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GARY CLARK

TitleProfessor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
ORCID ORCID Icon0000-0002-6304-7469 Additional info
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    Other Positions
    TitleProfessor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neurology
    DivisionNeurology

    TitleProfessor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neuroscience
    DivisionNeuroscience


    Collapse Research 
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    R29NS037146     (CLARK, GARY D)Dec 1, 1997 - Nov 30, 2002
    NIH
    SYNAPTIC PLASTICITY IN HIPPOCAMPAL EPILEPTOGENESIS
    Role: Principal Investigator
    K08NS001433     (CLARK, GARY D)Feb 1, 1991 - Jan 31, 1996
    NIH
    CALCIUM DEPENDENT REGULATION OF NMDA CURRENTS
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    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. Weinstock A, Bebin EM, Checketts D, Clark GD, Szaflarski JP, Seltzer LE, Thiele EA, Sahebkar F. Long-term efficacy and safety of cannabidiol in patients with tuberous sclerosis complex: 3-year results from the cannabidiol expanded access program. Epilepsia Open. 2024 Oct; 9(5):1816-1825. PMID: 39088193; PMCID: PMC11450615.
      Citations: 1     Fields:    Translation:Humans
    2. Li S, Zhao S, Sinson JC, Bajic A, Rosenfeld JA, Neeley MB, Pena M, Worley KC, Burrage LC, Weisz-Hubshman M, Ketkar S, Craigen WJ, Clark GD, Lalani S, Bacino CA, Machol K, Chao HT, Potocki L, Emrick L, Sheppard J, Nguyen MTT, Khoramnia A, Hernandez PP, Nagamani SC, Liu Z, Undiagnosed Diseases Network, Eng CM, Lee B, Liu P. The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing. Am J Hum Genet. 2024 05 02; 111(5):841-862. PMID: 38593811; PMCID: PMC11080285.
      Citations: 1     Fields:    Translation:HumansCells
    3. Pucel J, Briere LC, Reuter C, Gochyyev P, Undiagnosed Diseases Network, LeBlanc K. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis. Genet Med. 2024 06; 26(6):101115. PMID: 38436216; PMCID: PMC11161308.
      Citations:    Fields:    Translation:Humans
    4. Flamini RJ, Comi AM, Bebin EM, Chez MG, Clark G, Devinsky O, Hussain SA, Lyons PD, Patel AD, Rosengard JL, Sahebkar F, Segal E, Seltzer L, Szaflarski JP, Weinstock A. Efficacy of cannabidiol in convulsive and nonconvulsive seizure types associated with treatment-resistant epilepsies in the Expanded Access Program. Epilepsia. 2023 08; 64(8):e156-e163. PMID: 37243404.
      Citations: 1     Fields:    Translation:Humans
    5. Halley MC, Young JL, Tang C, Mintz KT, Lucas-Griffin S, Maghiro A, Ashley EA, Tabor HK, Undiagnosed Diseases Network. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care. J Pediatr. 2023 10; 261:113537. PMID: 37271495; PMCID: PMC10527480.
      Citations:    
    6. Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, G??wein S, Di Donato N, Bertini ES, Undiagnosed Diseases Network, Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Bi-allelic variants in INTS11 are associated with a complex neurological disorder. Am J Hum Genet. 2023 05 04; 110(5):774-789. PMID: 37054711; PMCID: PMC10183469.
      Citations: 2     Fields:    Translation:HumansAnimals
    7. Rosenfeld LE, LeBlanc K, Nagy A, Ego BK, Undiagnosed Diseases Network, McCray AT. Participation in a national diagnostic research study: assessing the patient experience. Orphanet J Rare Dis. 2023 04 10; 18(1):73. PMID: 37032333; PMCID: PMC10084693.
      Citations:    
    8. Akula SK, Marciano JH, Lim Y, Exposito-Alonso D, Hylton NK, Hwang GH, Neil JE, Dominado N, Bunton-Stasyshyn RK, Song JHT, Talukdar M, Schmid A, Teboul L, Mo A, Shin T, Finander B, Beck SG, Yeh RC, Otani A, Qian X, DeGennaro EM, Alkuraya FS, Maddirevula S, Cascino GD, Giannini C, Undiagnosed Diseases Network, Burrage LC, Rosenfield JA, Ketkar S, Clark GD, Bacino C, Lewis RA, Segal RA, Bazan JF, Smith KA, Golden JA, Cho G, Walsh CA. TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system. Proc Natl Acad Sci U S A. 2023 Jan 24; 120(4):e2209964120. PMID: 36669111; PMCID: PMC9942790.
