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1. McGinnis, RE; Fox, H; Yates, P; Cameron, LA; Barnes, MR; Gray, IC; Spurr, NK; Hurko, O; St Clair, D
   Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland
   NATURE GENETICS
   
   R.E. McGinnis et al., "Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland", NAT GENET, 28(2), 2001, pp. 128-129
2. Hurko, O
   Genetics and genomics in neuropsychopharmacology: the impact on drug discovery and development
   EUROPEAN NEUROPSYCHOPHARMACOLOGY
   
   O. Hurko, "Genetics and genomics in neuropsychopharmacology: the impact on drug discovery and development", EUR NEUROPS, 11(6), 2001, pp. 491-499
3. Elmaci, I; Ain, MC; Wright, MJ; Lee, RR; Sheppard, JME; Rigomonti, D; Hurko, O
   Perioperative intracranial hemorrhage in achondroplasia (vol 12, pg 217, 2000)
   JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY
   
   I. Elmaci et al., "Perioperative intracranial hemorrhage in achondroplasia (vol 12, pg 217, 2000)", J NEUROS AN, 13(1), 2001, pp. 59-59
4. Elmaci, I; Ain, MC; Wright, MJ; Lee, RR; Sheppard, JME; Rigamonti, D; Hurko, O
   Perioperative intracranial hemorrhage in achondroplasia - A case report
   JOURNAL OF NEUROSURGICAL ANESTHESIOLOGY
   
   I. Elmaci et al., "Perioperative intracranial hemorrhage in achondroplasia - A case report", J NEUROS AN, 12(3), 2000, pp. 217-220
5. Ain, MC; Elmaci, I; Hurko, O; Clatterbuck, RE; Lee, RR; Rigamonti, D
   Reoperation for spinal restenosis in achondroplasia
   JOURNAL OF SPINAL DISORDERS
   
   M.C. Ain et al., "Reoperation for spinal restenosis in achondroplasia", J SPINAL D, 13(2), 2000, pp. 168-173
6. Crockett, MM; Carten, MF; Hurko, O; Sponseller, PD
   Motor milestones in children with diastrophic dysplasia
   JOURNAL OF PEDIATRIC ORTHOPAEDICS
   
   M.M. Crockett et al., "Motor milestones in children with diastrophic dysplasia", J PED ORTH, 20(4), 2000, pp. 437-441
7. Hurko, O; Walsh, FS
   Novel drug development for amyotrophic lateral sclerosis
   JOURNAL OF THE NEUROLOGICAL SCIENCES
   
   O. Hurko e F.S. Walsh, "Novel drug development for amyotrophic lateral sclerosis", J NEUR SCI, 180(1-2), 2000, pp. 21-28
8. Crawford, TO; Sladky, JT; Hurko, O; Besner-Johnston, A; Kelley, RI
   Abnormal fatty acid metabolism in childhood spinal muscular atrophy
   ANNALS OF NEUROLOGY
   
   T.O. Crawford et al., "Abnormal fatty acid metabolism in childhood spinal muscular atrophy", ANN NEUROL, 45(3), 1999, pp. 337-343
9. Bellus, GA; Bamshad, MJ; Przylepa, KA; Dorst, J; Lee, RR; Hurko, O; Jabs, EW; Curry, CJR; Wilcox, WR; Lachman, RS; Rimoin, DL; Francomano, CA
   Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): Phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3
   AMERICAN JOURNAL OF MEDICAL GENETICS
   
   G.A. Bellus et al., "Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): Phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3", AM J MED G, 85(1), 1999, pp. 53-65
10. Becher, MW; Wills, ML; Noll, WM; Hurko, O; Price, DL
    Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion
    HUMAN PATHOLOGY
    
