Paul, Lynn K.

• Tusche, Anita; Spunt, Robert P.; et el. (2023) Neural signatures of social inferences predict the number of real-life social contacts and autism severity; Nature Communications; Vol. 14; Art. No. 4399; PMCID PMC10359299; 10.1038/s41467-023-40078-3
• Rouhani, Nina; Stanley, Damian; et el. (2023) Collective events and individual affect shape autobiographical memory; Proceedings of the National Academy of Sciences of the United States of America; Vol. 120; No. 29; Art. No. e2221919120; PMCID PMC10629560; 10.1073/pnas.2221919120
• Papini, Santiago; López-Castro, Teresa; et el. (2023) Alcohol, cannabis, and nicotine use have distinct associations with COVID-19 pandemic-related experiences: An exploratory Bayesian network analysis across two timepoints; Drug and Alcohol Dependence; Vol. 248; Art. No. 109929; PMCID PMC10186931; 10.1016/j.drugalcdep.2023.109929
• Su, Judy J.; Paul, Lynn K.; et el. (2023) Verbal problem-solving in agenesis of the corpus callosum: Analysis using semantic similarity; Neuropsychology; Vol. 37; No. 5; 615-620; PMCID PMC10330553; 10.1037/neu0000894
• Su, Judy J.; Paul, Lynn K.; et el. (2023) Verbal problem-solving in agenesis of the corpus callosum: Analysis using semantic similarity; Neuropsychology; 10.1037/neu0000894
• Rusch, Tessa; Han, Yanting; et el. (2023) COVID-Dynamic: a large-scale longitudinal study of socioemotional and behavioral change across the pandemic; Scientific Data; Vol. 10; Art. No. 71; PMCID PMC9897616; 10.1038/s41597-022-01901-6
• López-Castro, Teresa; Papini, Santiago; et el. (2023) Posttraumatic stress disorder symptom trajectories in a 16-month COVID-19 pandemic period; Journal of Traumatic Stress; Vol. 36; No. 1; 180-192; PMCID PMC9880687; 10.1002/jts.22899
• Saltoun, Karin; Adolphs, Ralph; et el. (2022) Dissociable brain structural asymmetry patterns reveal unique phenome-wide profiles; Nature Human Behaviour; 10.1038/s41562-022-01461-0
• Keleş, Ümit; Kliemann, Dorit; et el. (2022) Atypical gaze patterns in autistic adults are heterogeneous across but reliable within individuals; Molecular Autism; Vol. 13; No. 1; Art. No. 39; PMCID PMC9508778; 10.1186/s13229-022-00517-2
• Zhang, Na; Ruan, Mindi; et el. (2022) Discriminative Few Shot Learning of Facial Dynamics in Interview Videos for Autism Trait Classification; IEEE Transactions on Affective Computing; 10.1109/taffc.2022.3178946
• Kliemann, Dorit; Adolphs, Ralph; et el. (2022) Caltech Conte Center, a multimodal data resource for exploring social cognition and decision-making; Scientific Data; Vol. 9; Art. No. 138; PMCID PMC8971509; 10.1038/s41597-022-01171-2
• Jones, Monika; Harris, William B.; et el. (2022) Knowledge gaps for functional outcomes after multilobar resective and disconnective pediatric epilepsy surgery: Conference Proceedings of the Patient-Centered Stakeholder Meeting 2019; Epileptic Disorders; Vol. 24; No. 1; 50-66; 10.1684/epd.2021.1373
• Renteria-Vazquez, Tiffany; Brown, Warren S.; et el. (2022) Social Inferences in Agenesis of the Corpus Callosum and Autism: Semantic Analysis and Topic Modeling; Journal of Autism and Developmental Disorders; Vol. 52; No. 2; 569-583; PMCID PMC9042290; 10.1007/s10803-021-04957-2
• Mangum, Ryan W.; Miller, Justin S.; et el. (2021) Everyday Executive Function and Self-Awareness in Agenesis of the Corpus Callosum; Journal of the International Neuropsychological Society; Vol. 27; No. 10; 1037-1047; PMCID PMC8744483; 10.1017/s1355617721000096
• Rusch, Tessa; Han, Yanting; et el. (2021) COVID-Dynamic: A large-scale multifaceted longitudinal study of socioemotional and behavioral change across the pandemic; 10.31234/osf.io/75eyx
• Paul, Lynn K.; Pazienza, Shawneen R.; et el. (2021) Alexithymia and somatization in agenesis of the corpus callosum; Social Cognitive and Affective Neuroscience; Vol. 16; No. 10; 1071-1078; PMCID PMC8483281; 10.1093/scan/nsab056
