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Number of items: 16.


Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191
(2017) Advanced Magnetic Resonance Imaging and Quantitative Analysis Approaches in Patients with Refractory Focal Epilepsy. PhD thesis, University of Liverpool.


McKavanagh, Andrea ORCID: 0000-0003-3053-3564, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Chen, Yachin ORCID: 0000-0002-6623-8658, Denby, Christine, Bracewell, Martyn, Das, Kumar, De Bezenac, Christophe, Marson, Anthony G ORCID: 0000-0002-6861-8806, Taylor, Peter N and Keller, Simon S ORCID: 0000-0001-5247-9795
(2022) Altered Structural Brain Networks in Refractory and Nonrefractory Idiopathic Generalized Epilepsy. BRAIN CONNECTIVITY, 12 (6). pp. 549-560.


Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, McKavanagh, Andrea ORCID: 0000-0003-3053-3564, Alonazi, Batil, Bryant, Lorna, Das, Kumar, Wieshmann, Udo C, Marson, Anthony G ORCID: 0000-0002-6861-8806, Taylor, Peter N and Keller, Simon S ORCID: 0000-0001-5247-9795
(2021) Altered structural connectome in non-lesional newly diagnosed focal epilepsy: Relation to pharmacoresistance. NeuroImage: Clinical, 29. p. 102564.


Gleichgerrcht, Ezequiel, Munsell, Brent C, Alhusaini, Saud, Alvim, Marina KM, Bargalló, Núria, Bender, Benjamin, Bernasconi, Andrea, Bernasconi, Neda, Bernhardt, Boris, Blackmon, Karen
et al (show 56 more authors) (2021) Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: a worldwide ENIGMA-Epilepsy study. NeuroImage: Clinical, 31. p. 102765.


Brownhill, Daniel, Chen, Yachin ORCID: 0000-0002-6623-8658, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, de Bezenac, Christophe, Denby, Christine, Bracewell, Martyn, Biswas, Shubhabrata, Das, Kumar, Marson, Anthony G ORCID: 0000-0002-6861-8806 and Keller, Simon S ORCID: 0000-0001-5247-9795
(2021) Automated subcortical volume estimation from 2D MRI in epilepsy and implications for clinical trials. Neuroradiology, 64 (5). pp. 935-947.


Sisodiya, Sanjay M, Whelan, Christopher D, Hatton, Sean N, Huynh, Khoa, Altmann, Andre, Ryten, Mina, Vezzani, Annamaria, Caligiuri, Maria Eugenia, Labate, Angelo, Gambardella, Antonio
et al (show 62 more authors) (2022) The ENIGMA-Epilepsy working group: Mapping disease from large data sets. HUMAN BRAIN MAPPING, 43 (1). pp. 113-128.


Lopez, Seymour M, Aksman, Leon M, Oxtoby, Neil P, Vos, Sjoerd B, Rao, Jun, Kaestner, Erik, Alhusaini, Saud, Alvim, Marina, Bender, Benjamin, Bernasconi, Andrea
et al (show 66 more authors) (2022) Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data. EPILEPSIA, 63 (8). pp. 2081-2095.


Bryant, Lorna, McKinnon, Emilie T, Taylor, James A, Jensen, Jens H, Bonilha, Leonardo, de Bezenac, Christophe, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Adan, Guleed ORCID: 0000-0001-7340-4207, Wieshmann, Udo C, Biswas, Shubhabrata
et al (show 2 more authors) (2021) Fiber ball white matter modeling in focal epilepsy. HUMAN BRAIN MAPPING, 42 (8). pp. 2490-2507.


Pegg, Emily J, McKavanagh, Andrea, Bracewell, R Martyn, Chen, Yachin ORCID: 0000-0002-6623-8658, Das, Kumar, Denby, Christine, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Laiou, Petroula, Marson, Anthony ORCID: 0000-0002-6861-8806, Mohanraj, Rajiv
et al (show 2 more authors) (2021) Functional network topology in drug resistant and well-controlled idiopathic generalized epilepsy: a resting state functional MRI study. BRAIN COMMUNICATIONS, 3 (3). fcab196-.


McKavanagh, Andrea, Ridzuan-Allen, Adam, Kreilkamp, Barbara AK, Chen, Yachin, Manjón, José V, Coupé, Pierrick, Bracewell, Martyn, Das, Kumar, Taylor, Peter N, Marson, Anthony G
et al (show 1 more authors) (2023) Midbrain structure volume, estimated myelin and functional connectivity in idiopathic generalised epilepsy. Epilepsy & Behavior, 140. p. 109084.


Chen, Yachin ORCID: 0000-0002-6623-8658, Fallon, Nicholas ORCID: 0000-0003-1451-6983, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Denby, Christine, Bracewell, Martyn, Das, Kumar, Pegg, Emily, Mohanraj, Rajiv, Marson, Anthony G ORCID: 0000-0002-6861-8806 and Keller, Simon S ORCID: 0000-0001-5247-9795
(2021) Probabilistic mapping of thalamic nuclei and thalamocortical functional connectivity in idiopathic generalised epilepsy. HUMAN BRAIN MAPPING, 42 (17). pp. 5648-5664.


Larivière, Sara, Royer, Jessica, Rodríguez-Cruces, Raúl, Paquola, Casey, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon S ORCID: 0000-0001-5247-9795, Cendes, Fernando, Yasuda, Clarissa L
et al (show 64 more authors) (2022) Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression. Nature Communications, 13 (1). 4320-.


Park, Bo-yong, Lariviere, Sara, Rodriguez-Cruces, Raul, Royer, Jessica, Tavakol, Shahin, Wang, Yezhou, Caciagli, Lorenzo, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis
et al (show 77 more authors) (2022) Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy. BRAIN, 145 (4). pp. 1285-1298.


Hatton, Sean N, Huynh, Khoa H, Bonilha, Leonardo, Abela, Eugenio, Alhusaini, Saud, Altmann, Andre, Alvim, Marina KM, Balachandra, Akshara R, Bartolini, Emanuele, Bender, Benjamin
et al (show 66 more authors) (2020) White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study. Brain, 143 (8). pp. 2454-2473.


Hatton, Sean N ORCID: 0000-0002-9149-8726, Huynh, Khoa H, Bonilha, Leonardo, Abela, Eugenio ORCID: 0000-0002-9356-1450, Alhusaini, Saud, Altmann, Andre ORCID: 0000-0002-9265-2393, Alvim, Marina KM, Balachandra, Akshara R, Bartolini, Emanuele, Bender, Benjamin
et al (show 66 more authors) (2020) White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study. Brain : a journal of neurology, 143 (8). 2454 - 2473.


Heide, Ev-Christin, Puk, Oliver, Biskup, Saskia, Krahn, Arne, Rauf, Erik, Kreilkamp, Barbara AK ORCID: 0000-0001-6881-5191, Paulus, Walter and Focke, Niels K
(2021) A novel likely pathogenic heterozygous <i>HECW2</i> missense variant in a family with variable expressivity of neurodevelopmental delay, hypotonia, and epileptiform EEG patterns. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 185 (12). pp. 3838-3843.

This list was generated on Sat Apr 6 21:28:12 2024 BST.