Phillipa J. Lamont

4.2k citations

61 papers · 1.3k indexed · h-index 19

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 6
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 11
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 11
- Genomics and Rare Diseases 7
Cardiology and Cardiovascular Medicine top 5%
- Cardiomyopathy and Myosin Studies 19
Molecular Biology top 10%
- Muscle Physiology and Disorders 21
- Mitochondrial Function and Pathology 11
- Nuclear Structure and Function 5

Co-authors: Nigel G. Laing Mark R. Davis Gianina Ravenscroft Isabelle Nelson Douglass M. Turnbull Robert W. Taylor Frank Mastaglia Nicholas Wood
Cited by: Clinical Biochemistry Cellular and Molecular Neuroscience Genetics
Journals: Brain (3 papers)Neurology (1 paper)PEDIATRICS (1 paper)
Partner nations: Australia United States United Kingdom

In The Last Decade

Phillipa J. Lamont

58 papers receiving 1.3k citations

Peers

Countries citing papers authored by Phillipa J. Lamont

Since Specialization

Citations

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

Fields of papers citing papers by Phillipa J. Lamont

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Phillipa J. Lamont. 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 Phillipa J. Lamont. The network helps show where Phillipa J. Lamont may publish in the future.

Co-authorship network

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Two Novel Variants in PI4KA in a Family Presenting With Hereditary Spastic Paraparesis Neurology Genetics ·J. Parmar,Elyshia McNamara,Phillipa J. Lamont,Kishore R. Kumar,Audrey Rick,Marion Stoll,Pak Leng Cheong,Gianina Ravenscroft	2024	3
2	Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patients Brain Communications ·Catherine Ashton,Elisabetta Indelicato,David Pellerin,Guillemette Clément,Matt C. Danzi,Marie‐Josée Dicaire,Céline Bonnet,Henry Houlden,Stephan Züchner,Matthis Synofzik,Phillipa J. Lamont,M. Renaud,Sylvia Boesch,Bernard Brais	2023	12
3	Uncovering the significance of expanded CD8+ large granular lymphocytes in inclusion body myositis: Insights into T cell phenotype and functional alterations, and disease severity Frontiers in Immunology ·Emily McLeish,Anuradha Sooda,Nataliya Slater,Barbara Kachigunda,Kelly Beer,Shereen Paramalingam,Phillipa J. Lamont,Abha Chopra,Frank Mastaglia,Merrilee Needham,Jérôme D. Coudert	2023	7
4	Partial loss‐of‐function variant in neuregulin 1 identified in family with heritable peripheral neuropathy Human Mutation ·Daniel E. Lysko,Ana M. Meireles,Chiara Folland,Elyshia McNamara,Nigel G. Laing,Phillipa J. Lamont,Gianina Ravenscroft,William S. Talbot	2022	5
5	The Impact of Next-Generation Sequencing on the Diagnosis, Treatment, and Prevention of Hereditary Neuromuscular Disorders Molecular Diagnosis & Therapy ·Sarah J. Beecroft,Phillipa J. Lamont,Samantha Edwards,Hayley Goullée,Mark R. Davis,Nigel G. Laing,Gianina Ravenscroft	2020	7
6	Rehabilitation for ataxia study: protocol for a randomised controlled trial of an outpatient and supported home-based physiotherapy programme for people with hereditary cerebellar ataxia BMJ Open ·Sarah Milne,Louise A. Corben,Melissa Roberts,David J. Szmulewicz,Joshua Burns,Anneke Grobler,Shannon Williams,Jillian Chua,Christina Liang,Phillipa J. Lamont,Alison C Grootendorst,Libby Massey,Carolyn M. Sue,Kim Dalziel,Desireé LaGrappe,Liz Willis,Aleka Freijah,Paul Gerken,Martin B. Delatycki	2020	13
7	Altered myogenesis and premature senescence underlie human TRIM32-related myopathy Acta Neuropathologica Communications ·Emilia Servián‐Morilla,Macarena Cabrera‐Serrano,Eloy Rivas,Alejandra Carvajal,Phillipa J. Lamont,Ana L. Pelayo‐Negro,Gianina Ravenscroft,Reimar Junckerstorff,Jason Dyke,Sue Fletcher,A.M. Adams,Fabiola Mavillard,M. Fernández-García,José Luis Nieto-González,Nigel G. Laing,Carmen Paradas	2019	20
8	STRetch: detecting and discovering pathogenic short tandem repeat expansions Genome biology ·Harriet Dashnow,Monkol Lek,Belinda Phipson,Andreas Halman,Simon Sadedin,Andrew Lonsdale,Mark R. Davis,Phillipa J. Lamont,Joshua S. Clayton,Nigel G. Laing,Daniel G. MacArthur,Alicia Oshlack	2018	82