      Citations: 4     Fields:    Translation:HumansAnimalsCells
    9. Chong SC, Cao Y, Fung ELW, Kleppe S, Gripp KW, Hertecant J, El-Hattab AW, Suleiman J, Clark G, von Allmen G, Rodziyevska O, Lewis RA, Rosenfeld JA, Dong J, Undiagnosed Diseases Network, Wang X, Miller MJ, Bi W, Liu P, Scaglia F. Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. Am J Med Genet A. 2023 03; 191(3):776-785. PMID: 36537114.
      Citations: 1     Fields:    Translation:Humans
    10. Gadgil N, McClugage SG, Aldave G, Bauer DF, Weiner HL, Huisman TAGM, Sanz-Cortes M, Belfort MA, Emrick L, Clark G, Joyeux L, Whitehead WE. Natural history of posterior fetal cephaloceles and incidence of progressive cephalocele herniation. J Neurosurg Pediatr. 2022 Sep 01; 30(3):342-348. PMID: 35901680.
      Citations:    Fields:    
    11. Clark GD, Lotze TE. Neurology in a Pandemic. Neurol Clin. 2021 08; 39(3):699-704. PMID: 34215381.
      Citations: 1     Fields:    Translation:Humans
    12. Clark GD, Lotze TE. Novel Treatments and Clinical Research in Child Neurology. Neurol Clin. 2021 08; 39(3):719-722. PMID: 34215383.
      Citations:    Fields:    Translation:Humans
    13. Clark GD, Riviello JJ. Memento Akademia: Introduction and Editorial Regarding the State of Child Neurology. Neurol Clin. 2021 08; 39(3):xiii-xv. PMID: 34215393.
      Citations:    Fields:    
    14. LaRose M, Cordasco BD, DiPrisco D, Clark GD. The Finances of Neurology in a Major Children's Hospital. Neurol Clin. 2021 08; 39(3):689-697. PMID: 34215380.
      Citations:    Fields:    Translation:Humans
    15. Herman I, Karakas C, Webber TA, Kralik SF, Takacs DS, Fisher KS, Edmondson EA, Riviello JJ, Clark GD, Pehlivan D. Clinical Profile and Long-Term Outcome in Neonatal Cerebral Sinus Venous Thrombosis. Pediatr Neurol. 2021 08; 121:20-25. PMID: 34126318.
      Citations:    Fields:    Translation:Humans
    16. Mitre V, Heym K, Clark GD, Venkatramani R. Neurocutaneous Melanocytosis and Leptomeningeal Melanoma. J Pediatr Hematol Oncol. 2021 03 01; 43(2):e195-e197. PMID: 31764519.
      Citations: 3     Fields:    Translation:Humans
    17. Thiele EA, Bebin EM, Jansen FE, Kotulska K, Lawson JA, O'Callaghan FJ, Wong M, Sahebkar F, Checketts D, Knappertz V, GWPCARE6 Study Group, Bhathal H. Add-on Cannabidiol Treatment for Drug-Resistant Seizures in Tuberous Sclerosis Complex: A Placebo-Controlled Randomized Clinical Trial. JAMA Neurol. 2021 03 01; 78(3):285-292. PMID: 33346789; PMCID: PMC7754080.
      Citations:    
    18. Cope H, Spillmann R, Rosenfeld JA, Brokamp E, Signer R, Schoch K, Kelley EG, Sullivan JA, Macnamara E, Lincoln S, Golden-Grant K, Undiagnosed Diseases Network, Orengo JP, Clark G, Burrage LC, Posey JE, Punetha J, Robertson A, Cogan J, Phillips JA, Martinez-Agosto J, Shashi V, Glanton E. Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network. Mol Genet Genomic Med. 2020 10; 8(10):e1397. PMID: 32730690; PMCID: PMC7549585.
      Citations: 4     Fields:    Translation:Humans
    19. Zawerton A, Sigafoos A, Blackburn PR, Haseeb A, McWalter K, Ichikawa S, Guillen Sacoto MJ, Schnur RE, Zhu Z, Hilhorst-Hofstee Y, Barbaro-Dieber T, Ortega L, Bhoj EJ, Masser-Frye D, Bird LM, Lindstrom K, Ramsey KM, Narayanan V, Fassi E, Willing M, Cole T, Salter CG, Akilapa R, Vandersteen A, Canham N, Rump P, Gerkes EH, Klein Wassink-Ruiter JS, Bijlsma E, Vargas M, Wojcik A, Rosenfeld JA, Machol K, Scott DA, Bacino CA, Wang X, Clark GD, Bertoli M, Zwolinski S, Thomas RH, Akay E, Chang RC, Bressi R, Sanchez Russo R, Srour M, Russell L, Goyette AE, Dupuis L, Mendoza-Londono R, Karimov C, Joseph M, Deciphering Developmental Disorder Study, Klee EW, Clark KJ, Mignot C, Nava C, Keren B, Charles P, Marey I, Tabet AC, Levy J, Perrin L, Hartmann A, Lesca G, Schluth-Bolard C, Monin P, Dupuis-Girod S, Poisson A, El Chehadeh S, Alembik Y, Bruel AL, Lehalle D, Nambot S, Moutton S, Odent S, Jaillard S, Dubourg C, Hoffer MJV, Cherik F, Francannet C, Nizon M, Cogn? B, Kuechler A, Piton A, Lefebvre V, Depienne C. Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency. Genet Med. 2020 03; 22(3):524-537. PMID: 31578471; PMCID: PMC9063678.
