1 |
Zandi PP, Zöllner S, Avramopoulos D, Willour VL, Chen Y, Qin ZS, Burmeister M, Miao K, Gopalakrishnan S, McEachin R, Potash JB, Depaulo JR Jr, McInnis MGFamily-based SNP association study on 8q24 in bipolar disorder. Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):612-8. | |
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Avramopoulos D, Lasseter VK, Fallin MD, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Pulver AE.Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B gene. Genet Med. 2007 Nov;9(11):745-51. | |
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Hamshere ML, Holmans PA, Avramopoulos D, Bassett SS, Blacker D, Bertram L, Wiener H, Rochberg N, Tanzi RE, Myers A, Wavrant-De Vrièze F, Go R, Fallin D, Lovestone S, Hardy J, Goate A, O'Donovan M, Williams J, Owen MJ.Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum Mol Genet. 2007 Nov 15;16(22):2703-12. Epub 2007 Aug 27. | |
4 |
Potash JB, Buervenich S, Cox NJ, Zandi PP, Akula N, Steele J, Rathe JA, Avramopoulos D, Detera-Wadleigh SD, Gershon ES, DePaulo JR Jr, Feinberg AP, McMahon FJ; NIMH Genetics Initiative Bipolar Disorder Consortium.Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1. Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):59-67. | |
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Stefanis NC, Henquet C, Avramopoulos D, Smyrnis N, Evdokimidis I, Myin-Germeys I, Stefanis CN, Van Os J.COMT Val158Met moderation of stress-induced psychosis. Psychol Med. 2007 Nov;37(11):1651-6. Epub 2007 Jul 20. | |
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Balciuniene J, Feng N, Iyadurai K, Hirsch B, Charnas L, Bill BR, Easterday MC, Staaf J, Oseth L, Czapansky-Beilman D, Avramopoulos D, Thomas GH, Borg A, Valle D, Schimmenti LA, Selleck SB.Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities. Am J Hum Genet. 2007 May;80(5):938-47. Epub 2007 Mar 20. | |
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Zandi PP, Avramopoulos D, Willour VL, Huo Y, Miao K, Mackinnon DF, McInnis MG, Potash JB, Depaulo JR. SNP fine mapping of chromosome 8q24 in bipolar disorder. Am J Med Genet B Neuropsychiatr Genet. 2007 Mar 13; [Epub ahead of print] PMID: 17357146 [PubMed - as supplied by publisher] | |
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Stefanis NC, Trikalinos TA, Avramopoulos D, Smyrnis N, Evdokimidis I, Ntzani EE, Ioannidis JP, Stefanis CN. Impact of Schizophrenia Candidate Genes on Schizotypy and Cognitive Endophenotypes at the Population Level. Biol Psychiatry. 2007 Mar 7; [Epub ahead of print] PMID: 17336946 [PubMed - as supplied by publisher] | |
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Avramopoulos D, Wang R, Valle D, Fallin MD, Bassett SS. A novel gene derived from a segmental duplication shows perturbed expression in Alzheimer's disease. Neurogenetics. 2007 Apr;8(2):111-20. PMID: 17199132 [PubMed - as supplied by publisher] | |
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Cheslack-Postava K, Fallin MD, Avramopoulos D, Connors SL, Zimmerman AW, Eberhart CG, Newschaffer CJ. Beta(2)-Adrenergic receptor gene variants and risk for autism in the AGRE cohort. Mol Psychiatry. 2007 Jan 2; [Epub ahead of print] PMID: 17199132 [PubMed - as supplied by publisher] | |
11 |