• Brown, Warren S.; Burnett, Karissa A; et el. (2021) Appreciation of Social Norms in Agenesis of the Corpus Callosum; Archives of Clinical Neuropsychology; Vol. 36; No. 7; 1367-1373; PMCID PMC8652238; 10.1093/arclin/acab003
• Charpentier, Caroline J.; Faulkner, Paul; et el. (2021) How representative are neuroimaging samples? Large-scale evidence for trait anxiety differences between fMRI and behaviour-only research participants; Social Congnitive and Affective Neuroscience; Vol. 16; No. 10; 1057-1070; PMCID PMC8483285; 10.1093/scan/nsab057
• Lee, Seung J.; Beam, Danielle E.; et el. (2021) Single-neuron correlate of epilepsy-related cognitive deficits in visual recognition memory in right mesial temporal lobe; Epilepsia; Vol. 62; No. 9; 2082-2093; PMCID PMC8403636; 10.1111/epi.17010
• Kliemann, Dorit; Adolphs, Ralph; et el. (2021) Reorganization of the Social Brain in Individuals with Only One Intact Cerebral Hemisphere; Brain Sciences; Vol. 11; No. 8; Art. No. 965; PMCID PMC8392565; 10.3390/brainsci11080965
• Keleş, Ümit; Kliemann, Dorit; et el. (2021) Atypical gaze patterns in autism are heterogeneous across subjects but reliable within individuals; 10.1101/2021.07.01.450793
• Dubois, Julien; Eberhardt, Frederick; et el. (2020) Personality beyond taxonomy; Nature Human Behaviour; Vol. 4; No. 11; 1110-1117; 10.1038/s41562-020-00989-3
• Brown, Warren S.; Panos, Amanda; et el. (2020) Attention, impulsivity, and vigilance in agenesis of the corpus callosum; Neuropsychology; Vol. 34; No. 7; 744-749; PMCID PMC7989585; 10.1037/neu0000685
• Paradiso, Sergio; Brown, Warren S.; et el. (2020) Integration Between Cerebral Hemispheres Contributes to Defense Mechanisms; Frontiers in Psychology; Vol. 11; Art. No. 1534; PMCID PMC7359856; 10.3389/fpsyg.2020.01534
• Spencer-Smith, Megan; Knight, Jacquelyn L.; et el. (2020) Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations; Developmental Medicine & Child Neurology; Vol. 62; No. 6; 758-762; 10.1111/dmcn.14486
• Lin, Chujun; Keleş, Ümit; et el. (2020) No strong evidence that social network index is associated with gray matter volume from a data-driven investigation; Cortex; Vol. 125; 307-317; PMCID PMC7774327; 10.1016/j.cortex.2020.01.021
• Kliemann, Dorit; Adolphs, Ralph; et el. (2019) Intrinsic Functional Connectivity of the Brain in Adults with a Single Cerebral Hemisphere; Cell Reports; Vol. 29; No. 8; 2398-2407; PMCID PMC6914265; 10.1016/j.celrep.2019.10.067
• Waytz, Adam; Cacioppo, John T.; et el. (2019) Anthropomorphizing without Social Cues Requires the Basolateral Amygdala; Journal of Cognitive Neuroscience; Vol. 31; No. 4; 482-496; 10.1162/jocn_a_01365
• Brown, Warren S. and Paul, Lynn K. (2019) The Neuropsychological Syndrome of Agenesis of the Corpus Callosum; Journal of the International Neuropsychological Society; Vol. 25; No. 3; 324-330; PMCID PMC7989584; 10.1017/S135561771800111X
• Young, Christina M.; Folsom, Renee C.; et el. (2019) Awareness of consequences in agenesis of the corpus callosum: Semantic analysis of responses; Neuropsychology; Vol. 33; No. 2; 275-284; 10.1037/neu0000512
• Dubois, Julien; Galdi, Paola; et el. (2018) A distributed brain network predicts general intelligence from resting-state human neuroimaging data; Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences; Vol. 373; No. 1756; Art. No. 20170284; PMCID PMC6107566; 10.1098/rstb.2017.0284
• Dubois, Julien; Galdi, Paola; et el. (2018) Resting-state functional brain connectivity best predicts the personality dimension of openness to experience; Personality Neuroscience; Vol. 1; Art. No. e6; PMCID PMC6138449; 10.1017/pen.2018.8
• Anderson, Luke B.; Paul, Lynn K.; et el. (2017) Emotional Intelligence in Agenesis of the Corpus Callosum; Archives of Clinical Neuropsychology; Vol. 32; No. 3; 267-279; 10.1093/arclin/acx001
• Wang, Shuo; Fan, Shaojing; et el. (2016) Revealing the world of autism through the lens of a camera; Current Biology; Vol. 26; No. 20; R909-R910; PMCID PMC5549856; 10.1016/j.cub.2016.08.055
