Phillipa J. Lamont

4.2k citations

61 papers · 1.3k indexed · h-index 19

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 5%
Cardiology and Cardiovascular Medicine top 5%
Clinical Biochemistry top 2%
Genetics top 5%

Co-authors: Nigel G. Laing Mark R. Davis Gianina Ravenscroft Isabelle Nelson Douglass M. Turnbull Robert W. Taylor Frank Mastaglia Nicholas Wood
Topics: Muscle Physiology and Disorders (21 papers)Cardiomyopathy and Myosin Studies (19 papers)Mitochondrial Function and Pathology (11 papers)
Cited by: Clinical Biochemistry Cellular and Molecular Neuroscience Genetics
Journals: Brain Neurology PEDIATRICS
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 of co-authors of Phillipa J. Lamont

This figure shows the co-authorship network connecting the top 25 collaborators of Phillipa J. Lamont. A scholar is included among the top collaborators of Phillipa J. Lamont 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 Phillipa J. Lamont. Phillipa J. Lamont 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	Two Novel Variants in PI4KA in a Family Presenting With Hereditary Spastic Paraparesis 2024 ·Neurology Genetics ·J. Parmar,Elyshia McNamara,Phillipa J. Lamont,Kishore R. Kumar,(unknown),(unknown),Pak Leng Cheong,Gianina Ravenscroft	3
2	Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patients 2023 ·Brain Communications ·(unknown),Elisabetta Indelicato,David Pellerin,(unknown),Matt C. Danzi,Marie‐Josée Dicaire,Céline Bonnet,Henry Houlden,Stephan Züchner,Matthis Synofzik,Phillipa J. Lamont,M. Renaud,Sylvia Boesch,Bernard Brais	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 2023 ·Frontiers in Immunology ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Phillipa J. Lamont,Abha Chopra,Frank Mastaglia,Merrilee Needham,Jérôme D. Coudert	7
4	Partial loss‐of‐function variant in neuregulin 1 identified in family with heritable peripheral neuropathy 2022 ·Human Mutation ·(unknown),Ana M. Meireles,(unknown),Elyshia McNamara,Nigel G. Laing,Phillipa J. Lamont,Gianina Ravenscroft,William S. Talbot	5
5	The Impact of Next-Generation Sequencing on the Diagnosis, Treatment, and Prevention of Hereditary Neuromuscular Disorders 2020 ·Molecular Diagnosis & Therapy ·Sarah J. Beecroft,Phillipa J. Lamont,Samantha Edwards,Hayley Goullée,Mark R. Davis,Nigel G. Laing,Gianina Ravenscroft	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 2020 ·BMJ Open ·Sarah Milne,Louise A. Corben,Melissa Roberts,David J. Szmulewicz,Joshua Burns,Anneke Grobler,(unknown),(unknown),Christina Liang,Phillipa J. Lamont,(unknown),(unknown),Carolyn M. Sue,Kim Dalziel,(unknown),(unknown),(unknown),(unknown),Martin B. Delatycki	13
7	Altered myogenesis and premature senescence underlie human TRIM32-related myopathy 2019 ·Acta Neuropathologica Communications ·Emilia Servián‐Morilla,Macarena Cabrera‐Serrano,Eloy Rivas,Alejandra Carvajal,Phillipa J. Lamont,Ana L. Pelayo‐Negro,Gianina Ravenscroft,Reimar Junckerstorff,(unknown),Sue Fletcher,A.M. Adams,Fabiola Mavillard,(unknown),José Luis Nieto-González,Nigel G. Laing,Carmen Paradas	20
8	STRetch: detecting and discovering pathogenic short tandem repeat expansions 2018 ·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	82
9	Cystinosis distal myopathy, novel clinical, pathological and genetic features 2017 ·Neuromuscular Disorders ·Macarena Cabrera‐Serrano,Reimar Junckerstorff,(unknown),Alan Pestronk,Nigel G. Laing,Conrad C. Weihl,Phillipa J. Lamont	7
10	New era in genetics of early-onset muscle disease: Breakthroughs and challenges 2016 ·Seminars in Cell and Developmental Biology ·Gianina Ravenscroft,Mark R. Davis,Phillipa J. Lamont,Alistair R. R. Forrest,Nigel G. Laing	18
11	A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome 2015 ·Mitochondrion ·Rachael M. Duff,Anne-Marie J. Shearwood,Judith A. Ermer,(unknown),Rebecca Gooding,Tara R. Richman,Shanti Balasubramaniam,David R. Thorburn,Oliver Rackham,Phillipa J. Lamont,Aleksandra Filipovska	9
12	Clinical utility gene card for: Nemaline myopathy – update 2015 2015 ·European Journal of Human Genetics ·Kristen L. Nowak,Mark R. Davis,Carina Wallgren‐Pettersson,Phillipa J. Lamont,Nigel G. Laing	10
13	Novel CHKB mutation expands the megaconial muscular dystrophy phenotype 2014 ·Muscle & Nerve ·Macarena Cabrera‐Serrano,Reimar Junckerstorff,(unknown),Padma Sivadorai,Richard J. N. Allcock,Phillipa J. Lamont,Nigel G. Laing	15
14	Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity 2008 ·Annals of Neurology ·Rishika A. Pace,Rachel A. Peat,Naomi L. Baker,Laura Zamurs,Matthias Mörgelin,Melita Irving,(unknown),John F. Bateman,David Mowat,Nicholas Smith,Phillipa J. Lamont,Steven A. Moore,Katherine D. Mathews,Kathryn N. North,Shireen R. Lamandé	54
15	Quality of life in Friedreich ataxia: what clinical, social and demographic factors are important? 2007 ·European Journal of Neurology ·Carmen L. Wilson,Michael Fahey,Louise A. Corben,V. R. Collins,Andrew Churchyard,Phillipa J. Lamont,M. B. Delatycki	41
16	Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive 2004 ·Neuropediatrics ·Phillipa J. Lamont,David R. Thorburn,Vicki Fabian,Jiri Vajsar,Cynthia Hawkins,Ann Saada,Hayley J. Durling,Nigel G. Laing,Yoram Nevo	17
17	Fifty year follow-up of a patient with central core disease shows slow but definite progression 1998 ·Neuromuscular Disorders ·Phillipa J. Lamont,Victor Dubowitz,D. N. Landon,Martin B. Davis,J A Morgan-Hughes	20
18	Pearson's syndrome without marrow involvement 1997 ·Archives of Disease in Childhood ·A. A. M. Morris,Phillipa J. Lamont,Peter T. Clayton	11
19	Differences in Diaphragm Fiber Types in SIDS Infants 1995 ·Journal of Neuropathology & Experimental Neurology ·Phillipa J. Lamont,(unknown),John Hilton,Roger Pamphlett	8
20	Recurrent lymphomatoid granulomatosis and isolated CNS involvement 1995 ·Journal of Clinical Neuroscience ·Lali H.S. Sekhon,Michael K. Morgan,Elizabeth Salisbury,(unknown),Phillipa J. Lamont	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) and Mitochondrial Function and Pathology (11 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.

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