Anna Kaminska

Anna Kaminska publication distribution in Neuroscience in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Neuroscience in 2026. The highlighted bar marks where Anna Kaminska sits on this spectrum.

Anna Kaminska D-index placement in Neuroscience in 2026

The chart shows the D-index (discipline H-index) distribution of Neuroscience scientists ranked by Research.com in 2026. The highlighted bar marks where Anna Kaminska sits on this spectrum.

Overview

Best Publications

• Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy

  Renzo Guerrini;Charlotte Dravet;Pierre Genton;Anna Belmonte

  550
  Citations

• De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.

  Giulia Barcia;Matthew R Fleming;Aline Deligniere;Valeswara-Rao Gazula

  547
  Citations

• Rapid Cortical Oscillations and Early Motor Activity in Premature Human Neonate

  Mathieu Milh;Anna Kaminska;Catherine Huon;Alexandre Lapillonne

  306
  Citations

• A conserved switch in sensory processing prepares developing neocortex for vision

  Matthew T. Colonnese;Anna Kaminska;Anna Kaminska;Marat Minlebaev;Mathieu Milh

  300
  Citations

• The three stages of epilepsy in patients with CDKL5 mutations.

  Nadia Bahi-Buisson;Nadia Bahi-Buisson;Anna Kaminska;Anna Kaminska;Nathalie Boddaert;Nathalie Boddaert;Marlène Rio

  220
  Citations

• Genome search for susceptibility loci of common idiopathic generalised epilepsies

  Thomas Sander;Herbert Schulz;Kathrin Saar;Elena Gennaro

  218
  Citations

• Delineation of cryptogenic Lennox-Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis.

  A Kaminska;A Ickowicz;P Plouin;M.F Bru

  173
  Citations

• Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.

  Mathieu Milh;Nathalie Villeneuve;Mondher Chouchane;Anna Kaminska

  165
  Citations

• Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females.

  Christel Depienne;Oriane Trouillard;Delphine Bouteiller;Isabelle Gourfinkel-An;Isabelle Gourfinkel-An

  157
  Citations

• Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts

  F Molinari;A Kaminska;G Fiermonte;N Boddaert

  139
  Citations

• The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 1)†

  Michalis Koutroumanidis;Alexis Arzimanoglou;Roberto Caraballo;Sushma Goyal

  128
  Citations

• A brain atlas of axonal and synaptic delays based on modelling of cortico-cortical evoked potentials

  Unknown

  113
  Citations

• Normal EEG in childhood: from neonates to adolescents.

  M. Eisermann;A. Kaminska;A. Kaminska;M.-L. Moutard;C. Soufflet;C. Soufflet

  110
  Citations

• Ictal SPECT in children with epilepsy: comparison with intracranial EEG and relation to postsurgical outcome.

  A. Kaminska;C. Chiron;D. Ville;G. Dellatolas

  108
  Citations

• Efficacy and safety of abobotulinumtoxinA in spastic lower limb: Randomized trial and extension.

  Jean-Michel Gracies;Alberto Esquenazi;Allison Brashear;Marta Banach

  106
  Citations

• Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2

  Mathieu Milh;Nadia Boutry-Kryza;Julie Sutera-Sardo;Cyril Mignot

  105
  Citations

• Epilepsy in Menkes disease: analysis of clinical stages.

  Nadia Bahi-Buisson;Nadia Bahi-Buisson;Anna Kaminska;Rima Nabbout;Rima Nabbout;Christine Barnerias

  104
  Citations

• Early electro-clinical features may contribute to diagnosis of the anti-NMDA receptor encephalitis in children

  Cyril Gitiaux;Cyril Gitiaux;Hina Simonnet;Monika Eisermann;Monika Eisermann;Dorothee Leunen;Dorothee Leunen

  101
  Citations

• Use of subtraction ictal SPECT co-registered to MRI for optimizing the localization of seizure foci in children.

  Pierre Véra;Anna Kaminska;Cécile Cieuta;Andreas Hollo

  101
  Citations

• LIS1-related isolated lissencephaly: spectrum of mutations and relationships with malformation severity.

  Yoann Saillour;Nathalie Carion;Chloé Quelin;Pierre-Louis Leger

  88
  Citations

• O9 – 2019 Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2

  M Milh;N Boutry-Kryza;J Sutera-Sardo;C Mignot

  0
  Citations