    M.W. Becher et al., "Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletion", HUMAN PATH, 30(5), 1999, pp. 577-581
11. Hurko, O; Provost, TT
    Neurology and the skin
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    
    O. Hurko e T.T. Provost, "Neurology and the skin", J NE NE PSY, 66(4), 1999, pp. 417-430
12. ZANFERRARI C; LAVADOS PM; HURKO O; OPPENHEIMER SM; WITYK RJ
    CEREBROVASCULAR DISEASES IN PATIENTS WITH MARFAN-SYNDROME - A RETROSPECTIVE STUDY
    Stroke
    
    C. Zanferrari et al., "CEREBROVASCULAR DISEASES IN PATIENTS WITH MARFAN-SYNDROME - A RETROSPECTIVE STUDY", Stroke, 29(1), 1998, pp. 71-71
13. MOGAYZEL PJ; CARROLL JL; LOUGHLIN GM; HURKO O; FRANCOMANO CA; MARCUS CL
    SLEEP-DISORDERED BREATHING IN CHILDREN WITH ACHONDROPLASIA
    The Journal of pediatrics
    
    P.J. Mogayzel et al., "SLEEP-DISORDERED BREATHING IN CHILDREN WITH ACHONDROPLASIA", The Journal of pediatrics, 132(4), 1998, pp. 667-671
14. HURKO O
    THE EXPLOSION OF NEUROGENETICS
    Current opinion in neurology
    
    O. Hurko, "THE EXPLOSION OF NEUROGENETICS", Current opinion in neurology, 10(2), 1997, pp. 77-83
15. HURKO O
    RECENT ADVANCES IN HERITABLE ATAXIAS
    Annals of neurology
    
    O. Hurko, "RECENT ADVANCES IN HERITABLE ATAXIAS", Annals of neurology, 41(1), 1997, pp. 4-6
16. POLYMEROPOULOS MH; HURKO O; HSU F; RUBENSTEIN J; BASNET S; LANE K; DIETZ H; SPETZLER RF; RIGAMONTI D
    LINKAGE OF THE LOCUS FOR CEREBRAL CAVERNOUS HEMANGIOMAS TO HUMAN-CHROMOSOME-7Q IN 4 FAMILIES OF MEXICAN-AMERICAN DESCENT
    Neurology
    
    M.H. Polymeropoulos et al., "LINKAGE OF THE LOCUS FOR CEREBRAL CAVERNOUS HEMANGIOMAS TO HUMAN-CHROMOSOME-7Q IN 4 FAMILIES OF MEXICAN-AMERICAN DESCENT", Neurology, 48(3), 1997, pp. 752-757
17. CAMACHO JA; GOODMAN BK; HAMOSH A; HURKO O; THOMAS GH
    MIDAS SYNDROME IN A 46,XX NEWBORN WITH AMBIGUOUS GENITALIA AND A CRYPTIC, DE-NOVO X-Y TRANSLOCATION
    American journal of human genetics
    
    J.A. Camacho et al., "MIDAS SYNDROME IN A 46,XX NEWBORN WITH AMBIGUOUS GENITALIA AND A CRYPTIC, DE-NOVO X-Y TRANSLOCATION", American journal of human genetics, 61(4), 1997, pp. 515-515
18. HURKO O
    MITOCHONDRIAL-DNA AND LEUKOENCEPHALOPATHIES
    Molecular and chemical neuropathology
    
    O. Hurko, "MITOCHONDRIAL-DNA AND LEUKOENCEPHALOPATHIES", Molecular and chemical neuropathology, 27(1), 1996, pp. 88-93
19. HURKO O; POLYMEROPOULOS MH; HSU F; RUBENSTEIN J; BASNET S; LANE K; DIETZ H; SPETZLER F; RIGAMONTI D
    LINKAGE AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CAVERNOUS HEMANGIOMAS OF THE BRAIN IN 4 MEXICAN-AMERICAN FAMILIES
    Neurology
    
    O. Hurko et al., "LINKAGE AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CAVERNOUS HEMANGIOMAS OF THE BRAIN IN 4 MEXICAN-AMERICAN FAMILIES", Neurology, 46(2), 1996, pp. 2009-2009
20. ZEE DS; VERSINO M; HURKO O
    CEREBELLAR PATIENTS HAVE OCULAR MISALIGNMENT DURING BOTH FIXATION ANDSACCADES
    Neurology
    
