InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
Houston, TX 77030
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    Other Positions
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neurology

    InstitutionBaylor College of Medicine
    DepartmentDepartment of Neuroscience

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    K08NS001433     (CLARK, GARY D)Feb 1, 1991 - Jan 31, 1996
    Role: Principal Investigator

    R29NS037146     (CLARK, GARY D)Dec 1, 1997 - Nov 30, 2002
    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.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    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. 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 Jul 22; 1-7. PMID: 35901680.
      Citations:    Fields:    
    2. 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
    3. 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
    4. 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:    
    5. Clark GD, Lotze TE. Neurology in a Pandemic. Neurol Clin. 2021 08; 39(3):699-704. PMID: 34215381.
      Citations: 1     Fields:    Translation:Humans
    6. 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
    7. 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
    8. Cope H, Spillmann R, Rosenfeld JA, Brokamp E, Signer R, Schoch K, Kelley EG, Sullivan JA, Macnamara E, Lincoln S, Golden-Grant K, Orengo JP, Clark G, Burrage LC, Posey JE, Punetha J, Robertson A, Cogan J, Phillips JA, Martinez-Agosto J, Shashi V. 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.
      Citations: 4     Fields:    Translation:Humans
    9. Zawerton A, Mignot C, Sigafoos A, Blackburn PR, Haseeb A, McWalter K, Ichikawa S, 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, Guillen Sacoto MJ, Schnur RE, Zhu Z, Poisson A, El Chehadeh S, Alembik Y, Bruel AL, Lehalle D, Nambot S, Moutton S, Odent S, Jaillard S, Dubourg C, 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, Hoffer MJV, Vargas M, Wojcik A, Cherik F, Francannet C, 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, Nizon M, Cogné B, Kuechler A, Piton A, Klee EW, Lefebvre V, Clark KJ, 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.
      Citations: 4     Fields:    Translation:HumansAnimals
    10. 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
    11. 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
    12. Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Martínez-Agosto JA, 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, Yamamoto S, Wangler MF, Mirzaa G, Hemelsoet D, Lee B, Nelson SF, Goldstein DB, Bellen HJ, Pena LDM. IRF2BPL Is Associated with Neurological Phenotypes. Am J Hum Genet. 2018 08 02; 103(2):245-260. PMID: 30057031.
      Citations: 25     Fields:    
    13. 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
    14. 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. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative. Genet Med. 2019 01; 21(1):161-172. PMID: 29907797.
      Citations: 26     Fields:    Translation:Humans
    15. 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
    16. Oláhová M, 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, Contrepois K, Zappala Z, Frésard L, Waggott D, Zink EM, Kim YM, Heyman HM, Stratton KG, Webb-Robertson BM, Snyder M, Merker JD, Montgomery SB, Fisher PG, Feichtinger RG, 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. 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.
      Citations: 33     Fields:    Translation:HumansCells
    17. 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, 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.
      Citations: 17     Fields:    Translation:Humans
    18. 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.
      Citations: 2     
    19. 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
    20. Wang J, Al-Ouran R, Hu Y, Kim SY, Wan YW, Wangler MF, Yamamoto S, Chao HT, Comjean A, Mohr SE, 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.
      Citations: 82     Fields:    Translation:Humans
    21. Spillmann RC, McConkie-Rosell A, Pena L, Jiang YH, Schoch K, Walley N, Sanders C, Sullivan J, Hooper SR, Shashi V. 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.
      Citations: 18     Fields:    Translation:Humans
    22. 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, 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.
      Citations: 50     Fields:    Translation:HumansCells
    23. Shashi V, Pena LD, Kim K, Burton B, Hempel M, Schoch K, Walkiewicz M, McLaughlin HM, Cho M, Stong N, Hickey SE, Shuss CM, 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, Petrovski S, Kuismin O, Korpi-Heikkilä S, Pietilainen O, Aarno P, Kurki MI, Hoischen A, Need AC, Goldstein DB, Kortüm 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.
      Citations: 27     Fields:    Translation:Humans
    24. 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
    25. 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.
      Citations: 35     Fields:    Translation:HumansCells
    26. Clark GD. Platelet-Activating Factor Acetylhydrolase and Brain Development. Enzymes. 2015; 38:37-42. PMID: 26612645.
      Citations: 5     Fields:    
    27. 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.
      Citations: 24     Fields:    Translation:HumansCells
    28. 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.
      Citations: 8     Fields:    Translation:Humans
    29. 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.
      Citations: 1     Fields:    Translation:Humans
    30. 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
    31. 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.
      Citations: 213     Fields:    Translation:HumansCells
    32. 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.
      Citations: 10     Fields:    Translation:AnimalsCells
    33. 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.
      Citations: 26     Fields:    Translation:Humans
    34. 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.
      Citations: 27     Fields:    Translation:HumansCells
    35. 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.
      Citations: 6     Fields:    Translation:Animals
    36. 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
    37. 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.
      Citations: 27     Fields:    Translation:HumansAnimalsCells
    38. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM. 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
    39. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM. Reporting recommendations for tumor marker prognostic studies. J Clin Oncol. 2005 Dec 20; 23(36):9067-72. PMID: 16172462.
      Citations: 315     Fields:    Translation:Humans
    40. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM. 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
    41. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM. 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
    42. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM. 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
    43. McShane LM, Altman DG, Sauerbrei W, Taube SE, Gion M, Clark GM. REporting recommendations for tumour MARKer prognostic studies (REMARK). Eur J Cancer. 2005 Aug; 41(12):1690-6. PMID: 16043346.
      Citations: 116     Fields:    Translation:Humans
    44. 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
    45. 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
    46. 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: 82     Fields:    Translation:HumansAnimalsCells
    47. 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.
      Citations: 33     Fields:    Translation:Animals
    48. 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: 14     Fields:    Translation:Humans
    49. 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
    50. 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
    51. 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.
      Citations: 32     Fields:    Translation:AnimalsCells
    52. Clark GD. Cerebral gyral dysplasias: molecular genetics and cell biology. Curr Opin Neurol. 2001 Apr; 14(2):157-62. PMID: 11262729.
      Citations: 3     Fields:    Translation:HumansAnimals
    53. 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: 4     Fields:    Translation:AnimalsCells
    54. 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: 7     Fields:    Translation:HumansCells
    55. 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
    56. 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
    57. 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: 204     Fields:    Translation:AnimalsCells
    58. 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
    59. 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.
      Citations: 31     Fields:    Translation:AnimalsCells
    60. 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
    61. 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: 7     Fields:    Translation:HumansCells
    62. 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
    63. 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: 7     Fields:    Translation:AnimalsCells
    64. 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: 46     Fields:    Translation:Animals
    65. 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: 8     Fields:    Translation:AnimalsCells
    66. 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: 4     Fields:    Translation:AnimalsCells
    67. 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: 34     Fields:    Translation:AnimalsCells
    68. 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
    69. 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: 28     Fields:    Translation:AnimalsCells
    70. 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
    71. 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
    72. 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
    73. 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: 12     Fields:    Translation:Animals
    74. 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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