Elysa Marco, MD

Title(s)Research Affiliate, Cio
SchoolChancellor/EVC/FAS
AddressLocation Required, #001
Varies CA 00000
Phone415-860-5421
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    Collapse Biography 
    Collapse Education and Training
    University of California, San Francisco Residency School of Medicine
    University of California, San FranciscoM.D.2000 School of Medicine

    Collapse Overview 
    Collapse Overview
    Elysa Marco is a cognitive and behavioral child neurologist. She cares for children with all types of neurologic concerns, however, she specializes in the evaluation and treatment of children with cognitive, sensory, and behavioral challenges. Dr. Marco participates in the care of children at Cortica Healthcare in Marin county (San Rafael).

    Dr. Marco also has an active neuroscience collaboration at UCSF that focuses on understanding and finding treatments for individuals with neurodevelopmental disorders. Her research is based on a thorough cognition and sensory evaluation of each child combined with innovative functional imaging to better understand how children's brains process sound, touch, and visual information. Her current research involves individuals with autism disorders, sensory processing disorders, neuroanatomic disorders (such as agenesis of the corpus callosum) and specific genetic disorders (such as 16p11.2 copy number variations.) In addition, she is an active collaborator with investigators studying the effects of autism on maternal health and the neural underpinnings of Tourette's Syndrome. Dr. Marco's lab is also combining structural and functional brain imaging with computer-based training interventions to determine if computer games can help children resist distracting information and improve visual motor planning. The overarching goal of Dr. Marco's research is to use basic science findings to create beneficial treatments for children.

    Dr. Marco received her BA in psychology at the University of Pennsylvania and then obtained her MD at the University of California, San Francisco. She continued her residency training at UCSF in pediatrics, neurology, and child neurology. In addition, she completed a cognitive and behavioral fellowship with an emphasis on the genetics of cognitive impairment. She was on the UCSF faculty from 2005-2019 and continues as an active clinician, researcher, and educator at Cortica Healthcare.

    Collapse Research 
    Collapse Research Activities and Funding
    Neural Mechanisms of Sensory OverResponsivity
    NIH R01MH116950Jul 8, 2019 - Apr 30, 2024
    Role: Co-Principal Investigator
    Magnetic Source Imaging and Sensory Behavioral Characterization in Autism
    NIH K23MH083890Sep 15, 2008 - Jun 30, 2013
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Examining the latent structure and correlates of sensory reactivity in autism: a multi-site integrative data analysis by the autism sensory research consortium. Mol Autism. 2023 Aug 28; 14(1):31. Williams ZJ, Schaaf R, Ausderau KK, Baranek GT, Barrett DJ, Cascio CJ, Dumont RL, Eyoh EE, Failla MD, Feldman JI, Foss-Feig JH, Green HL, Green SA, He JL, Kaplan-Kahn EA, Keçeli-Kaysili B, MacLennan K, Mailloux Z, Marco EJ, Mash LE, McKernan EP, Molholm S, Mostofsky SH, Puts NAJ, Robertson CE, Russo N, Shea N, Sideris J, Sutcliffe JS, Tavassoli T, Wallace MT, Wodka EL, Woynaroski TG. PMID: 37635263; PMCID: PMC10464466.
      View in: PubMed   Mentions:
    2. An Open-Label Study of Cranial Electrotherapy Stimulation on Behavioral Regulation in a Mixed Neurodevelopmental Clinical Cohort. J Integr Neurosci. 2023 Aug 14; 22(5):119. Brandes-Aitken A, Gerdes M, Hattangadi N, Shapiro KA, Marco EJ. PMID: 37735126.
      View in: PubMed   Mentions:
    3. Neurite orientation dispersion and density imaging of white matter microstructure in sensory processing dysfunction with versus without comorbid ADHD. Front Neurosci. 2023; 17:1136424. Mark IT, Wren-Jarvis J, Xiao J, Cai LT, Parekh S, Bourla I, Lazerwitz MC, Rowe MA, Marco EJ, Mukherjee P. PMID: 37492404; PMCID: PMC10363610.