      Citations: 4     Fields:    Translation:HumansAnimals
    20. Whiting SE, Carson AM, Clark GD, Schwartz DD. Case report of prenatal bilateral cerebellar infarction: implications for social-behavioral functioning. Clin Neuropsychol. 2019 07; 33(5):890-904. PMID: 30698067.
      Citations: 1     Fields:    Translation:Humans
    21. Lyons-Warren AM, Risen SR, Clark G. Infant Botulism With Asymmetric Cranial Nerve Palsies. Pediatr Neurol. 2019 03; 92:71-72. PMID: 30639248.
      Citations:    Fields:    Translation:Humans
    22. Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Herzog M, Chen AH, Dickson PI, Lin HJ, Vera MU, Salamon N, Graham JM, Ortiz D, Infante E, Steyaert W, Dermaut B, Poppe B, Chung HL, Zuo Z, Lee PT, Kanca O, Xia F, Yang Y, Smith EC, Jasien J, Kansagra S, Spiridigliozzi G, El-Dairi M, Lark R, Riley K, Koeberl DD, Golden-Grant K, Program for Undiagnosed Diseases (UD-PrOZA), Undiagnosed Diseases Network, Yamamoto S, Wangler MF, Mirzaa G, Hemelsoet D, Lee B, Nelson SF, Goldstein DB, Bellen HJ, Pena LDM, Mart?nez-Agosto JA. IRF2BPL Is Associated with Neurological Phenotypes. Am J Hum Genet. 2018 08 02; 103(2):245-260. PMID: 30057031; PMCID: PMC6081494.
      Citations: 25     Fields:    
    23. Devinsky O, Verducci C, Thiele EA, Laux LC, Patel AD, Filloux F, Szaflarski JP, Wilfong A, Clark GD, Park YD, Seltzer LE, Bebin EM, Flamini R, Wechsler RT, Friedman D. Open-label use of highly purified CBD (Epidiolex?) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes. Epilepsy Behav. 2018 09; 86:131-137. PMID: 30006259.
      Citations: 37     Fields:    Translation:HumansCells
    24. Shashi V, Schoch K, Spillmann R, Cope H, Tan QK, Walley N, Pena L, McConkie-Rosell A, Jiang YH, Stong N, Need AC, Goldstein DB, Undiagnosed Diseases Network. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative. Genet Med. 2019 01; 21(1):161-172. PMID: 29907797; PMCID: PMC6295275.
      Citations: 26     Fields:    Translation:Humans
    25. Stowe RC, Jimenez-Gomez A, Balasa A, Clark GD. Cockayne Syndrome Complicated by Moyamoya Vasculopathy and Stroke. Pediatr Neurol. 2018 09; 86:73-74. PMID: 30089552.
      Citations: 1     Fields:    Translation:Humans
    26. GWPCARE3 Study Group, Devinsky O, Patel AD, Cross JH, Villanueva V, Wirrell EC, Privitera M, Greenwood SM, Roberts C, Checketts D, VanLandingham KE, Zuberi SM. Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut Syndrome. N Engl J Med. 2018 May 17; 378(20):1888-1897. PMID: 29768152.
      Citations:    
    27. Yoon WH, Thompson K, Jangam S, Fernandez L, Davidson JM, Kyle JE, Grove ME, Fisk DG, Kohler JN, Holmes M, Dries AM, Huang Y, Zhao C, Zappala Z, Waggott D, Zink EM, Kim YM, Heyman HM, Stratton KG, Webb-Robertson BM, Undiagnosed Diseases Network, Snyder M, Merker JD, Montgomery SB, Fisher PG, Mayr JA, Hall J, Barbosa IA, Simpson MA, Deshpande C, Waters KM, Koeller DM, Metz TO, Morris AA, Schelley S, Cowan T, Friederich MW, McFarland R, Van Hove JLK, Enns GM, Yamamoto S, Ashley EA, Wangler MF, Taylor RW, Bellen HJ, Bernstein JA, Wheeler MT, Ol?hov? M, Contrepois K, Fr?sard L, Feichtinger RG. Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. Am J Hum Genet. 2018 03 01; 102(3):494-504. PMID: 29478781; PMCID: PMC6117612.