    D.S. Zee et al., "CEREBELLAR PATIENTS HAVE OCULAR MISALIGNMENT DURING BOTH FIXATION ANDSACCADES", Neurology, 46(2), 1996, pp. 44004-44004
21. HOFHAUS G; JOHNS DR; HURKO O; ATTARDI G; CHOMYN A
    RESPIRATION AND GROWTH DEFECTS IN TRANSMITOCHONDRIAL CELL-LINES CARRYING THE 11778-MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY
    The Journal of biological chemistry
    
    G. Hofhaus et al., "RESPIRATION AND GROWTH DEFECTS IN TRANSMITOCHONDRIAL CELL-LINES CARRYING THE 11778-MUTATION ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY", The Journal of biological chemistry, 271(22), 1996, pp. 13155-13161
22. VERSINO M; HURKO O; ZEE DS
    DISORDERS OF BINOCULAR CONTROL OF EYE-MOVEMENTS IN PATIENTS WITH CEREBELLAR DYSFUNCTION
    Brain
    
    M. Versino et al., "DISORDERS OF BINOCULAR CONTROL OF EYE-MOVEMENTS IN PATIENTS WITH CEREBELLAR DYSFUNCTION", Brain, 119, 1996, pp. 1933-1950
23. WALKUP JT; LABUDA MC; SINGER HS; BROWN J; RIDDLE MA; HURKO O
    FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTE SYNDROME - EVIDENCEFOR A MIXED-MODEL OF INHERITANCE
    American journal of human genetics
    
    J.T. Walkup et al., "FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTE SYNDROME - EVIDENCEFOR A MIXED-MODEL OF INHERITANCE", American journal of human genetics, 59(3), 1996, pp. 684-693
24. SINGER HS; LABUDA M; WALKUP J; RIDDLE M; HURKO O
    FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTES-SYNDROME - EVIDENCE FOR A MAJOR ADDITIVE LOCUS AND MULTIFACTORIAL BACKGROUND
    Annals of neurology
    
    H.S. Singer et al., "FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTES-SYNDROME - EVIDENCE FOR A MAJOR ADDITIVE LOCUS AND MULTIFACTORIAL BACKGROUND", Annals of neurology, 38(3), 1995, pp. 527-527
25. CRAWFORD TO; SLADKY JT; HURKO O; KELLEY RI
    ABNORMALITIES IN FATTY-ACID METABOLISM IN INFANTS WITH TYPE-1 SPINAL MUSCULAR-ATROPHY
    Annals of neurology
    
    T.O. Crawford et al., "ABNORMALITIES IN FATTY-ACID METABOLISM IN INFANTS WITH TYPE-1 SPINAL MUSCULAR-ATROPHY", Annals of neurology, 38(3), 1995, pp. 538-538
26. ZEIDMAN SM; MONSEIN LH; AROSARENA O; ALETICH V; BIAFORE JAM; DAWSON RC; DEBRUN GM; HURKO O
    REVERSIBILITY OF WHITE-MATTER CHANGES AND DEMENTIA AFTER TREATMENT OFDURAL FISTULAS
    American journal of neuroradiology
    
    S.M. Zeidman et al., "REVERSIBILITY OF WHITE-MATTER CHANGES AND DEMENTIA AFTER TREATMENT OFDURAL FISTULAS", American journal of neuroradiology, 16(5), 1995, pp. 1080-1083
27. BECHER MW; NOLL WW; HURKO O; PRICE DL
    NOVEL 2905-BP MITOCHONDRIAL-DNA DELETION IN KEARNS-SAYRE SYNDROME
    Journal of neuropathology and experimental neurology
    