      View in: PubMed   Mentions:
    4. Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families. Am J Med Genet A. 2023 07; 191(7):1900-1910. Wojcik MH, Srivastava S, Agrawal PB, Balci TB, Callewaert B, Calvo PL, Carli D, Caudle M, Colaiacovo S, Cross L, Demetriou K, Drazba K, Dutra-Clarke M, Edwards M, Genetti CA, Grange DK, Hickey SE, Isidor B, Küry S, Lachman HM, Lavillaureix A, Lyons MJ, Marcelis C, Marco EJ, Martinez-Agosto JA, Nowak C, Pizzol A, Planes M, Prijoles EJ, Riberi E, Rush ET, Russell BE, Sachdev R, Schmalz B, Shears D, Stevenson DA, Wilson K, Jansen S, de Vries BBA, Curry CJ. PMID: 37183572; PMCID: PMC10330231.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    5. Hemispheric lateralization of white matter microstructure in children and its potential role in sensory processing dysfunction. Front Neurosci. 2023; 17:1088052. Parekh SA, Wren-Jarvis J, Lazerwitz M, Rowe MA, Powers R, Bourla I, Cai LT, Chu R, Trimarchi K, Garcia R, Marco EJ, Mukherjee P. PMID: 37139524; PMCID: PMC10149818.
      View in: PubMed   Mentions:
    6. Examining the Latent Structure and Correlates of Sensory Reactivity in Autism: A Multi-site Integrative Data Analysis by the Autism Sensory Research Consortium. Res Sq. 2023 Jan 10. Williams ZJ, Schaaf R, Ausderau KK, Baranek GT, Barrett DJ, Cascio CJ, Dumont RL, Eyoh EE, Failla MD, Feldman JI, Foss-Feig JH, Green HL, Green SA, He JL, Kaplan-Kahn EA, Keçeli-Kaysili B, MacLennan K, Mailloux Z, Marco EJ, Mash LE, McKernan EP, Molholm S, Mostofsky SH, Puts NAJ, Robertson CE, Russo N, Shea N, Sideris J, Sutcliffe JS, Tavassoli T, Wallace MT, Wodka EL, Woynaroski TG. PMID: 36712092; PMCID: PMC9882639.
      View in: PubMed   Mentions:
    7. Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology. HGG Adv. 2023 Jan 12; 4(1):100168. Sobering AK, Bryant LM, Li D, McGaughran J, Maystadt I, Moortgat S, Graham JM, van Haeringen A, Ruivenkamp C, Cuperus R, Vogt J, Morton J, Brasch-Andersen C, Steenhof M, Hansen LK, Adler É, Lyonnet S, Pingault V, Sandrine M, Ziegler A, Donald T, Nelson B, Holt B, Petryna O, Firth H, McWalter K, Zyskind J, Telegrafi A, Juusola J, Person R, Bamshad MJ, Earl D, University of Washington Center for Mendelian Genomics, Chun-Hui Tsai A, Yearwood KR, Marco E, Nowak C, Douglas J, Hakonarson H, Bhoj EJ. PMID: 36583168; PMCID: PMC9792386.
      View in: PubMed   Mentions:
    8. Brief Report: Characterization of Sensory Over-Responsivity in a Broad Neurodevelopmental Concern Cohort Using the Sensory Processing Three Dimensions (SP3D) Assessment. J Autism Dev Disord. 2022 Sep 30. Lazerwitz MC, Rowe MA, Trimarchi KJ, Garcia RD, Chu R, Steele MC, Parekh S, Wren-Jarvis J, Bourla I, Mark I, Marco EJ, Mukherjee P. PMID: 36180667; PMCID: PMC9524317.
      View in: PubMed   Mentions: 3     Fields:    
    9. Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region. Neurol Genet. 2022 Oct; 8(5):e200018. Moufawad El Achkar C, Rosen A, Kessler SK, Steinman KJ, Spence SJ, Ramocki M, Marco EJ, Green Snyder L, Spiro JE, Chung WK, Annapurna P, Sherr EH. PMID: 36531974; PMCID: PMC9756306.
      View in: PubMed   Mentions:
    10. Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology. HGG Adv. 2022 Jul 14; 3(3):100102. Sobering AK, Bryant LM, Li D, McGaughran J, Maystadt I, Moortgat S, Graham JM, van Haeringen A, Ruivenkamp C, Cuperus R, Vogt J, Morton J, Brasch-Andersen C, Steenhof M, Hansen LK, Adler É, Lyonnet S, Pingault V, Sandrine M, Ziegler A, Donald T, Nelson B, Holt B, Petryna O, Firth H, McWalter K, Zyskind J, Telegrafi A, Juusola J, Person R, Bamshad MJ, Earl D, University of Washington Center for Mendelian Genomics, Tsai AC, Yearwood KR, Marco E, Nowak C, Douglas J, Hakonarson H, Bhoj EJ. PMID: 35469323; PMCID: PMC9034099.