      Citations: 33     Fields:    Translation:HumansCells
    28. Pena LDM, Jiang YH, Schoch K, Spillmann RC, Walley N, Stong N, Rapisardo Horn S, Sullivan JA, McConkie-Rosell A, Kansagra S, Smith EC, El-Dairi M, Bellet J, Keels MA, Jasien J, Kranz PG, Noel R, Nagaraj SK, Lark RK, Wechsler DSG, Del Gaudio D, Leung ML, Hendon LG, Parker CC, Jones KL, Undiagnosed Diseases Network Members, Goldstein DB, Shashi V. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases. Genet Med. 2018 04; 20(4):464-469. PMID: 28914269; PMCID: PMC5851806.
      Citations: 17     Fields:    Translation:Humans
    29. Messinger MM, Misra SN, Clark GD, DiCarlo SM. Evaluation of Safety in Exceeding Maximum Adult Doses of Commonly Used Second-Generation Antiepileptic Drugs in Pediatric Patients. J Pediatr Pharmacol Ther. 2017 Jul-Aug; 22(4):256-260. PMID: 28943819; PMCID: PMC5562204.
      Citations: 2     
    30. Cannabidiol in Dravet Syndrome Study Group, Devinsky O, Cross JH, Laux L, Marsh E, Miller I, Nabbout R, Scheffer IE, Thiele EA, Wright S. Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome. N Engl J Med. 2017 05 25; 376(21):2011-2020. PMID: 28538134.
      Citations: 342     Fields:    Translation:Humans
    31. Wang J, Al-Ouran R, Hu Y, Kim SY, Wan YW, Wangler MF, Yamamoto S, Chao HT, Comjean A, Mohr SE, UDN, Perrimon N, Liu Z, Bellen HJ. MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome. Am J Hum Genet. 2017 Jun 01; 100(6):843-853. PMID: 28502612; PMCID: PMC5670038.
      Citations: 82     Fields:    Translation:Humans
    32. Spillmann RC, McConkie-Rosell A, Pena L, Jiang YH, Undiagnosed Diseases Network, Schoch K, Walley N, Sanders C, Sullivan J, Shashi V, Hooper SR. A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network. Orphanet J Rare Dis. 2017 04 17; 12(1):71. PMID: 28416019; PMCID: PMC5392939.
      Citations: 18     Fields:    Translation:Humans
    33. Chao HT, Davids M, Burke E, Pappas JG, Rosenfeld JA, McCarty AJ, Davis T, Wolfe L, Toro C, Tifft C, Xia F, Stong N, Johnson TK, Warr CG, Undiagnosed Diseases Network, Yamamoto S, Adams DR, Markello TC, Gahl WA, Bellen HJ, Wangler MF, Malicdan MCV. A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3. Am J Hum Genet. 2017 Jan 05; 100(1):128-137. PMID: 28017372; PMCID: PMC5223093.
      Citations: 50     Fields:    Translation:HumansCells
    34. Shashi V, Pena LD, Kim K, Burton B, Hempel M, Schoch K, Walkiewicz M, McLaughlin HM, Cho M, Stong N, Hickey SE, Shuss CM, Undiagnosed Diseases Network, Freemark MS, Bellet JS, Keels MA, Bonner MJ, El-Dairi M, Butler M, Kranz PG, Stumpel CT, Klinkenberg S, Oberndorff K, Alawi M, Santer R, Kuismin O, Pietilainen O, Aarno P, Kurki MI, Hoischen A, Need AC, Goldstein DB, Petrovski S, Korpi-Heikkil? S, Kort?m F. De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype. Am J Hum Genet. 2016 Oct 06; 99(4):991-999. PMID: 27693232; PMCID: PMC5065681.
      Citations: 27     Fields:    Translation:Humans
    35. Thorning H, Marino L, Jean-Noel P, Lopez L, Covell NH, Chiang IC, Myers RW, Ruderman DP, Haggerty NK, Clark G, Dixon LB. Adoption of a Blended Training Curriculum for ACT in New York State. Psychiatr Serv. 2016 09 01; 67(9):940-2. PMID: 27181739.
      Citations:    
    36. Ziats MN, Goin-Kochel RP, Berry LN, Ali M, Ge J, Guffey D, Rosenfeld JA, Bader P, Gambello MJ, Wolf V, Penney LS, Miller R, Lebel RR, Kane J, Bachman K, Troxell R, Clark G, Minard CG, Stankiewicz P, Beaudet A, Schaaf CP. The complex behavioral phenotype of 15q13.3 microdeletion syndrome. Genet Med. 2016 11; 18(11):1111-1118. PMID: 26963284.
