Karine Lascelles

3.0k total citations
25 papers, 858 citations indexed

About

Karine Lascelles is a scholar working on Neurology, Molecular Biology and Epidemiology. According to data from OpenAlex, Karine Lascelles has authored 25 papers receiving a total of 858 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 6 papers in Molecular Biology and 6 papers in Epidemiology. Recurrent topics in Karine Lascelles's work include Meningioma and schwannoma management (5 papers), Neurofibromatosis and Schwannoma Cases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Karine Lascelles is often cited by papers focused on Meningioma and schwannoma management (5 papers), Neurofibromatosis and Schwannoma Cases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Karine Lascelles collaborates with scholars based in United Kingdom, France and United States. Karine Lascelles's co-authors include Nadia Bahi‐Buisson, Nathalie Boddaert, Jamel Chelly, Chérif Beldjord, Karine Poirier, Caroline Elie, Tom Wong, Julian W.E. Jarman, Jonathan R. Clague and Vias Markides and has published in prestigious journals such as Brain, European Heart Journal and The American Journal of Human Genetics.

In The Last Decade

Karine Lascelles

25 papers receiving 843 citations

Peers

Countries citing papers authored by Karine Lascelles

Since Specialization

Citations

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

Fields of papers citing papers by Karine Lascelles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karine Lascelles