      View in: PubMed   Mentions:
    11. Enhancing neural markers of attention in children with ADHD using a digital therapeutic. PLoS One. 2021; 16(12):e0261981. Gallen CL, Anguera JA, Gerdes MR, Simon AJ, Cañadas E, Marco EJ. PMID: 34972140; PMCID: PMC8719702.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCTClinical Trials
    12. Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome. Pediatr Neurol. 2022 01; 126:65-73. Steele JL, Morrow MM, Sarnat HB, Alkhunaizi E, Brandt T, Chitayat DA, DeFilippo CP, Douglas GV, Dubbs HA, Elloumi HZ, Glassford MR, Hannibal MC, Héron B, Kim LE, Marco EJ, Mignot C, Monaghan KG, Myers KA, Parikh S, Quinonez SC, Rajabi F, Shankar SP, Shinawi MS, van de Kamp JJP, Veerapandiyan A, Waldman AT, Graf WD. PMID: 34740135.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    13. Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy. Ann Neurol. 2021 08; 90(2):274-284. Spinelli E, Christensen KR, Bryant E, Schneider A, Rakotomamonjy J, Muir AM, Giannelli J, Littlejohn RO, Roeder ER, Schmidt B, Wilson WG, Marco EJ, Iwama K, Kumada S, Pisano T, Barba C, Vetro A, Brilstra EH, van Jaarsveld RH, Matsumoto N, Goldberg-Stern H, Carney PW, Andrews PI, El Achkar CM, Berkovic S, Rodan LH, Undiagnosed Diseases Network (UDN), McWalter K, Guerrini R, Scheffer IE, Mefford HC, Mandelstam S, Laux L, Millichap JJ, Guemez-Gamboa A, Nairn AC, Carvill GL. PMID: 34185323; PMCID: PMC8324566.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimalsCells
    14. Editorial: Sensory Processing Across the Lifespan: A 25-Year Initiative to Understand Neurophysiology, Behaviors, and Treatment Effectiveness for Sensory Processing. Front Integr Neurosci. 2021; 15:652218. Miller LJ, Marco EJ, Chu RC, Camarata S. PMID: 33897385; PMCID: PMC8063042.
      View in: PubMed   Mentions: 3  
    15. Sustained benefits of cognitive training in children with inattention, three-year follow-up. PLoS One. 2021; 16(2):e0246449. Jurigova BG, Gerdes MR, Anguera JA, Marco EJ. PMID: 33539468; PMCID: PMC7861383.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    16. Altered Cerebellar White Matter in Sensory Processing Dysfunction Is Associated With Impaired Multisensory Integration and Attention. Front Psychol. 2020; 11:618436. Narayan A, Rowe MA, Palacios EM, Wren-Jarvis J, Bourla I, Gerdes M, Brandes-Aitken A, Desai SS, Marco EJ, Mukherjee P. PMID: 33613368; PMCID: PMC7888341.
      View in: PubMed   Mentions: 6  
    17. Expansion of NEUROD2 phenotypes to include developmental delay without seizures. Am J Med Genet A. 2021 04; 185(4):1076-1080. Mis EK, Sega AG, Signer RH, Cartwright T, Ji W, Martinez-Agosto JA, Nelson SF, Palmer CGS, Lee H, Mitzelfelt T, Konstantino M, Undiagnosed Diseases Network, Jeffries L, Khokha MK, Marco E, Martin MG, Lakhani SA. PMID: 33438828; PMCID: PMC8212414.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimals
    18. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. Am J Hum Genet. 2020 10 01; 107(4):727-742. Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Klämbt V, Deutsch K, Wu CW, Kolvenbach CM, Kause F, Ottlewski I, Schneider R, Kitzler TM, Majmundar AJ, Buerger F, Onuchic-Whitford AC, Youying M, Kolb A, Salmanullah D, Chen E, van der Ven AT, Rao J, Ityel H, Seltzsam S, Rieke JM, Chen J, Vivante A, Hwang DY, Kohl S, Dworschak GC, Hermle T, Alders M, Bartolomaeus T, Bauer SB, Baum MA, Brilstra EH, Challman TD, Zyskind J, Costin CE, Dipple KM, Duijkers FA, Ferguson M, Fitzpatrick DR, Fick R, Glass IA, Hulick PJ, Kline AD, Krey I, Kumar S, Lu W, Marco EJ, Wentzensen IM, Mefford HC, Platzer K, Povolotskaya IS, Savatt JM, Shcherbakova NV, Senguttuvan P, Squire AE, Stein DR, Thiffault I, Voinova VY, Somers MJG, Ferguson MA, Traum AZ, Daouk GH, Daga A, Rodig NM, Terhal PA, van Binsbergen E, Eid LA, Tasic V, Rasouly HM, Lim TY, Ahram DF, Gharavi AG, Reutter HM, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Lifton RP, Xu H, Mane SM, Sanna-Cherchi S, Sharrocks AD, Raught B, Fisher SE, Bouchard M, Khokha MK, Shril S, Hildebrandt F. PMID: 32891193; PMCID: PMC7536580.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    19. Heteromeric Assembly of Truncated Neuronal Kv7 Channels: Implications for Neurologic Disease and Pharmacotherapy. Mol Pharmacol. 2020 09; 98(3):192-202. Li J, Maghera J, Lamothe SM, Marco EJ, Kurata HT. PMID: 32580997.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansAnimalsCells
    20. Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD. J Med Genet. 2020 10; 57(10):717-724. Granadillo JL, P A Stegmann A, Guo H, Xia K, Angle B, Bontempo K, Ranells JD, Newkirk P, Costin C, Viront J, Stumpel CT, Sinnema M, Panis B, Pfundt R, Krapels IPC, Klaassens M, Nicolai J, Li J, Jiang Y, Marco E, Canton A, Latronico AC, Montenegro L, Leheup B, Bonnet C, M Amudhavalli S, Lawson CE, McWalter K, Telegrafi A, Pearson R, Kvarnung M, Wang X, Bi W, Rosenfeld JA, Shinawi M. PMID: 32152250.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    21. Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders. Am J Hum Genet. 2019 09 05; 105(3):631-639. Fischer-Zirnsak B, Segebrecht L, Schubach M, Charles P, Alderman E, Brown K, Cadieux-Dion M, Cartwright T, Chen Y, Costin C, Fehr S, Fitzgerald KM, Fleming E, Foss K, Ha T, Hildebrand G, Horn D, Liu S, Marco EJ, McDonald M, McWalter K, Race S, Rush ET, Si Y, Saunders C, Slavotinek A, Stockler-Ipsiroglu S, Telegrafi A, Thiffault I, Torti E, Tsai AC, Wang X, Zafar M, Keren B, Kornak U, Boerkoel CF, Mirzaa G, Ehmke N. PMID: 31353024; PMCID: PMC6731356.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    22. Diffusion tensor tractography in children with sensory processing disorder: Potentials for devising machine learning classifiers. Neuroimage Clin. 2019; 23:101831. Payabvash S, Palacios EM, Owen JP, Wang MB, Tavassoli T, Gerdes M, Brandes-Aitken A, Marco EJ, Mukherjee P. PMID: 31035231; PMCID: PMC6488562.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    23. Brief Report: Pilot Study of a Novel Interactive Digital Treatment to Improve Cognitive Control in Children with Autism Spectrum Disorder and Co-occurring ADHD Symptoms. J Autism Dev Disord. 2019 Apr; 49(4):1727-1737. Yerys BE, Bertollo JR, Kenworthy L, Dawson G, Marco EJ, Schultz RT, Sikich L. PMID: 30569407.
      View in: PubMed   Mentions: 22     Fields:    Translation:Humans
    24. White Matter Connectome Correlates of Auditory Over-Responsivity: Edge Density Imaging and Machine-Learning Classifiers. Front Integr Neurosci. 2019; 13:10. Payabvash S, Palacios EM, Owen JP, Wang MB, Tavassoli T, Gerdes M, Brandes-Aitken A, Mukherjee P, Marco EJ. PMID: 30983979; PMCID: PMC6450221.