      Citations: 22     Fields:    Translation:HumansCells
    37. Lalani SR, Liu P, Rosenfeld JA, Watkin LB, Chiang T, Leduc MS, Zhu W, Ding Y, Pan S, Vetrini F, Miyake CY, Shinawi M, Gambin T, Eldomery MK, Akdemir ZH, Emrick L, Wilnai Y, Schelley S, Koenig MK, Memon N, Farach LS, Coe BP, Azamian M, Hernandez P, Zapata G, Jhangiani SN, Muzny DM, Lotze T, Clark G, Wilfong A, Northrup H, Adesina A, Bacino CA, Scaglia F, Bonnen PE, Crosson J, Duis J, Maegawa GH, Coman D, Inwood A, McGill J, Boerwinkle E, Graham B, Beaudet A, Eng CM, Hanchard NA, Xia F, Orange JS, Gibbs RA, Lupski JR, Yang Y. Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations. Am J Hum Genet. 2016 Feb 04; 98(2):347-57. PMID: 26805781; PMCID: PMC4746334.
      Citations: 35     Fields:    Translation:HumansCells
    38. Clark GD. Platelet-Activating Factor Acetylhydrolase and Brain Development. Enzymes. 2015; 38:37-42. PMID: 26612645.
      Citations: 5     Fields:    
    39. Bernier UR, Gurman P, Clark GG, Elman N. Functional Micro-Dispensers based on Micro-Electro-Mechanical-Systems (MEMS) integrated with fabrics as functional materials to protect humans from mosquito feeding. J Control Release. 2015 Dec 28; 220(Pt A):1-4. PMID: 26415856.
      Citations:    
    40. Clark GG, Fern?ndez-Salas I. Mosquito vector biology and control in latin america-a 24th symposium. J Am Mosq Control Assoc. 2014 Sep; 30(3):204-14. PMID: 25843096.
      Citations:    
    41. Clark GG, Fernandez-Salas I. Mosquito vector biology and control in Latin America--a 23rd symposium. J Am Mosq Control Assoc. 2013 Sep; 29(3):251-69. PMID: 24199500.
      Citations:    
    42. Clark GG, Rubio-Palis Y. Mosquito vector biology and control in Latin America--a 22nd symposium. J Am Mosq Control Assoc. 2012 Jun; 28(2):102-10. PMID: 22894120.
      Citations:    
    43. Murdock DR, Clark GD, Bainbridge MN, Newsham I, Wu YQ, Muzny DM, Cheung SW, Gibbs RA, Ramocki MB. Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria. Am J Med Genet A. 2011 Sep; 155A(9):2071-7. PMID: 21834044; PMCID: PMC3616765.
      Citations: 24     Fields:    Translation:HumansCells
    44. Ramocki MB, Scaglia F, Stankiewicz P, Belmont JW, Jones JY, Clark GD. Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2. Am J Med Genet A. 2011 Jul; 155A(7):1574-80. PMID: 21638761; PMCID: PMC3121908.
      Citations: 8     Fields:    Translation:Humans
    45. Ansari SA, Hunter JV, Nassif LM, Clark GD, Ramocki MB. Bilateral in utero cerebellar infarction. J Child Neurol. 2011 Jul; 26(7):895-9. PMID: 21266324; PMCID: PMC3128202.
      Citations: 1     Fields:    Translation:Humans
    46. Clark GG, Rubio-Palis Y. Mosquito vector biology and control in Latin America--a 20th symposium. J Am Mosq Control Assoc. 2010 Sep; 26(3):306-20. PMID: 21033058.
      Citations:    
    47. El-Hakam LM, Volpi J, Mawad M, Clark G. Angioplasty for acute stroke with pediatric moyamoya syndrome. J Child Neurol. 2010 Oct; 25(10):1278-83. PMID: 20505156.
      Citations: 3     Fields:    Translation:Humans
    48. Shinawi M, Liu P, Kang SH, Shen J, Belmont JW, Scott DA, Probst FJ, Craigen WJ, Graham BH, Pursley A, Clark G, Lee J, Proud M, Stocco A, Rodriguez DL, Kozel BA, Sparagana S, Roeder ER, McGrew SG, Kurczynski TW, Allison LJ, Amato S, Savage S, Patel A, Stankiewicz P, Beaudet AL, Cheung SW, Lupski JR. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size. J Med Genet. 2010 May; 47(5):332-41. PMID: 19914906; PMCID: PMC3158566.
      Citations: 213     Fields:    Translation:HumansCells
    49. Zhang G, Assadi AH, Roceri M, Clark GD, D'Arcangelo G. Differential interaction of the Pafah1b alpha subunits with the Reelin transducer Dab1. Brain Res. 2009 Apr 24; 1267:1-8. PMID: 19272360; PMCID: PMC2673792.
      Citations: 10     Fields:    Translation:AnimalsCells
    50. Hopkins B, Sutton VR, Lewis RA, Van den Veyver I, Clark G. Neuroimaging aspects of Aicardi syndrome. Am J Med Genet A. 2008 Nov 15; 146A(22):2871-8. PMID: 18925666; PMCID: PMC2597151.
