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S. Mordekar · SciRah

Researcher profile · Semantic Scholar

S. Mordekar

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S. Mordekar — researcher profile on SciRah

h-index: 22
Works: 95
Citations: 1,358

Most-cited papers

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.
M. Kurian, J. Zhen, Shu-Yuan Cheng, Yan Li +11 more
2009Journal of Clinical Investigation220 citations Open access
Semantic Scholar
Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
M. Kurian, Yan Li, J. Zhen, E. Meyer +18 more
2010Lancet Neurology193 citations Open access
Semantic Scholar
Role of imaging in the diagnosis of acute bacterial meningitis and its complications
D. Hughes, Ashok Raghavan, S. Mordekar, P. D. Griffiths +1 more
2010Postgraduate medical journal99 citations
Semantic Scholar
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defect
Kyle A Metz, Xin-Chen Teng, I. Coppens, Heather M. Lamb +39 more
2018Annals of Neurology59 citations Open access
Semantic Scholar
Pharmacological management of abnormal tone and movement in cerebral palsy
D. Lumsden, B. Crowe, A. Basu, S. Amin +8 more
2019Archives of Disease in Childhood49 citations Open access
Semantic Scholar
Paediatric post-septal and pre-septal cellulitis: 10 years' experience at a tertiary-level children's hospital.
Anu Mathew, E. Craig, R. Al-Mahmoud, R. Batty +4 more
2014British Journal of Radiology46 citations Open access
Semantic Scholar
An investigation into the relationship between vigabatrin, movement disorders, and brain magnetic resonance imaging abnormalities in children with infantile spasms
C. Y. Fong, J. Osborne, S. Edwards, C. Hemingway +16 more
2013Developmental Medicine & Child Neurology40 citations
Semantic Scholar
Encephalopathy in children: an approach to assessment and management
E. Davies, D. Connolly, S. Mordekar
2011Archives of Disease in Childhood38 citations
Semantic Scholar
Retention rate of levetiracetam in children with intractable epilepsy at 1 year.
D. Peake, S. Mordekar, J. Gosalakkal, B. Mukhtyar +7 more
2007Seizure38 citations Open access
Semantic Scholar
The Phenotypic Continuum of ATP1A3-Related Disorders
Aikaterini Vezyroglou, Rhoda Akilapa, K. Barwick, S. Koene +25 more
2022Neurology36 citations Open access
Semantic Scholar
False diagnosis of papilloedema and idiopathic intracranial hypertension.
A. Mishra, S. Mordekar, I. Rennie, P. Baxter
2007European journal of paediatric neurology33 citations
Semantic Scholar
The Phenotypic Continuum of ATPLA3-Related Disorders.
Aikaterini Vezyroglou, Rhoda Akilapa, K. Barwick, S. Koene +25 more
2022Neurology32 citations Open access
Semantic Scholar
Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome.
S. Masnada, C. Sarret, C. Antonello, A. Fadilah +16 more
2021Molecular Genetics and Metabolism29 citations
Semantic Scholar
Nonketotic hyperglycinemia case series
M. Iqbal, M. Prasad, S. Mordekar
2015Journal of Pediatric Neurosciences29 citations Open access
Semantic Scholar
The value of long term EEG monitoring in children: a comparison of ambulatory EEG and video telemetry.
J. J. Alix, R. Kandler, S. Mordekar
2014Seizure27 citations Open access
Semantic Scholar
Movement disorders associated with complex regional pain syndrome in children
S. Agrawal, Christopher D. Rittey, N. Harrower, J. Goddard +1 more
2009Developmental Medicine & Child Neurology27 citations Open access
Semantic Scholar
The use of MR imaging and spectroscopy of the brain in children investigated for developmental delay: What is the most appropriate imaging strategy?
P. Griffiths, R. Batty, D. Warren, A. Hart +4 more
2011European Radiology25 citations
Semantic Scholar
Skull base osteomyelitis leading to lateral medullary syndrome in a child.
J. Ng, D. Connolly, C. Rittey, S. Mordekar
2007European journal of paediatric neurology25 citations
Semantic Scholar
Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms
Kelsey A. Nolden, John M. Egner, J. Collier, O. Russell +20 more
2022Life Science Alliance23 citations Open access
Semantic Scholar
Fifteen minute consultation: tics and Tourette syndrome
Tsui-Ong Min, S. Mordekar, A. Seal
2015Archives of Disease in Childhood - Education and Practice23 citations Open access
Semantic Scholar
Clinical report: AN INTERSTITIAL deletion of 16p13.11 detected by array CGH in a patient with infantile spasms.
M. Balasubramanian, Kath Smith, S. Mordekar, MJ Parker
2011European Journal of Medical Genetics22 citations
Semantic Scholar
Corticosteroid treatment of behaviour, language and motor regression in childhood disintegrative disorder.
S. Mordekar, M. Prendergast, A. Chattopadhyay, P. Baxter
2009European journal of paediatric neurology22 citations
Semantic Scholar
Profound encephalopathy with complete recovery in three children with familial hemiplegic migraine
A. Hart, R. Trinick, D. Connolly, S. Mordekar
2009Journal of Paediatrics and Child Health20 citations
Semantic Scholar
Intracranial calcification in early infantile Krabbe disease: nothing new under the sun
J. Livingston, C. Graziano, K. Pysden, Y. Crow +3 more
2012Developmental Medicine & Child Neurology19 citations Open access
Semantic Scholar
Neonatal hypertonia – a diagnostic challenge
A. Hart, Ruchi Sharma, Christopher D. Rittey, S. Mordekar
2015Developmental Medicine & Child Neurology17 citations Open access
Semantic Scholar
Home video telemetry in children: A comparison to inpatient video telemetry.
Sophie Carlson, R. Kandler, D. Moorhouse, A. Ponnusamy +2 more
2018Seizure16 citations Open access
Semantic Scholar
Feed-induced Dystonias in Children With Severe Central Nervous System Disorders
S. Mordekar, M. Velayudhan, D. Campbell
2017Journal of Pediatric Gastroenterology and Nutrition - JPGN15 citations
Semantic Scholar
Outcome of children with hyperventilation‐induced high‐amplitude rhythmic slow activity with altered awareness
Alexander Barker, J. Ng, C. Rittey, R. Kandler +1 more
2012Developmental Medicine & Child Neurology14 citations
Semantic Scholar
Unilateral periventricular leukomalacia in association with pyruvate dehydrogenase deficiency
Ruchi Sharma, M. Sharrard, D. Connolly, S. Mordekar
2012Developmental Medicine & Child Neurology11 citations
Semantic Scholar
Stroke in a child with neurofibromatosis type 2.
J. Ng, S. Mordekar, D. Connolly, P. Baxter
2009European journal of paediatric neurology11 citations
Semantic Scholar
Diffusion‐weighted imaging and magnetic resonance spectroscopy findings in a case of neonatal hypoglycaemia
R. Musson, R. Batty, S. Mordekar, I. Wilkinson +2 more
2009Developmental Medicine & Child Neurology11 citations
Semantic Scholar
Intrathecal baclofen pumps in the management of hypertonia in childhood: a UK and Ireland wide survey
R. Lodh, S. Amin, A. Ammar, L. Bellis +23 more
2021Archives of Disease in Childhood9 citations Open access
Semantic Scholar
Acute bilateral striatal necrosis with rotavirus gastroenteritis and inborn metabolic predisposition
S. Mordekar, T. Jaspan, M. Sharrard, R. Morton +1 more
2005Developmental Medicine & Child Neurology8 citations Open access
Semantic Scholar
The Encephalopathic Child
O. Abeyakoon, R. Batty, S. Mordekar, A. Raghavan +3 more
2011The Neuroradiology Journal7 citations
Semantic Scholar
The significance of reduced respiratory chain enzyme activities: clinical, biochemical and radiological associations.
S. Mordekar, P. Guthrie, J. R. Bonham, S. Olpin +2 more
2006European journal of paediatric neurology7 citations
Semantic Scholar
Genotype-phenotype variability of DARS mutation - case reports of a trio of siblings
Ong T. Min, J. Willoughby, D. Connolly, S. Mordekar +2 more
2020European Journal of Medical Case Reports6 citations
Semantic Scholar