• Rehmel, Jamie L.; Brown, Warren S.; et el. (2016) Proverb comprehension in individuals with agenesis of the corpus callosum; Brain and Language; Vol. 160; 21-29; 10.1016/j.bandl.2016.07.001
• Paul, Lynn K.; Erickson, Roger L.; et el. (2016) Learning and memory in individuals with agenesis of the corpus callosum; Neuropsychologia; Vol. 86; 183-192; 10.1016/j.neuropsychologia.2016.04.013
• Kennedy, Daniel P.; Paul, Lynn K.; et el. (2015) Brain Connectivity in Autism: The Significance of Null Findings; Biological Psychiatry; Vol. 78; No. 2; 81-82; 10.1016/j.biopsych.2015.05.002
• Demopoulos, Carly; Yu, Nina; et el. (2015) Corpus callosum in cognitive and sensory processing: insights into autism; Future Neurology; Vol. 10; No. 2; 147-160; 10.2217/fnl.14.70
• Bridgman, Matthew W.; Brown, Warren S.; et el. (2014) Facial emotion recognition in agenesis of the corpus callosum; Journal of Neurodevelopmental Disorders; Vol. 6; Art. No. 32; PMCID PMC4335392; 10.1186/1866-1955-6-32
• Tyszka, J. Michael; Kennedy, Daniel P.; et el. (2014) Largely Typical Patterns of Resting-State Functional Connectivity in High-Functioning Adults with Autism; Cerebral Cortex; Vol. 24; No. 7; 1894-1905; PMCID PMC4051895; 10.1093/cercor/bht040
• Erickson, Roger L.; Paul, Lynn K.; et el. (2014) Verbal learning and memory in agenesis of the corpus callosum; Neuropsychologia; Vol. 60; 121-130; PMCID PMC4337878; 10.1016/j.neuropsychologia.2014.06.003
• Paul, Lynn K.; Corsello, Christina; et el. (2014) Agenesis of the corpus callosum and autism: a comprehensive comparison; Brain; Vol. 137; No. 6; 1813-1829; PMCID PMC4072909; 10.1093/brain/awu070
• Gläscher, Jan; Adolphs, Ralph; et el. (2012) Lesion mapping of cognitive control and value-based decision making in the prefrontal cortex; Proceedings of the National Academy of Sciences of the United States of America; Vol. 109; No. 36; 14681-14686; PMCID PMC3437894; 10.1073/pnas.1206608109
• Hinkley, Leighton B. N.; Marco, Elysa J.; et el. (2012) The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing; PLoS ONE; Vol. 7; No. 8; e39804; PMCID PMC3411722; 10.1371/journal.pone.0039804
• Brown, Warren S.; Anderson, Luke B.; et el. (2012) Decision-Making in Individuals with Agenesis of the Corpus Callosum: Expectancy-Valence in the Iowa Gambling Task; Archives of Clinical Neuropsychology; Vol. 27; No. 5; 532-544; 10.1093/arclin/acs052
• Paul, Lynn K. and Tyszka, J. Michael (2012) How important is the corpus callosum in resting-state networks?; Future Neurology; Vol. 7; No. 3; 231-234; 10.2217/fnl.12.17
• Marco, Elysa J.; Harrell, Kathryn M.; et el. (2012) Processing Speed Delays Contribute to Executive Function Deficits in Individuals with Agenesis of the Corpus Callosum; Journal of the International Neuropsychological Society; Vol. 18; No. 3; 521-529; PMCID PMC3605885; 10.1017/S1355617712000045
• Tyszka, J. Michael; Kennedy, Daniel P.; et el. (2011) Intact Bilateral Resting-State Networks in the Absence of the Corpus Callosum; Journal of Neuroscience; Vol. 31; No. 42; 15154-15162; PMCID PMC3221732; 10.1523/JNEUROSCI.1453-11.2011
• Paul, Lynn K. (2011) Developmental malformation of the corpus callosum: a review of typical callosal development and examples of developmental disorders with callosal involvement; Journal of Neurodevelopmental Disorders; Vol. 3; No. 1; 3-27; PMCID PMC3163989; 10.1007/s11689-010-9059-y
• Paul, Lynn K.; Corsello, Christina; et el. (2010) Does bilateral damage to the human amygdala produce autistic symptoms?; Journal of Neurodevelopmental Disorders; Vol. 2; No. 3; 165-173; PMCID PMC2914867; 10.1007/s11689-010-9056-1
• Gläscher, J.; Rudrauf, D.; et el. (2010) Distributed neural system for general intelligence revealed by lesion mapping; Proceedings of the National Academy of Sciences of the United States of America; Vol. 107; No. 10; 4705-4709; PMCID PMC2842050; 10.1073/pnas.0910397107