      Citations: 26     Fields:    Translation:Humans
    51. Dobyns WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry CJ, McDonald-McGinn D, Medne L, Zackai E, Parsons J, Zand DJ, Hisama FM, Walsh CA, Leventer RJ, Martin CL, Gajecka M, Shaffer LG. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2. Am J Med Genet A. 2008 Jul 01; 146A(13):1637-54. PMID: 18536050; PMCID: PMC2801020.
      Citations: 27     Fields:    Translation:HumansCells
    52. Assadi AH, Zhang G, McNeil R, Clark GD, D'Arcangelo G. Pafah1b2 mutations suppress the development of hydrocephalus in compound Pafah1b1; Reln and Pafah1b1; Dab1 mutant mice. Neurosci Lett. 2008 Jul 04; 439(1):100-5. PMID: 18514414; PMCID: PMC2680094.
      Citations: 6     Fields:    Translation:Animals
    53. Bernier UR, Allan SA, Quinn BP, Kline DL, Barnard DR, Clark GG. Volatile compounds from the integument of White Leghorn Chickens (Gallus gallus domesticus L.): candidate attractants of ornithophilic mosquito species. J Sep Sci. 2008 Apr; 31(6-7):1092-9. PMID: 18381686.
      Citations:    
    54. Berg JS, Brunetti-Pierri N, Peters SU, Kang SH, Fong CT, Salamone J, Freedenberg D, Hannig VL, Prock LA, Miller DT, Raffalli P, Harris DJ, Erickson RP, Cunniff C, Clark GD, Blazo MA, Peiffer DA, Gunderson KL, Sahoo T, Patel A, Lupski JR, Beaudet AL, Cheung SW. Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region. Genet Med. 2007 Jul; 9(7):427-41. PMID: 17666889.
      Citations: 71     Fields:    Translation:HumansCells
    55. Zhang G, Assadi AH, McNeil RS, Beffert U, Wynshaw-Boris A, Herz J, Clark GD, D'Arcangelo G. The Pafah1b complex interacts with the reelin receptor VLDLR. PLoS One. 2007 Feb 28; 2(2):e252. PMID: 17330141; PMCID: PMC1800349.
      Citations: 27     Fields:    Translation:HumansAnimalsCells
    56. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM, Statistics Subcommittee of NCI-EORTC Working Group on Cancer Diagnostics. REporting recommendations for tumor MARKer prognostic studies (REMARK). Breast Cancer Res Treat. 2006 Nov; 100(2):229-35. PMID: 16932852.
      Citations: 296     Fields:    Translation:Humans
    57. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM, Statistics Subcommittee of the NCI-EORTC Working Group on Cancer Diagnostics. Reporting recommendations for tumor marker prognostic studies. J Clin Oncol. 2005 Dec 20; 23(36):9067-72. PMID: 16172462.
      Citations: 315     Fields:    Translation:Humans
    58. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM, Statistics Subcommittee of the NCI-EORTC Working Group on Cancer Diagnostics. Reporting recommendations for tumor marker prognostic studies (REMARK). J Natl Cancer Inst. 2005 Aug 17; 97(16):1180-4. PMID: 16106022.
      Citations: 569     Fields:    Translation:Humans
    59. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM, Statistics Subcommittee of the NCI-EORTC Working Group on Cancer Diagnostics. REporting recommendations for tumour MARKer prognostic studies (REMARK). Eur J Cancer. 2005 Aug; 41(12):1690-6. PMID: 16043346.
      Citations: 116     Fields:    Translation:Humans
    60. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM, Statistics Subcommittee of the NCI-EORTC Working Group on Cancer Diagnostics. REporting recommendations for tumor MARKer prognostic studies (REMARK). Nat Clin Pract Oncol. 2005 Aug; 2(8):416-22. PMID: 16130938.
      Citations: 112     Fields:    Translation:Humans
    61. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM, Statistics Subcommittee of the NCI-EORTC Working Group on Cancer Diagnostics. REporting recommendations for tumor MARKer prognostic studies (REMARK). Nat Clin Pract Urol. 2005 Aug; 2(8):416-22. PMID: 16482653.
      Citations: 90     Fields:    Translation:Humans
    62. Maricich SM, Neul JL, Lotze TE, Cazacu AC, Uyeki TM, Demmler GJ, Clark GD. Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas. Pediatrics. 2004 Nov; 114(5):e626-33. PMID: 15520093.
      Citations: 42     Fields:    Translation:HumansCells
    63. Clark GD. The classification of cortical dysplasias through molecular genetics. Brain Dev. 2004 Sep; 26(6):351-62. PMID: 15275695.