    M.W. Becher et al., "NOVEL 2905-BP MITOCHONDRIAL-DNA DELETION IN KEARNS-SAYRE SYNDROME", Journal of neuropathology and experimental neurology, 54(3), 1995, pp. 453-453
28. WALKUP JT; LABUDA MC; HURKO O; RIDDLE MA; SINGER HS
    A FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTES-SYNDROME - EVIDENCE FOR A MIXED-MODEL OF INHERITANCE
    American journal of human genetics
    
    J.T. Walkup et al., "A FAMILY STUDY AND SEGREGATION ANALYSIS OF TOURETTES-SYNDROME - EVIDENCE FOR A MIXED-MODEL OF INHERITANCE", American journal of human genetics, 57(4), 1995, pp. 993-993
29. SPENCER F; HUGERAT Y; SIMCHEN G; HURKO O; CONNELLY C; HIETER P
    YEAST KAR1 MUTANTS PROVIDE AN EFFECTIVE METHOD FOR YAC TRANSFER TO NEW HOSTS
    Genomics
    
    F. Spencer et al., "YEAST KAR1 MUTANTS PROVIDE AN EFFECTIVE METHOD FOR YAC TRANSFER TO NEW HOSTS", Genomics, 22(1), 1994, pp. 118-126
30. HURKO O
    MITOCHONDRIAL-DNA MUTATIONS IN LEBERS OPTIC NEUROPATHY
    Annals of neurology
    
    O. Hurko, "MITOCHONDRIAL-DNA MUTATIONS IN LEBERS OPTIC NEUROPATHY", Annals of neurology, 35(5), 1994, pp. 636-636
31. BURGHES AHM; INGRAHAM SE; KOTEJARAI Z; ROSENFELD S; HERTA N; NADKARNI N; DIDONATO CJ; CARPTEN J; HURKO O; FLORENCE J; MOXLEY RT; COBBEN JM; MENDELL JR
    LINKAGE MAPPING OF THE SPINAL MUSCULAR-ATROPHY GENE
    Human genetics
    
    A.H.M. Burghes et al., "LINKAGE MAPPING OF THE SPINAL MUSCULAR-ATROPHY GENE", Human genetics, 93(3), 1994, pp. 305-312
32. UEMATSU S; WANG H; KOPITS SE; HURKO O
    TOTAL CRANIOSPINAL DECOMPRESSION IN ACHONDROPLASTIC STENOSIS
    Neurosurgery
    
    S. Uematsu et al., "TOTAL CRANIOSPINAL DECOMPRESSION IN ACHONDROPLASTIC STENOSIS", Neurosurgery, 35(2), 1994, pp. 250-257
33. DIDONATO CJ; MORGAN K; CARPTEN JD; FUERST P; INGRAHAM SE; PRESCOTT G; MCPHERSON JD; WIRTH B; ZERRES K; HURKO O; WASMUTH JJ; MENDELL JR; BURGHES AHM; SIMARD LR
    ASSOCIATION BETWEEN AG1-CA ALLELES AND SEVERITY OF AUTOSOMAL RECESSIVE PROXIMAL SPINAL MUSCULAR-ATROPHY
    American journal of human genetics
    
    C.J. Didonato et al., "ASSOCIATION BETWEEN AG1-CA ALLELES AND SEVERITY OF AUTOSOMAL RECESSIVE PROXIMAL SPINAL MUSCULAR-ATROPHY", American journal of human genetics, 55(6), 1994, pp. 1218-1229
34. LEBO RV; CHANCE PF; DYCK PJ; REDILAFLORES MT; LYNCH ED; GOLBUS MS; BIRD TD; KING MC; ANDERSON LA; HALL J; WIEGANT J; JIANG ZR; DAZIN PF; PUNNETT HH; SCHONBERG SA; MOORE K; SHULL MM; GENDLER S; HURKO O; LOVELACE RE; LATOV N; TROFATTER J; CONNEALLY PM
    CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)
    Human genetics
    