This figure shows the co-authorship network connecting the top 25 collaborators of Karine Lascelles. A scholar is included among the top collaborators of Karine Lascelles 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 Karine Lascelles. Karine Lascelles 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	Location, symptoms, and management of plexiform neurofibromas in 127 children with neurofibromatosis 1, attending the National Complex Neurofibromatosis 1 service, 2018–2019 2022 ·American Journal of Medical Genetics Part A ·(unknown), Rosalie E. Ferner, Grace Vassallo, (unknown), (unknown), (unknown), Darren Hargrave, (unknown), (unknown), (unknown), (unknown), (unknown), Karine Lascelles	6
2	A recent surge of fulminant and early onset subacute sclerosing panencephalitis (SSPE) in the United Kingdom: An emergence in a time of measles 2021 ·European Journal of Paediatric Neurology ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Anne-Marie Childs, (unknown), Frances Gibbon, Gareth M. Thomas, Jaspal Singh, Prab Prabhakar, Margaret Kaminska, Karine Lascelles, Yael Hacohen, Kevin Brown, Ming Lim	15
3	Trends in phenotype in the English paediatric neurofibromatosis type 2 cohort stratified by genetic severity 2019 ·Clinical Genetics ·Dorothy Halliday, (unknown), Grace Vassallo, Karine Lascelles, James C. Nicholson, (unknown), Geetha Anand, Martin Wasik, Pieter Pretorius, D. Gareth Evans, Allyson Parry	15
4	Early predictors of epilepsy and subsequent relapse in children with acute disseminated encephalomyelitis 2019 ·Multiple Sclerosis Journal ·Thomas Rossor, (unknown), Sukhvir Wright, Sophie Duignan, Karine Lascelles, Robert Robinson, Krishna B. Das, Olga Ciccarelli, Evangeline Wassmer, Cheryl Hemingway, Ming Lim, Yael Hacohen	38
5	Cerebral vasculopathy in childhood neurofibromatosis type 2: cause for concern? 2018 ·Developmental Medicine & Child Neurology ·Karine Lascelles, Shazia Afridi, Ata Siddiqui, Cheryl Hemingway, Rosalie E. Ferner, Vijeya Ganesan	6
6	Diagnosis of sporadic neurofibromatosis type 2 in the paediatric population 2018 ·Archives of Disease in Childhood ·Geetha Anand, (unknown), (unknown), (unknown), Michael Pike, (unknown), Sanjay R. Mehta, Allyson Parry, (unknown), James C. Nicholson, Karine Lascelles, (unknown), Frances Gibbon, (unknown), John Elston, D. Gareth Evans, Dorothy Halliday	17
7	Further refinement of COL4A1 and COL4A2 related cortical malformations 2018 ·European Journal of Medical Genetics ·Mara Cavallin, Manuèle Miné, (unknown), Nathalie Boddaert, (unknown), Thibault Coste, (unknown), (unknown), María Juliana Ballesta‐Martínez, Ganaëlle Remérand, Laurent Pasquier, (unknown), (unknown), Karine Lascelles, (unknown), Manoëlle Kossorotoff, Elisabeth Tournier‐Lasserve, Nadia Bahi‐Buisson	23
8	Clinical presentation and prognostic indicators in 100 adults and children with neurofibromatosis 1 associated non-optic pathway brain gliomas 2017 ·Journal of Neuro-Oncology ·Susan Byrne, Steve Connor, Karine Lascelles, Ata Siddiqui, Darren Hargrave, Rosalie E. Ferner	26
9	Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy 2016 ·The American Journal of Human Genetics ·Niklas Darín, Emma Reid, Laurence Prunetti, Lena Samuelsson, Ralf A. Husain, Matthew P. Wilson, Basma Yacoubi, Emma Footitt, W.K. Chong, Louise C. Wilson, Helen Prunty, Simon Pope, Simon Heales, Karine Lascelles, Mike Champion, Evangeline Wassmer, Pierangelo Veggiotti, Valérie de Crécy‐Lagard, Philippa B. Mills, Peter T. Clayton	106
10	Early-onset movement disorder and epileptic encephalopathy due to de novo dominant SCN8A mutation 2015 ·Seizure ·Rahul Singh, (unknown), Sushma Goyal, Heinz Jungbluth, Karine Lascelles	23
11	The wide spectrum of tubulinopathies: what are the key features for the diagnosis? 2014 ·Brain ·Nadia Bahi‐Buisson, Karine Poirier, Franck J. Fourniol, Yoann Saillour, Stéphanie Valence, Nicolas Lebrun, Marie Hully, (unknown), Nathalie Boddaert, Caroline Elie, Karine Lascelles, Isabelle Souville, Chérif Beldjord, Jamel Chelly	190
12	Atypical Presentation of Neuropsychiatric Lupus With Acanthosis Nigricans 2012 ·Pediatric Neurology ·J. Miquel, S. Hadj‐Rabia, Nathalie Boddaert, Karine Lascelles, Nadia Bahi‐Buisson	3
13	Clinical experience of entirely subcutaneous implantable cardioverter-defibrillators in children and adults: cause for caution 2012 ·European Heart Journal ·Julian W.E. Jarman, Karine Lascelles, Tom Wong, Vias Markides, Jonathan R. Clague, Janice Till	110
14	Neurodevelopmental movement disorders - an update on childhood motor stereotypies 2011 ·Developmental Medicine & Child Neurology ·Sinead Barry, Gillian Baird, Karine Lascelles, Penny Bunton, Tammy Hedderly	47
15	Encephalopathy andSCN1Amutations 2011 ·Epilepsia ·Shan Tang, Jean‐Pierre Lin, Elaine Hughes, Ata Siddiqui, Ming Lim, Karine Lascelles	15
16	GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex 2010 ·Brain ·Nadia Bahi‐Buisson, Karine Poirier, Nathalie Boddaert, Catherine Fallet‐Bianco, Nicola Specchio, Enrico Bertini, Ahmet Okay Çağlayan, Karine Lascelles, Caroline Elie, Jérôme Rambaud, Michel Baulac, Isabelle An, Patrícia Dias, Vincent des Portes, Marie Laure Moutard, Christine Soufflet, (unknown), Chérif Beldjord, Laurent Villard, Jamel Chelly	102
17	Combination of infantile spasms, non-epileptic seizures and complex movement disorder: A new case of ARX-related epilepsy 2008 ·Epilepsy Research ·Karine Poirier, Monika Eisermann, (unknown), Anna Kamińska, (unknown), Nathalie Boddaert, Yoann Saillour, Olivier Dulac, Isabelle Souville, Chérif Beldjord, Karine Lascelles, Perrine Plouin, Jamel Chelly, Nadia Bahi‐Buisson	26
18	Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase 2008 ·Seizure ·Nadia Bahi‐Buisson, Sandra Sabbagh, Christine Soufflet, Fabienne Escande, Nathalie Boddaert, Vassili Valayannopoulos, Christine Bellané‐Chantelot, Karine Lascelles, Olivier Dulac, Perrine Plouin, Pascale de Lonlay	36
19	Rasmussen's encephalitis followed by lupus erythematosus 2002 ·Developmental Medicine & Child Neurology ·Karine Lascelles, (unknown), Richard O. Robinson	7
20	Rasmussen's encephalitis followed by lupus erythematosus 2002 ·Developmental Medicine & Child Neurology ·Karine Lascelles, (unknown), Richard O. Robinson	5

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