      View in: PubMed   Mentions: 2  
    25. De novo and biallelic DEAF1 variants cause a phenotypic spectrum. Genet Med. 2019 09; 21(9):2059-2069. Nabais Sá MJ, Jensik PJ, McGee SR, Parker MJ, Lahiri N, McNeil EP, Kroes HY, Hagerman RJ, Harrison RE, Montgomery T, Splitt M, Palmer EE, Sachdev RK, Mefford HC, Scott AA, Martinez-Agosto JA, Lorenz R, Orenstein N, Berg JN, Amiel J, Heron D, Keren B, Cobben JM, Menke LA, Marco EJ, Graham JM, Pierson TM, Karimiani EG, Maroofian R, Manzini MC, Cauley ES, Colombo R, Odent S, Dubourg C, Phornphutkul C, de Brouwer APM, de Vries BBA, Vulto-vanSilfhout AT. PMID: 30923367.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    26. White Matter Connectome Edge Density in Children with Autism Spectrum Disorders: Potential Imaging Biomarkers Using Machine-Learning Models. Brain Connect. 2019 03; 9(2):209-220. Payabvash S, Palacios EM, Owen JP, Wang MB, Tavassoli T, Gerdes M, Brandes-Aitken A, Cuneo D, Marco EJ, Mukherjee P. PMID: 30661372; PMCID: PMC6444925.
      View in: PubMed   Mentions: 21     Fields:    Translation:Humans
    27. Sensory over-responsivity: parent report, direct assessment measures, and neural architecture. Mol Autism. 2019; 10:4. Tavassoli T, Brandes-Aitken A, Chu R, Porter L, Schoen S, Miller LJ, Gerdes MR, Owen J, Mukherjee P, Marco EJ. PMID: 30740199; PMCID: PMC6360663.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    28. White Matter Microstructure Associations of Cognitive and Visuomotor Control in Children: A Sensory Processing Perspective. Front Integr Neurosci. 2018; 12:65. Brandes-Aitken A, Anguera JA, Chang YS, Demopoulos C, Owen JP, Gazzaley A, Mukherjee P, Marco EJ. PMID: 30692921; PMCID: PMC6339953.
      View in: PubMed   Mentions: 6  
    29. Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction. BMC Med Genomics. 2018 05 25; 11(1):50. Marco EJ, Aitken AB, Nair VP, da Gente G, Gerdes MR, Bologlu L, Thomas S, Sherr EH. PMID: 29801487; PMCID: PMC5970458.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    30. Abnormal age-related cortical folding and neurite morphology in children with developmental dyslexia. Neuroimage Clin. 2018; 18:814-821. Caverzasi E, Mandelli ML, Hoeft F, Watson C, Meyer M, Allen IE, Papinutto N, Wang C, Gandini Wheeler-Kingshott CAM, Marco EJ, Mukherjee P, Miller ZA, Miller BL, Hendren R, Shapiro KA, Gorno-Tempini ML. PMID: 29876267; PMCID: PMC5988019.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    31. Characterizing cognitive and visuomotor control in children with sensory processing dysfunction and autism spectrum disorders. Neuropsychology. 2018 02; 32(2):148-160. Brandes-Aitken A, Anguera JA, Rolle CE, Desai SS, Demopoulos C, Skinner SN, Gazzaley A, Marco EJ. PMID: 29376661.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    32. Magnetoencephalographic Imaging of Auditory and Somatosensory Cortical Responses in Children with Autism and Sensory Processing Dysfunction. Front Hum Neurosci. 2017; 11:259. Demopoulos C, Yu N, Tripp J, Mota N, Brandes-Aitken AN, Desai SS, Hill SS, Antovich AD, Harris J, Honma S, Mizuiri D, Nagarajan SS, Marco EJ. PMID: 28603492; PMCID: PMC5445128.
      View in: PubMed   Mentions: 22  
    33. ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. Neurol Genet. 2017 Jun; 3(3):e148. Alber M, Kalscheuer VM, Marco E, Sherr E, Lesca G, Till M, Gradek G, Wiesener A, Korenke C, Mercier S, Becker F, Yamamoto T, Scherer SW, Marshall CR, Walker S, Dutta UR, Dalal AB, Suckow V, Jamali P, Kahrizi K, Najmabadi H, Minassian BA. PMID: 28589176; PMCID: PMC5446782.
