Connection

ALICA GOLDMAN to Humans

This is a "connection" page, showing publications ALICA GOLDMAN has written about Humans.
Connection Strength

0.175
  1. Prophecy or empiricism? Clinical value of predicting versus determining genetic variant functions. Epilepsia. 2023 11; 64(11):2909-2913.
    View in: PubMed
    Score: 0.022
  2. SLC35A2-Related Epilepsy: Global Neuronal Consequences of a Focal Disruption in Glycosylation. Neurology. 2023 01 31; 100(5):225-226.
    View in: PubMed
    Score: 0.021
  3. Peri-ictal Brainstem-Driven Posturing and Its Meaning. Neurology. 2021 01 19; 96(3):89-90.
    View in: PubMed
    Score: 0.019
  4. De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder. Am J Hum Genet. 2020 04 02; 106(4):438-452.
    View in: PubMed
    Score: 0.018
  5. Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019 01 08; 92(2):e108-e114.
    View in: PubMed
    Score: 0.016
  6. Brainstem network disruption: A pathway to sudden unexplained death in epilepsy? Hum Brain Mapp. 2018 12; 39(12):4820-4830.
    View in: PubMed
    Score: 0.016
  7. Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia. 2016 Jan; 57 Suppl 1:17-25.
    View in: PubMed
    Score: 0.013
  8. Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006 Feb; 21(2):93-8.
    View in: PubMed
    Score: 0.007
  9. Benchmarking signal quality and spatiotemporal distribution of interictal spikes in prolonged human iEEG recordings using CorTec wireless brain interchange. Sci Rep. 2024 02 08; 14(1):2652.
    View in: PubMed
    Score: 0.006
  10. Epigenetic genes and epilepsy - emerging mechanisms and clinical applications. Nat Rev Neurol. 2022 09; 18(9):530-543.
    View in: PubMed
    Score: 0.005
  11. Nine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy. Neurology. 2020 09 01; 95(9):e1244-e1256.
    View in: PubMed
    Score: 0.005
  12. Epigenetics explained: a topic "primer" for the epilepsy community by the ILAE Genetics/Epigenetics Task Force. Epileptic Disord. 2020 Apr 01; 22(2):127-141.
    View in: PubMed
    Score: 0.004
  13. De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Cold Spring Harb Mol Case Stud. 2019 06; 5(3).
    View in: PubMed
    Score: 0.004
  14. Channelopathy as a SUDEP Biomarker in Dravet Syndrome Patient-Derived Cardiac Myocytes. Stem Cell Reports. 2018 09 11; 11(3):626-634.
    View in: PubMed
    Score: 0.004
  15. Brain-responsive neurostimulation in patients with medically intractable seizures arising from eloquent and other neocortical areas. Epilepsia. 2017 06; 58(6):1005-1014.
    View in: PubMed
    Score: 0.004
  16. Lateralization of mesial temporal lobe epilepsy with chronic ambulatory electrocorticography. Epilepsia. 2015 Jun; 56(6):959-67.
    View in: PubMed
    Score: 0.003
  17. Long-term treatment with responsive brain stimulation in adults with refractory partial seizures. Neurology. 2015 Feb 24; 84(8):810-7.
    View in: PubMed
    Score: 0.003
  18. Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 2013 Mar 19; 80(12):1078-85.
    View in: PubMed
    Score: 0.003
  19. To share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011 Nov; 13(11):948-55.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.