9	Cystinosis distal myopathy, novel clinical, pathological and genetic features Neuromuscular Disorders ·Macarena Cabrera‐Serrano,Reimar Junckerstorff,Ali Alisheri,Alan Pestronk,Nigel G. Laing,Conrad C. Weihl,Phillipa J. Lamont	2017	7
10	New era in genetics of early-onset muscle disease: Breakthroughs and challenges Seminars in Cell and Developmental Biology ·Gianina Ravenscroft,Mark R. Davis,Phillipa J. Lamont,Alistair R. R. Forrest,Nigel G. Laing	2016	18
11	A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome Mitochondrion ·Rachael M. Duff,Anne-Marie J. Shearwood,Judith A. Ermer,Giulia Rossetti,Rebecca Gooding,Tara R. Richman,Shanti Balasubramaniam,David R. Thorburn,Oliver Rackham,Phillipa J. Lamont,Aleksandra Filipovska	2015	9
12	Clinical utility gene card for: Nemaline myopathy – update 2015 European Journal of Human Genetics ·Kristen L. Nowak,Mark R. Davis,Carina Wallgren‐Pettersson,Phillipa J. Lamont,Nigel G. Laing	2015	10
13	Novel CHKB mutation expands the megaconial muscular dystrophy phenotype Muscle & Nerve ·Macarena Cabrera‐Serrano,Reimar Junckerstorff,Vanessa Atkinson,Padma Sivadorai,Richard J. N. Allcock,Phillipa J. Lamont,Nigel G. Laing	2014	15
14	Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity Annals of Neurology ·Rishika A. Pace,Rachel A. Peat,Naomi L. Baker,Laura Zamurs,Matthias Mörgelin,Melita Irving,Naomi E. Adams,John F. Bateman,David Mowat,Nicholas Smith,Phillipa J. Lamont,Steven A. Moore,Katherine D. Mathews,Kathryn N. North,Shireen R. Lamandé	2008	54
15	Quality of life in Friedreich ataxia: what clinical, social and demographic factors are important? European Journal of Neurology ·Carmen L. Wilson,Michael Fahey,Louise A. Corben,V. R. Collins,Andrew Churchyard,Phillipa J. Lamont,M. B. Delatycki	2007	41
16	Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive Neuropediatrics ·Phillipa J. Lamont,David R. Thorburn,Vicki Fabian,Jiri Vajsar,Cynthia Hawkins,Ann Saada,Hayley J. Durling,Nigel G. Laing,Yoram Nevo	2004	17
17	Fifty year follow-up of a patient with central core disease shows slow but definite progression Neuromuscular Disorders ·Phillipa J. Lamont,Victor Dubowitz,D. N. Landon,Martin B. Davis,J A Morgan-Hughes	1998	20
18	Pearson's syndrome without marrow involvement Archives of Disease in Childhood ·A. A. M. Morris,Phillipa J. Lamont,Peter T. Clayton	1997	11
19	Differences in Diaphragm Fiber Types in SIDS Infants Journal of Neuropathology & Experimental Neurology ·Phillipa J. Lamont,CHRISTOPHER CHOW,John Hilton,Roger Pamphlett	1995	8
20	Recurrent lymphomatoid granulomatosis and isolated CNS involvement Journal of Clinical Neuroscience ·Lali H.S. Sekhon,Michael K. Morgan,Elizabeth Salisbury,Julienne Grace,Phillipa J. Lamont	1995	3

About Phillipa J. Lamont

Phillipa J. Lamont is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Clinical Biochemistry, having authored 61 papers that have together received 1.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (21 papers), Cardiomyopathy and Myosin Studies (19 papers), Mitochondrial Function and Pathology (11 papers), Genetic Neurodegenerative Diseases (11 papers), Neurogenetic and Muscular Disorders Research (11 papers), Genomics and Rare Diseases (7 papers), Metabolism and Genetic Disorders (6 papers) and Nuclear Structure and Function (5 papers). The work is most often cited by research in Clinical Biochemistry (197 citations), Cellular and Molecular Neuroscience (366 citations) and Genetics (173 citations). Phillipa J. Lamont has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Nigel G. Laing, Mark R. Davis, Gianina Ravenscroft, Isabelle Nelson, Douglass M. Turnbull, Robert W. Taylor, Frank Mastaglia, Nicholas Wood, Macarena Cabrera‐Serrano and Vicki Fabian. Their work appears in journals such as Brain, Neurology and PEDIATRICS.

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.

Explore authors with similar magnitude of impact