Cerebral cavernous malformation: clinical report of two families with variable phenotype associated with KRIT1 mutation.
M. Balasubramanian, V. Jain, R. Glover, L. Robertson +1 more
2013European journal of paediatric neurology6 citations
Semantic Scholar
Retention rate of Gabapentin in children with intractable epilepsies at 1 year.
J. Mills, N. Ruslan, T. Lewis, K. Mughal +9 more
2012Seizure6 citations Open access
Semantic Scholar
Tigroid pattern of cerebral white matter involvement in chromosome 6p25 deletion syndrome with concomitant 5p15 duplication
M. Balasubramanian, Kath Smith, S. Williams, P. Griffiths +2 more
2012Journal of Pediatric Genetics5 citations Open access
Semantic Scholar
O13 Working definition of gastrointestinal dystonia of severe neuro-disability; outcome of the BSPGHAN/BAPM/BAPS/APPM/BPNA appropriateness panel
Andrew Barclay, S. Meade, Catherine Richards, Timothy Warlow +25 more
2022Wednesday 26th April 20224 citations
Semantic Scholar
Glioblastoma multiforme incorrectly diagnosed as ADEM in children
S. Mordekar, C. Rittey, T. Jaspan, D. Connolly +1 more
2008Journal of Pediatric Neurology online4 citations
Semantic Scholar
Post‐Treatment Movement Disorder in a Child with Late‐onset Cobalamin Deficiency
A. Fadilah, P. Baxter, P. Sarrigiannis, S. Sengupta +2 more
2021Movement Disorders Clinical Practice3 citations Open access
Semantic Scholar
Acquired Vitamin B12 Deficiency in Infancy
A. Fadilah, R. Musson, S. Mordekar
2018Journal of Pediatric Neurology online3 citations
Semantic Scholar
CT and MR Imaging of the Encephalopathic Child
H. Warner, R. Batty, A. Hart, S. Mordekar +3 more
20183 citations
Semantic Scholar
‘Cerebral palsy’ due to mitochondrial cytopathy
S. Mordekar, PS Baxter
2004Journal of Paediatrics and Child Health3 citations
Semantic Scholar
Vitamin B12 deficiency in infants secondary to maternal deficiency: A case series of seven infants
A. Fadilah, R. Musson, M. Ong, A. Desurkar +1 more
20172 citations
Semantic Scholar
Fifteen-minute consultation: Approach to the child with an acute confusional state
M. Prasad, A. Seal, S. Mordekar
2016Archives of Disease in Childhood: Education & Practice Edition2 citations
Semantic Scholar
Reversible parainfectious bilateral "striatal necrosis".
S. Nandish, Rafeh Khan, D. Connolly, C. Rittey +1 more
2012Pediatric Neurology2 citations
Semantic Scholar
Favorable outcome from alpha coma in a 15-year-old with traumatic brain injury
S. Mordekar, M. Prasad, N. J. Smith, H. Vyas +3 more
2012Journal of Pediatric Neurology online2 citations
Semantic Scholar
Reversible basal ganglia signal changes associated with vigabatrin treatment in infants with epilepsy
S. Mordekar, C. Rittey, D. Connolly, P. Baxter
2011Journal of Pediatric Neurology online2 citations
Semantic Scholar

Frequent co-authors

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D. Connolly×12
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D. Connolly — researcher profile on SciRah
M. Kurian×5
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M. Kurian — researcher profile on SciRah
R. Batty×5
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R. Batty — researcher profile on SciRah
C. Rittey×5
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C. Rittey — researcher profile on SciRah

M. Balasubramanian

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A. Fadilah — researcher profile on SciRah

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A. Hart — researcher profile on SciRah

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M. Sharrard — researcher profile on SciRah

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P. Baxter — researcher profile on SciRah

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E. Wassmer — researcher profile on SciRah

Pankaj B. Agrawal×3

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D. Lumsden — researcher profile on SciRah