Smyrnis N, Evdokimidis I, Mantas A, Kattoulas E, Stefanis NC, Constantinidis TS, Avramopoulos D, Stefanis CN. Smooth pursuit eye movements in 1,087 men: effects of schizotypy, anxiety, and depression. Exp Brain Res. 2006 Nov 30; [Epub ahead of print] PMID: 17136523 [PubMed - as supplied by publisher] | |
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Smyrnis N, Avramopoulos D, Evdokimidis I, Stefanis CN, Tsekou H, Stefanis NC. Effect of Schizotypy on Cognitive Performance and Its Tuning by COMT val(158) Met Genotype Variations in a Large Population of Young Men. Biol Psychiatry. 2006 Nov 21; [Epub ahead of print] PMID: 17123481 [PubMed - as supplied by publisher] | |
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Zandi PP, Kalaydjian A, Avramopoulos D, Shao H, Fallin MD, Newschaffer CJ. Rh and ABO maternal-fetal incompatibility and risk of autism. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141(6):643-7. PMID: 16856119 [PubMed - indexed for MEDLINE] | |
14 |
Avramopoulos D, Zandi P, Gherman A, Fallin MD, Bassett SS. Testing groups of genomic locations for enrichment in disease loci using linkage scan data: a method for hypothesis testing. Hum Genomics. 2006 Jun;2(6):345-52. | |
15 |
Bassett SS, Avramopoulos D (first two authors contributed equally), Perry RT, Wiener H, Watson B Jr, Go RC, Fallin MD. Further evidence of a maternal parent-of-origin effect on chromosome 10 in late-onset Alzheimer's disease. Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 5;141(5):537-40. | |
16 |
Fallin MD, Lasseter VK, Avramopoulos D, Nicodemus KK, Wolyniec PS, McGrath JA, Steel G, Nestadt G, Liang KY, Huganir RL, Valle D, Pulver AE. Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios. Am J Hum Genet. 2005 Dec;77(6):918-36. Epub 2005 Oct 28. | |
17 |
Stefanis NC, van Os J, Avramopoulos D, Smyrnis N, Evdokimidis I, Stefanis CN. Effect of COMT Val158Met polymorphism on the Continuous Performance Test, Identical Pairs Version: tuning rather than improving performance. Am J Psychiatry. 2005 Sep;162(9):1752-4. | |
18 |
Bassett SS, Kusevic I, Cristinzio C, Yassa MA, Avramopoulos D, Yousem DM, Fallin MD. Brain activation in offspring of AD cases corresponds to 10q linkage. Ann Neurol. 2005 Jul;58(1):142-6. | |
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Stefanis NC, Van Os J, Avramopoulos D, Smyrnis N, Evdokimidis I, Hantoumi I, Stefanis CN. Variation in catechol-o-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men. Biol Psychiatry. 2004 Oct 1;56(7):510-5. | |
20 |
Avramopoulos D, Fallin MD, Bassett SS (2005). Linkage to chromosome 14q in Alzheimer’s Disease (AD) patients without psychotic symptoms. Am J Med Genet Neuropsy Genet 2005 Jan 5;132(1):9-13. | |
21 |
Stefanis NC, Van Os J, Avramopoulos D, Smyrnis N, Evdokimidis I, Hantoumi I, Stefanis CN (2004). Variation in catechol-o-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men. Biol Psychiatry 56(7):510-5. | |
22 |
Stefanis NC, Smyrnis N, Avramopoulos D, Evdokimidis I, Ntzoufras I, Stefanis CN (2004). Factorial composition of self-rated schizotypal traits among young males undergoing military training. Schizophr Bull. 30(2):335-50. Review. | |
23 |