    R.V. Lebo et al., "CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)", Human genetics, 91(3), 1993, pp. 301-301
35. LEBO RV; MARTELLI L; SU Y; LI LY; LYNCH E; MANSFIELD E; PUA KH; WATSON DF; CHUEH J; HURKO O
    PRENATAL-DIAGNOSIS OF CHARCOT-MARIE-TOOTH DISEASE TYPE-1A BY MULTICOLOR IN-SITU HYBRIDIZATION
    American journal of medical genetics
    
    R.V. Lebo et al., "PRENATAL-DIAGNOSIS OF CHARCOT-MARIE-TOOTH DISEASE TYPE-1A BY MULTICOLOR IN-SITU HYBRIDIZATION", American journal of medical genetics, 47(3), 1993, pp. 441-450
36. NADKARNI N; INGRAHAM S; KOLE J; DIDONATO C; ROSENFELD S; HERTA N; HURKO O; HYSER C; FLORENCE J; FISCHBECK K; MENDELL JR; BURGHES AHM
    LINKAGE ANALYSIS OF SPINAL MUSCULAR-ATROPHY
    Neurology
    
    N. Nadkarni et al., "LINKAGE ANALYSIS OF SPINAL MUSCULAR-ATROPHY", Neurology, 43(4), 1993, pp. 210-210
37. YONEDA M; CHOMYN A; MARTINUZZI A; HURKO O; ATTARDI G
    MARKED REPLICATIVE ADVANTAGE OF MTDNA CARRYING A POINT MUTATION THAT CAUSES THE MELAS SYNDROME
    Neurology
    
    M. Yoneda et al., "MARKED REPLICATIVE ADVANTAGE OF MTDNA CARRYING A POINT MUTATION THAT CAUSES THE MELAS SYNDROME", Neurology, 43(4), 1993, pp. 402-403
38. FRANCOMANO CA; CARSON B; SEIDLER A; JAMES C; MATTHEWS C; MILLER D; ROIG C; HURKO O
    MORBIDITY AND MORTALITY IN ACHONDROPLASIA - EFFICACY OF PROSPECTIVE EVALUATION AND SURGICAL INTERVENTION
    American journal of human genetics
    
    C.A. Francomano et al., "MORBIDITY AND MORTALITY IN ACHONDROPLASIA - EFFICACY OF PROSPECTIVE EVALUATION AND SURGICAL INTERVENTION", American journal of human genetics, 53(3), 1993, pp. 112-112
39. LI LY; SU Y; SU X; MARTELLI L; HURKO O; SHAPIRO L; CHUEH J; LEBO RV
    IN-SITU HYBRIDIZATION WITH DIFFERENT COLOR CONTROL PROBE DETERMINES GENE ANEUPLOIDY RELIABLY
    American journal of human genetics
    
    L.Y. Li et al., "IN-SITU HYBRIDIZATION WITH DIFFERENT COLOR CONTROL PROBE DETERMINES GENE ANEUPLOIDY RELIABLY", American journal of human genetics, 53(3), 1993, pp. 1194-1194
40. THRELKELD A; MILLER NR; GOLNIK K; GRIFFIN J; KUNCL R; JOHNS D; HURKO O
    MYO-NEURO-GASTROINTESTINAL ENCEPHALOPATHY (MNGIE) SYNDROME - HISTOPATHOLOGICAL CHARACTERIZATION AND CLINICAL DESCRIPTION OF A MITOCHONDRIOPATHY ASSOCIATED WITH PTOSIS AND OPHTHALMOPARESIS
    Investigative ophthalmology & visual science
    
    A. Threlkeld et al., "MYO-NEURO-GASTROINTESTINAL ENCEPHALOPATHY (MNGIE) SYNDROME - HISTOPATHOLOGICAL CHARACTERIZATION AND CLINICAL DESCRIPTION OF A MITOCHONDRIOPATHY ASSOCIATED WITH PTOSIS AND OPHTHALMOPARESIS", Investigative ophthalmology & visual science, 33(4), 1992, pp. 1221-1221