      Citations: 4     Fields:    Translation:Humans
    64. Chachoua A, Hammond LA, Rowinsky EK, Huberman M, Karp D, Rigas J, Clark GM, Bonomi P, P?rez-Soler R, Santab?rbara P. Determinants of tumor response and survival with erlotinib in patients with non--small-cell lung cancer. J Clin Oncol. 2004 Aug 15; 22(16):3238-47. PMID: 15310767.
      Citations: 250     Fields:    Translation:HumansCTClinical Trials
    65. Assadi AH, Zhang G, Beffert U, McNeil RS, Renfro AL, Niu S, Quattrocchi CC, Antalffy BA, Sheldon M, Armstrong DD, Wynshaw-Boris A, Herz J, D'Arcangelo G, Clark GD. Interaction of reelin signaling and Lis1 in brain development. Nat Genet. 2003 Nov; 35(3):270-6. PMID: 14578885.
      Citations: 87     Fields:    Translation:HumansAnimalsCells
    66. Yan W, Assadi AH, Wynshaw-Boris A, Eichele G, Matzuk MM, Clark GD. Previously uncharacterized roles of platelet-activating factor acetylhydrolase 1b complex in mouse spermatogenesis. Proc Natl Acad Sci U S A. 2003 Jun 10; 100(12):7189-94. PMID: 12775763; PMCID: PMC165851.
      Citations: 35     Fields:    Translation:Animals
    67. Sutton VR, O'Brien WE, Clark GD, Kim J, Wanders RJ. 3-Hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency. J Inherit Metab Dis. 2003; 26(1):69-71. PMID: 12872843.
      Citations: 16     Fields:    Translation:Humans
    68. Clark GD. Brain development and the genetics of brain development. Neurol Clin. 2002 Nov; 20(4):917-39. PMID: 12616675.
      Citations: 5     Fields:    Translation:HumansCells
    69. Poolos NP, Das S, Clark GD, Lardizabal D, Noebels JL, Wyllie E, Dobyns WB. Males with epilepsy, complete subcortical band heterotopia, and somatic mosaicism for DCX. Neurology. 2002 May 28; 58(10):1559-62. PMID: 12034802.
      Citations: 11     Fields:    Translation:Humans
    70. Aumais JP, Tunstead JR, McNeil RS, Schaar BT, McConnell SK, Lin SH, Clark GD, Yu-Lee LY. NudC associates with Lis1 and the dynein motor at the leading pole of neurons. J Neurosci. 2001 Dec 15; 21(24):RC187. PMID: 11734602; PMCID: PMC6763039.
      Citations: 35     Fields:    Translation:AnimalsCells
    71. Clark GD. Cerebral gyral dysplasias: molecular genetics and cell biology. Curr Opin Neurol. 2001 Apr; 14(2):157-62. PMID: 11262729.
      Citations: 5     Fields:    Translation:HumansAnimals
    72. Clark GD, Zorumski CF, McNeil RS, Happel LT, Ovella T, McGuire S, Bix GJ, Swann JW. Neuronal platelet-activating factor receptor signal transduction involves a pertussis toxin-sensitive G-protein. Neurochem Res. 2000 May; 25(5):603-11. PMID: 10905621.
      Citations: 3     Fields:    Translation:AnimalsCells
    73. Sweeney KJ, Clark GD, Prokscha A, Dobyns WB, Eichele G. Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development. Mech Dev. 2000 Apr; 92(2):263-71. PMID: 10727864.
      Citations: 9     Fields:    Translation:HumansCells
    74. Clark GD, Noebels JL. Cortin disaster: lissencephaly genes spell double trouble for the developing brain. Ann Neurol. 1999 Feb; 45(2):141-2. PMID: 9989613.
      Citations: 1     Fields:    Translation:Humans
    75. McNeil RS, Swann JW, Brinkley BR, Clark GD. Neuronal cytoskeletal alterations evoked by a platelet-activating factor (PAF) analogue. Cell Motil Cytoskeleton. 1999; 43(2):99-113. PMID: 10379835.
      Citations: 6     Fields:    Translation:AnimalsCells
    76. Hirotsune S, Fleck MW, Gambello MJ, Bix GJ, Chen A, Clark GD, Ledbetter DH, McBain CJ, Wynshaw-Boris A. Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat Genet. 1998 Aug; 19(4):333-9. PMID: 9697693.
      Citations: 215     Fields:    Translation:AnimalsCells
    77. Keller C, Shapira SK, Clark GD. A urea cycle defect presenting as acute cerebellar ataxia in a 3-year-old girl. J Child Neurol. 1998 Feb; 13(2):93-5. PMID: 9512312.
      Citations: 1     Fields:    Translation:Humans
    78. Bix GJ, Clark GD. Platelet-activating factor receptor stimulation disrupts neuronal migration In vitro. J Neurosci. 1998 Jan 01; 18(1):307-18. PMID: 9412509; PMCID: PMC6793386.