      View in: PubMed   Mentions: 23  
    34. A pilot study to determine the feasibility of enhancing cognitive abilities in children with sensory processing dysfunction. PLoS One. 2017; 12(4):e0172616. Anguera JA, Brandes-Aitken AN, Antovich AD, Rolle CE, Desai SS, Marco EJ. PMID: 28380008; PMCID: PMC5381761.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    35. GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects. J Med Genet. 2017 07; 54(7):460-470. Platzer K, Yuan H, Schütz H, Winschel A, Chen W, Hu C, Kusumoto H, Heyne HO, Helbig KL, Tang S, Willing MC, Tinkle BT, Adams DJ, Depienne C, Keren B, Mignot C, Frengen E, Strømme P, Biskup S, Döcker D, Strom TM, Mefford HC, Myers CT, Muir AM, LaCroix A, Sadleir L, Scheffer IE, Brilstra E, van Haelst MM, van der Smagt JJ, Bok LA, Møller RS, Jensen UB, Millichap JJ, Berg AT, Goldberg EM, De Bie I, Fox S, Major P, Jones JR, Zackai EH, Abou Jamra R, Rolfs A, Leventer RJ, Lawson JA, Roscioli T, Jansen FE, Ranza E, Korff CM, Lehesjoki AE, Courage C, Linnankivi T, Smith DR, Stanley C, Mintz M, McKnight D, Decker A, Tan WH, Tarnopolsky MA, Brady LI, Wolff M, Dondit L, Pedro HF, Parisotto SE, Jones KL, Patel AD, Franz DN, Vanzo R, Marco E, Ranells JD, Di Donato N, Dobyns WB, Laube B, Traynelis SF, Lemke JR. PMID: 28377535; PMCID: PMC5656050.
      View in: PubMed   Mentions: 88     Fields:    Translation:Humans
    36. De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome. Am J Hum Genet. 2017 Apr 06; 100(4):650-658. Jansen S, Geuer S, Pfundt R, Brough R, Ghongane P, Herkert JC, Marco EJ, Willemsen MH, Kleefstra T, Hannibal M, Shieh JT, Lynch SA, Flinter F, FitzPatrick DR, Gardham A, Bernhard B, Ragge N, Newbury-Ecob R, Bernier R, Kvarnung M, Magnusson EA, Wessels MW, van Slegtenhorst MA, Monaghan KG, de Vries P, Veltman JA, Deciphering Developmental Disorders Study, Lord CJ, Vissers LE, de Vries BB. PMID: 28343630; PMCID: PMC5384016.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    37. Chronic stress is associated with reduced circulating hematopoietic progenitor cell number: A maternal caregiving model. Brain Behav Immun. 2017 Jan; 59:245-252. Aschbacher K, Milush JM, Gilbert A, Almeida C, Sinclair E, Epling L, Grenon SM, Marco EJ, Puterman E, Epel E. PMID: 27622676; PMCID: PMC5154768.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    38. 16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort. Am J Med Genet A. 2016 11; 170(11):2943-2955. Steinman KJ, Spence SJ, Ramocki MB, Proud MB, Kessler SK, Marco EJ, Green Snyder L, D'Angelo D, Chen Q, Chung WK, Sherr EH, Simons VIP Consortium. PMID: 27410714.
      View in: PubMed   Mentions: 69     Fields:    Translation:HumansCells
    39. Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications. Hum Brain Mapp. 2016 08; 37(8):2833-48. Chang YS, Owen JP, Pojman NJ, Thieu T, Bukshpun P, Wakahiro ML, Marco EJ, Berman JI, Spiro JE, Chung WK, Buckner RL, Roberts TP, Nagarajan SS, Sherr EH, Mukherjee P. PMID: 27219475; PMCID: PMC6867519.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    40. The Contribution of the Corpus Callosum to Language Lateralization. J Neurosci. 2016 Apr 20; 36(16):4522-33. Hinkley LB, Marco EJ, Brown EG, Bukshpun P, Gold J, Hill S, Findlay AM, Jeremy RJ, Wakahiro ML, Barkovich AJ, Mukherjee P, Sherr EH, Nagarajan SS. PMID: 27098695; PMCID: PMC4837685.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    41. White Matter Microstructure is Associated with Auditory and Tactile Processing in Children with and without Sensory Processing Disorder. Front Neuroanat. 2015; 9:169. Chang YS, Gratiot M, Owen JP, Brandes-Aitken A, Desai SS, Hill SS, Arnett AB, Harris J, Marco EJ, Mukherjee P. PMID: 26858611; PMCID: PMC4726807.
      View in: PubMed   Mentions: 22  
    42. Shared and Divergent Auditory and Tactile Processing in Children with Autism and Children with Sensory Processing Dysfunction Relative to Typically Developing Peers. J Int Neuropsychol Soc. 2015 Jul; 21(6):444-54. Demopoulos C, Brandes-Aitken AN, Desai SS, Hill SS, Antovich AD, Harris J, Marco EJ. PMID: 26145730.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    43. Tourette Syndrome: Complementary Insights from Measures of Cognitive Control, Eyeblink Rate, and Pupil Diameter. Front Psychiatry. 2015; 6:95. Tharp JA, Wendelken C, Mathews CA, Marco EJ, Schreier H, Bunge SA. PMID: 26175694; PMCID: PMC4484341.