• Symington, Scott H.; Paul, Lynn K.; et el. (2010) Social cognition in individuals with agenesis of the corpus callosum; Social Neuroscience; Vol. 5; No. 3; 296-308; 10.1080/17470910903462419
• Turk, Anne A.; Brown, Warren S.; et el. (2010) Social narratives in agenesis of the corpus callosum: Linguistic analysis of the Thematic Apperception Test; Neuropsychologia; Vol. 48; No. 1; 43-50; 10.1016/j.neuropsychologia.2009.08.009
• Mueller, Kendra L. Oakes; Marion, Sarah DeBoard; et el. (2009) Bimanual motor coordination in agenesis of the corpus callosum; Behavioral Neuroscience; Vol. 123; No. 5; 1000-1011; 10.1037/a0016868
• Gläscher, Jan; Tranel, Daniel; et el. (2009) Lesion mapping of cognitive abilities linked to intelligence; Neuron; Vol. 61; No. 5; 681-691; PMCID PMC2728583; 10.1016/j.neuron.2009.01.026
• Kaufman, Jason A.; Paul, Lynn K.; et el. (2008) Selective reduction of Von Economo neuron number in agenesis of the corpus callosum; Acta Neuropathologica; Vol. 116; No. 5; 479-489; 10.1007/s00401-008-0434-7
• Badaruddin, Denise H.; Andrews, Glena L.; et el. (2007) Social and Behavioral Problems of Children with Agenesis of the Corpus Callosum; Child Psychiatry and Human Development; Vol. 38; No. 4; 287-302; 10.1007/s10578-007-0065-6
• Paul, Lynn K.; Brown, Warren S.; et el. (2007) Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity; Nature Reviews Neuroscience; Vol. 8; No. 4; 287-299; 10.1038/nrn2107
• Paul, Lynn K.; Lautzenhiser, Aaron; et el. (2006) Emotional arousal in agenesis of the corpus callosum; International Journal of Psychophysiology; Vol. 61; No. 1; 47-56; 10.1016/j.ijpsycho.2005.10.017
• Brown, Warren S.; Symington, Melissa; et el. (2005) Paralinguistic processing in children with callosal agenesis: emergence of neurolinguistic deficits; Brain and Language; Vol. 93; No. 2; 135-139; 10.1016/j.bandl.2004.09.003
• Brown, Warren S.; Paul, Lynn K.; et el. (2005) Comprehension of humor in primary agenesis of the corpus callosum; Neuropsychologia; Vol. 43; No. 6; 906-916; 10.1016/j.neuropsychologia.2004.09.008
• Paul, Lynn K.; Schieffer, Beatrix; et el. (2004) Social processing deficits in agenesis of the corpus callosum: narratives from the Thematic Apperception Test; Archives of Clinical Neuropsychology; Vol. 19; No. 2; 215-225; 10.1016/S0887-6177(03)00024-6
• Lee, Gregory P.; Meador, Kimford J.; et el. (2004) Neural Substrates of Emotion as Revealed by Functional Magnetic Resonance Imaging; Cognitive and Behavioral Neurology; Vol. 17; No. 1; 9-17; 10.1097/00146965-200403000-00002
• Paul, Lynn K.; Van Lancker-Sidtis, Diana; et el. (2003) Communicative deficits in agenesis of the corpus callosum: Nonliteral language and affective prosody; Brain and Language; Vol. 85; No. 2; 313-324; 10.1016/S0093-934X(03)00062-2
• Hines, Robert J.; Paul, Lynn K.; et el. (2002) Spatial attention in agenesis of the corpus callosum: shifting attention between visual fields; Neuropsychologia; Vol. 40; No. 11; 1804-1814; 10.1016/S0028-3932(02)00032-5
• Boone, Kyle Brauer; Swerdloff, Ronald S.; et el. (2001) Neuropsychological profiles of adults with Klinefelter syndrome; Journal of the International Neuropsychological Society; Vol. 7; No. 4; 446-456; 10.1017/s1355617701744013
• Brown, Warren S.; Thrasher, Ellen D.; et el. (2001) Interhemispheric Stroop effects in partial and complete agenesis of the corpus callosum; Journal of the International Neuropsychological Society; Vol. 7; No. 3; 302-311; 10.1017/s1355617701733048
• Brown, Warren S.; Thrasher, Ellen D.; et el. (2001) Interhemispheric Stroop effects in partial and complete agenesis of the corpus callosum; Journal of the International Neuropsychological Society; Vol. 7; No. 3; 302-311; 10.1017/S1355617701733048
• Brown, Warren S. and Paul, Lynn K. (2000) Cognitive and psychosocial deficits in agenesis of the corpus callosum with normal intelligence; Cognitive Neuropsychiatry; Vol. 5; No. 2; 135-137; 10.1080/135468000395781