      Citations: 31     Fields:    Translation:AnimalsCells
    79. Bix GJ, Clark GD. Elvax as a slow-release delivery agent for a platelet-activating factor receptor agonist and antagonist. J Neurosci Methods. 1997 Nov 07; 77(1):67-74. PMID: 9402559.
      Citations: 2     Fields:    Translation:Animals
    80. Clark GD, Mizuguchi M, Antalffy B, Barnes J, Armstrong D. Predominant localization of the LIS family of gene products to Cajal-Retzius cells and ventricular neuroepithelium in the developing human cortex. J Neuropathol Exp Neurol. 1997 Sep; 56(9):1044-52. PMID: 9291945.
      Citations: 6     Fields:    Translation:HumansCells
    81. Clark GD, McNeil RS, Bix GJ, Swann JW. Platelet-activating factor produces neuronal growth cone collapse. Neuroreport. 1995 Dec 15; 6(18):2569-75. PMID: 8741765.
      Citations: 6     Fields:    Translation:AnimalsCells
    82. Clark GD, McNeil RS, Bix GJ, Swann JW. Lipids as axon guidance molecules? Neuroreport. 1995 Dec 15; 6(18):2446. PMID: 8741737.
      Citations:    Fields:    Translation:Cells
    83. Kato K, Clark GD, Bazan NG, Zorumski CF. Platelet-activating factor as a potential retrograde messenger in CA1 hippocampal long-term potentiation. Nature. 1994 Jan 13; 367(6459):175-9. PMID: 8114914.
      Citations: 44     Fields:    Translation:Animals
    84. Bazan NG, Zorumski CF, Clark GD. The activation of phospholipase A2 and release of arachidonic acid and other lipid mediators at the synapse: the role of platelet-activating factor. J Lipid Mediat. 1993 Mar-Apr; 6(1-3):421-7. PMID: 8395252.
      Citations: 9     Fields:    Translation:AnimalsCells
    85. Thio LL, Clark GD, Clifford DB, Zorumski CF. Wheat germ agglutinin enhances EPSCs in cultured postnatal rat hippocampal neurons by blocking ionotropic quisqualate receptor desensitization. J Neurophysiol. 1992 Dec; 68(6):1930-8. PMID: 1283405.
      Citations: 3     Fields:    Translation:AnimalsCells
    86. Clark GD, Happel LT, Zorumski CF, Bazan NG. Enhancement of hippocampal excitatory synaptic transmission by platelet-activating factor. Neuron. 1992 Dec; 9(6):1211-6. PMID: 1334422.
      Citations: 35     Fields:    Translation:AnimalsCells
    87. Zorumski CF, Thio LL, Clark GD, Clifford DB. Blockade of desensitization augments quisqualate excitotoxicity in hippocampal neurons. Neuron. 1990 Jul; 5(1):61-6. PMID: 2164404.
      Citations: 9     Fields:    Translation:AnimalsCells
    88. Clark GD, Clifford DB, Zorumski CF. The effect of agonist concentration, membrane voltage and calcium on N-methyl-D-aspartate receptor desensitization. Neuroscience. 1990; 39(3):787-97. PMID: 2151464.
      Citations: 29     Fields:    Translation:AnimalsCells
    89. Clark GD. Role of excitatory amino acids in brain injury caused by hypoxia-ischemia, status epilepticus, and hypoglycemia. Clin Perinatol. 1989 Jun; 16(2):459-74. PMID: 2545404.
      Citations: 3     Fields:    Translation:HumansAnimalsCells
    90. Zorumski CF, Thio LL, Clark GD, Clifford DB. Calcium influx through N-methyl-D-aspartate channels activates a potassium current in postnatal rat hippocampal neurons. Neurosci Lett. 1989 May 08; 99(3):293-9. PMID: 2542845.
      Citations: 13     Fields:    Translation:AnimalsCells
    91. Rothman SM, Thurston JH, Hauhart RE, Clark GD, Solomon JS. Ketamine protects hippocampal neurons from anoxia in vitro. Neuroscience. 1987 Jun; 21(3):673-8. PMID: 2819768.
      Citations: 13     Fields:    Translation:Animals
    92. Clark GD, Rothman SM. Blockade of excitatory amino acid receptors protects anoxic hippocampal slices. Neuroscience. 1987 Jun; 21(3):665-71. PMID: 2888040.
      Citations: 10     Fields:    Translation:AnimalsCells
    93. Clark GD, Key JD, Rutherford P, Bithoney WG. Munchausen's syndrome by proxy (child abuse) presenting as apparent autoerythrocyte sensitization syndrome: an unusual presentation of Polle syndrome. Pediatrics. 1984 Dec; 74(6):1100-2. PMID: 6504630.
      Citations: 3     Fields:    Translation:HumansCells
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