lunn, Jorg Matthys, Gita Ramdharry, Mary B. Davis, Julian Blake, Henry Houlden, Mary M. Reilly	2012	257
12	A novel p.Glu175X premature stop mutation in the C‐terminal end of HSP27 is a cause of CMT2 Journal of the Peripheral Nervous System ·Alexander M. Rossor, Gabrielle L. Davidson, Julian Blake, James M. Polke, Sinéad M. Murphy, Henry Houlden, Amy Innes, Bernadett Kalmár, Linda Greensmith, Mary M. Reilly	2012	14
13	Neuropathy in a Human Without the PMP22 Gene Archives of Neurology ·Mario Saporta, István Katona, Xuebao Zhang, Helen Roper, Matthew Karny, Fiona MacDonald, Louise Brueton, Julian Blake, Ueli Suter, Mary M. Reilly, Michael E. Shy, Jun Li	2011	20
14	Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a myelin protein zero p.Ile112Thr mutation Neuromuscular Disorders ·Sinéad M. Murphy, Matilde Laurá, Julian Blake, James M. Polke, Fion Bremner, Mary M. Reilly	2011	17
15	A novel mutation in the nerve‐specific 5′UTR of the GJB1 gene causes X‐linked Charcot‐Marie‐Tooth disease Journal of the Peripheral Nervous System ·Sinéad M. Murphy, James M. Polke, Hadi Manji, Julian Blake, Costa, João da, [entre 1660 e 1689], Mary G. Sweeney, Henry Houlden, Sebastian Brandner, Mary M. Reilly	2011	26
16	The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy Neuromuscular Disorders ·Henry Houlden, Matilde Laurá, Lionel Ginsberg, Heinz Jungbluth, S. Robb, Julian Blake, Susan W. Robinson, R. H. M. King, Mary M. Reilly	2009	76
17	GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology Genomics ·Sahar Al‐Mahdawi, Ricardo Mouro Pinto, Dhaval Varshney, Lorraine Lawrence, Margaret B. Lowrie, Siân Hughes, Zoë Webster, Julian Blake, Jonathan M. Cooper, R. H. M. King, Mark A. Pook	2006	179
18	Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I) Brain ·Henry Houlden, R. H. M. King, Julian Blake, Mike Groves, Seth Love, Cathy E. Woodward, Simon Hammans, James A. R. Nicoll, Graham Lennox, Dominic G. O’Donovan, Carolyn Gabriel, P K Thomas, Mary M. Reilly	2005	97
19	Mitochondrial DNA Depletion Syndrome is Expressed in Amniotic Fluid Cell Cultures American Journal Of Pathology ·Julian Blake, Jan‐Willem Taanman, R.T. D'Agnolo, R. G. F. Gray, Jonathan M. Cooper, Patrick McKiernan, James V. Leonard, Anthony H.V. Schapira	1999	32
20	Liver failure associated with mitochondrial DNA depletion Journal of Hepatology ·Andrew A. M. Morris, Jan‐Willem Taanman, Julian Blake, Jonathan M. Cooper, Brian Lake, M Malone, Seth Love, Peter T. Clayton, James V. Leonard, Anthony H.V. Schapira	1998	76

About Julian Blake

Julian Blake is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Clinical Biochemistry and Cell Biology, having authored 39 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (23 papers), Genetic Neurodegenerative Diseases (15 papers), Botulinum Toxin and Related Neurological Disorders (8 papers), Neurological diseases and metabolism (7 papers), Peripheral Neuropathies and Disorders (5 papers), Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (3 papers) and Cellular transport and secretion (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (921 citations), Neurology (259 citations), Neurology (357 citations), Clinical Biochemistry (116 citations) and Cell Biology (238 citations). Julian Blake has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Mary M. Reilly, Henry Houlden, Matilde Laurá, James M. Polke, Alexander M. Rossor, R. H. M. King, Sinéad M. Murphy, Jonathan M. Cooper, Hadi Manji and Michael P. Lunn. Their work appears in journals such as Neuromuscular Disorders, Journal of the Peripheral Nervous System, Journal of Neurology Neurosurgery & Psychiatry, Brain and Neurology.

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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