      View in: PubMed   Mentions: 9  
    44. Improving the Dermatologic Care of Individuals with Autism: A Review of Relevant Issues and a Perspective. Pediatr Dermatol. 2015 Jul-Aug; 32(4):447-54. Oza VS, Marco E, Frieden IJ. PMID: 25779667.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    45. Individuals with agenesis of the corpus callosum show sensory processing differences as measured by the sensory profile. Neuropsychology. 2015 Sep; 29(5):751-758. Demopoulos C, Arroyo MS, Dunn W, Strominger Z, Sherr EH, Marco E. PMID: 25528608; PMCID: PMC4476955.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    46. Autism and sensory processing disorders: shared white matter disruption in sensory pathways but divergent connectivity in social-emotional pathways. PLoS One. 2014; 9(7):e103038. Chang YS, Owen JP, Desai SS, Hill SS, Arnett AB, Harris J, Marco EJ, Mukherjee P. PMID: 25075609; PMCID: PMC4116166.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    47. Aberrant white matter microstructure in children with 16p11.2 deletions. J Neurosci. 2014 Apr 30; 34(18):6214-23. Owen JP, Chang YS, Pojman NJ, Bukshpun P, Wakahiro ML, Marco EJ, Berman JI, Spiro JE, Chung WK, Buckner RL, Roberts TP, Nagarajan SS, Sherr EH, Mukherjee P, Simons VIP Consortium. PMID: 24790192; PMCID: PMC6608115.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansCells
    48. Autism traits in the RASopathies. J Med Genet. 2014 Jan; 51(1):10-20. Adviento B, Corbin IL, Widjaja F, Desachy G, Enrique N, Rosser T, Risi S, Marco EJ, Hendren RL, Bearden CE, Rauen KA, Weiss LA. PMID: 24101678; PMCID: PMC4230531.
      View in: PubMed   Mentions: 69     Fields:    Translation:HumansCells
    49. Abnormal white matter microstructure in children with sensory processing disorders. Neuroimage Clin. 2013; 2:844-53. Owen JP, Marco EJ, Desai S, Fourie E, Harris J, Hill SS, Arnett AB, Mukherjee P. PMID: 24179836; PMCID: PMC3778265.
      View in: PubMed   Mentions: 70     Fields:    
    50. Autism traits in individuals with agenesis of the corpus callosum. J Autism Dev Disord. 2013 May; 43(5):1106-18. Lau YC, Hinkley LB, Bukshpun P, Strominger ZA, Wakahiro ML, Baron-Cohen S, Allison C, Auyeung B, Jeremy RJ, Nagarajan SS, Sherr EH, Marco EJ. PMID: 23054201; PMCID: PMC3625480.
      View in: PubMed   Mentions: 34     Fields:    Translation:Humans
    51. Children with autism show reduced somatosensory response: an MEG study. Autism Res. 2012 Oct; 5(5):340-51. Marco EJ, Khatibi K, Hill SS, Siegel B, Arroyo MS, Dowling AF, Neuhaus JM, Sherr EH, Hinkley LN, Nagarajan SS. PMID: 22933354; PMCID: PMC3474892.
      View in: PubMed   Mentions: 42     Fields:    Translation:Humans
    52. The role of corpus callosum development in functional connectivity and cognitive processing. PLoS One. 2012; 7(8):e39804. Hinkley LB, Marco EJ, Findlay AM, Honma S, Jeremy RJ, Strominger Z, Bukshpun P, Wakahiro M, Brown WS, Paul LK, Barkovich AJ, Mukherjee P, Nagarajan SS, Sherr EH. PMID: 22870191; PMCID: PMC3411722.
      View in: PubMed   Mentions: 66     Fields:    Translation:HumansCTClinical Trials
    53. Processing speed delays contribute to executive function deficits in individuals with agenesis of the corpus callosum. J Int Neuropsychol Soc. 2012 May; 18(3):521-9. Marco EJ, Harrell KM, Brown WS, Hill SS, Jeremy RJ, Kramer JH, Sherr EH, Paul LK. PMID: 22390821; PMCID: PMC3605885.
