2013 - BPS Barbara Wilson Lifetime Achievement Award, British Psychological Society
Fellow of The Academy of Medical Sciences, United Kingdom
His primary areas of study are Neuroscience, KE family, Language disorder, FOXP2 and Episodic memory. Many of his studies on Neuroscience apply to Audiology as well. His KE family course of study focuses on FOXP2 Gene and Mutation.
His Language disorder research is within the category of Cognition. His FOXP2 research includes themes of Communication disorder and Caudate nucleus. The Episodic memory study combines topics in areas such as Cognitive psychology, Amnesia, Recall, Recognition memory and Semantic memory.
Faraneh Vargha-Khadem mostly deals with Neuroscience, Cognitive psychology, Audiology, Cognition and Amnesia. His Neuroscience study typically links adjacent topics like KE family. The KE family study which covers Communication disorder that intersects with FOXP2.
His study in Audiology is interdisciplinary in nature, drawing from both Developmental psychology and Hemispherectomy. His research investigates the link between Cognition and topics such as Pediatrics that cross with problems in Intelligence quotient. His Amnesia research is multidisciplinary, incorporating perspectives in Memory disorder, Semantic memory and Episodic memory.
Faraneh Vargha-Khadem focuses on Neuroscience, Cognition, Cognitive psychology, Hippocampus and Hippocampal formation. He regularly links together related areas like FOXP2 in his Neuroscience studies. His studies deal with areas such as Test, Epilepsy surgery, Epilepsy and Pediatrics as well as Cognition.
His work in the fields of Cognitive psychology, such as Mnemonic, overlaps with other areas such as Conjunction. The study incorporates disciplines such as Recall and Thalamus in addition to Hippocampus. His Episodic memory research incorporates elements of Semantic memory and Amnesia.
Neuroscience, Hippocampal formation, Episodic memory, Cognitive psychology and Hippocampus are his primary areas of study. His biological study spans a wide range of topics, including White matter and Diffusion MRI. As part of his studies on Episodic memory, Faraneh Vargha-Khadem frequently links adjacent subjects like Semantic memory.
His Semantic memory research is multidisciplinary, relying on both Anterior temporal lobectomy, Temporal lobe, Audiology, Verbal memory and Recognition memory. His work deals with themes such as Baddeley's model of working memory, Cognition, KE family and Speech production, which intersect with Cognitive psychology. Faraneh Vargha-Khadem combines subjects such as Recall, Mnemonic and Amnesia with his study of Hippocampus.
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A forkhead-domain gene is mutated in a severe speech and language disorder
Cecilia S. L. Lai;Simon E. Fisher;Jane A. Hurst;Faraneh Vargha-Khadem.
Nature (2001)
Differential effects of early hippocampal pathology on episodic and semantic memory.
F. Vargha-Khadem;D. G. Gadian;K. E. Watkins;A. Connelly.
Science (1997)
Localisation of a gene implicated in a severe speech and language disorder
Simon E. Fisher;Faraneh Vargha-Khadem;Kate E. Watkins;Anthony P. Monaco.
Nature Genetics (1998)
Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
Faraneh Vargha-Khadem;Kate Watkins;Katie Alcock;Paul Fletcher.
Proceedings of the National Academy of Sciences of the United States of America (1995)
FOXP2 and the neuroanatomy of speech and language
Faraneh Vargha-Khadem;David G. Gadian;Andrew Copp;Mortimer Mishkin.
Nature Reviews Neuroscience (2005)
Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia
Kate E. Watkins;Nina Dronkers;F. Vargha-Khadem.
Brain (2002)
Neural basis of an inherited speech and language disorder
F. Vargha-Khadem;K. E. Watkins;C. J. Price;J. Ashburner.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits
Kay D. MacDermot;Elena Bonora;Nuala Sykes;Anne Marie Coupe.
American Journal of Human Genetics (2005)
MRI analysis of an inherited speech and language disorder: structural brain abnormalities
Kate E. Watkins;F. Vargha-Khadem;J. Ashburner;R. E. Passingham.
Brain (2002)
Language fMRI abnormalities associated with FOXP2 gene mutation
Frédérique Liégeois;Frédérique Liégeois;Torsten Baldeweg;Torsten Baldeweg;Alan Connelly;Alan Connelly;David G Gadian;David G Gadian.
Nature Neuroscience (2003)
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