      View in: PubMed   Mentions: 28     Fields:    Translation:Humans
    54. Sensory processing in autism: a review of neurophysiologic findings. Pediatr Res. 2011 May; 69(5 Pt 2):48R-54R. Marco EJ, Hinkley LB, Hill SS, Nagarajan SS. PMID: 21289533; PMCID: PMC3086654.
      View in: PubMed   Mentions: 325     Fields:    Translation:Humans
    55. Acute necrotizing encephalopathy in 3 brothers. Pediatrics. 2010 Mar; 125(3):e693-8. Marco EJ, Anderson JE, Neilson DE, Strober JB. PMID: 20142283; PMCID: PMC3207236.
      View in: PubMed   Mentions: 18     Fields:    Translation:Humans
    56. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2. Am J Hum Genet. 2009 Jan; 84(1):44-51. Neilson DE, Adams MD, Orr CM, Schelling DK, Eiben RM, Kerr DS, Anderson J, Bassuk AG, Bye AM, Childs AM, Clarke A, Crow YJ, Di Rocco M, Dohna-Schwake C, Dueckers G, Fasano AE, Gika AD, Gionnis D, Gorman MP, Grattan-Smith PJ, Hackenberg A, Kuster A, Lentschig MG, Lopez-Laso E, Marco EJ, Mastroyianni S, Perrier J, Schmitt-Mechelke T, Servidei S, Skardoutsou A, Uldall P, van der Knaap MS, Goglin KC, Tefft DL, Aubin C, de Jager P, Hafler D, Warman ML. PMID: 19118815; PMCID: PMC2668029.
      View in: PubMed   Mentions: 111     Fields:    Translation:HumansCells
    57. Congenital lymphocytic choriomeningitis virus infection: spectrum of disease. Ann Neurol. 2007 Oct; 62(4):347-55. Bonthius DJ, Wright R, Tseng B, Barton L, Marco E, Karacay B, Larsen PD. PMID: 17557350.
      View in: PubMed   Mentions: 29     Fields:    Translation:Humans
    58. CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. Am J Hum Genet. 2007 Jul; 81(1):104-13. Brancati F, Barrano G, Silhavy JL, Marsh SE, Travaglini L, Bielas SL, Amorini M, Zablocka D, Kayserili H, Al-Gazali L, Bertini E, Boltshauser E, D'Hooghe M, Fazzi E, Fenerci EY, Hennekam RC, Kiss A, Lees MM, Marco E, Phadke SR, Rigoli L, Romano S, Salpietro CD, Sherr EH, Signorini S, Stromme P, Stuart B, Sztriha L, Viskochil DH, Yuksel A, Dallapiccola B, International JSRD Study Group, Valente EM, Gleeson JG. PMID: 17564967; PMCID: PMC1950920.
      View in: PubMed   Mentions: 70     Fields:    Translation:Humans
    59. Autism-lessons from the X chromosome. Soc Cogn Affect Neurosci. 2006 Dec; 1(3):183-93. Marco EJ, Skuse DH. PMID: 18985105; PMCID: PMC2555419.
      View in: PubMed   Mentions: 34     Fields:    Translation:HumansCells
    60. Case report: Y;6 translocation with deletion of 6p. Clin Dysmorphol. 2005 Apr; 14(2):93-96. Klein OD, Backstrand K, Cotter PD, Marco E, Sherr E, Slavotinek A. PMID: 15770132.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    61. Infant botulism, type F, presenting at 54 hours of life. Pediatr Neurol. 2005 Mar; 32(3):193-6. Keet CA, Fox CK, Margeta M, Marco E, Shane AL, Dearmond SJ, Strober JB, Miller SP. PMID: 15730901.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    62. Incomplete Brown-Séquard syndrome after methamphetamine injection into the neck. Neurology. 2003 Jun 24; 60(12):2015-6. Hwang W, Ralph J, Marco E, Hemphill JC. PMID: 12821761.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    63. Predictive model for pain recurrence after posterior fossa surgery for trigeminal neuralgia. Arch Neurol. 2002 Aug; 59(8):1297-302. Theodosopoulos PV, Marco E, Applebury C, Lamborn KR, Wilson CB. PMID: 12164727.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    64. Double-blind antiglucocorticoid treatment in schizophrenia and schizoaffective disorder: a pilot study. World J Biol Psychiatry. 2002 Jul; 3(3):156-61. Marco EJ, Wolkowitz OM, Vinogradov S, Poole JH, Lichtmacher J, Reus VI. PMID: 12478881.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCTClinical Trials
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