Stefanis NC, Delespaul P, Smyrnis N, Lembesi A, Avramopoulos D, Evdokimidis IK, Stefanis CN, van Os J. (2004) Is the excess risk of psychosis-like experiences in urban areas attributable to altered cognitive development? Soc Psychiatry Psychiatr Epidemiol. May;39(5):364-8. | |
24 |
Avramopoulos D, Willour VL, Zandi PP, Huo Y, MacKinnon DF, Potash JB, DePaulo JR Jr, McInnis MG (2004). Linkage of bipolar affective disorder on chromosome 8q24: follow-up and parametric analysis. Mol Psychiatry 9(2):191-6 | |
25 |
Smyrnis N, Kattoulas E, Evdokimidis I, Stefanis NC, Avramopoulos D, Pantes G, Theleritis C, Stefanis CN (2003). Active eye fixation performance in 940 young men: effects of IQ, schizotypy, anxiety and depression. Exp Brain Res. 2004 May;156(1):1-10. Epub 2003 Dec 19. | |
26 |
McInnis MG, Dick DM, Willour VL, Avramopoulos D, MacKinnon DF, Simpson SG, Potash JB, Edenberg HJ, Bowman ES, McMahon FJ, Smiley C, Chellis JL, Huo Y, Diggs T, Meyer ET, Miller M, Matteini AT, Rau NL, DePaulo JR, Gershon ES, Badner JA, Rice JP, Goate AM, Detera-Wadleigh SD, Nurnberger JI, Reich T, Zandi PP, Foroud TM (2003). Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees. Biol Psychiatry 54(11):1265-73. | |
27 |
Papadimitriou GN, Dikeos DG, Souery D, Del-Favero J, Massat I, Avramopoulos D, Blairy S, Cichon S, Ivezic S, Kaneva R, Karadima G, Lilli R, Milanova V, Nothen M, Oruc L, Rietschel M, Serretti A, Van Broeckhoven C, Stefanis CN, Mendlewicz J. (2003) Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case-control study. Psychiatr Genet. 13(4):211-20. | |
28 |
Smyrnis N, Evdokimidis I, Stefanis NC, Avramopoulos D, Constantinidis TS, Stavropoulos A, Stefanis CN (2003). Antisaccade performance of 1,273 men: effects of schizotypy, anxiety, and depression. J Abnorm Psychol. 112(3):403-14. | |
29 |
Constantinidis TS, Smyrnis N, Evdokimidis I, Stefanis NC, Avramopoulos D, Giouzelis I, Stefanis CN (2003). Effects of direction on saccadic performance in relation to lateral preferences. Exp Brain Res. 150(4):443-8. | |
30 |
Potash JB, Zandi PP, Willour VL, Lan TH, Huo Y, Avramopoulos D, Shugart YY, MacKinnon DF, Simpson SG, McMahon FJ, DePaulo JR Jr, McInnis MG. (2003) Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. Am J sychiatry.160(4):680-6. | |
31 |
Blacker D, Bertram L, Saunders AJ, Moscarillo TJ, Albert MS, Wiener H, Perry RT, Collins JS, Harrell LE, Go RC, Mahoney A, Beaty T, Fallin MD, Avramopoulos D, Chase GA, Folstein MF, McInnis MG, Bassett SS, Doheny KJ, Pugh EW, Tanzi RE (2003). Results of a high-resolution genome screen of 437 Alzheimer's Disease families. Hum Mol Genet. 12(1):23-32. | |
32 |
Smyrnis N, Evdokimidis I, Stefanis NC, Constantinidis TS, Avramopoulos D, Theleritis C, Paximadis C, Efstratiadis C, Kastrinakis G, Stefanis CN (2002). The antisaccade task in a sample of 2,006 young males II. Effects of task parameters. Exp Brain Res. 147(1):53-63. | |
33 |
Evdokimidis I, Smyrnis N, Constantinidis TS, Stefanis NC, Avramopoulos D, Paximadis C, Theleritis C, Efstratiadis C, Kastrinakis G, Stefanis CN (2002). The antisaccade task in a sample of 2,006 young men I. Normal population characteristics. Exp Brain Res. 147(1):45-52. | |
34 |
Bassett SS,1 Avramopoulos D, Fallin MD (2002). Evidence for parent of origin effect in late- onset Alzheimer’s disease . Am J Med Genet. 8;114(6):679-86. | |
35 |
Avramopoulos D, Stefanis NC, Hantoumi I, Smyrnis N, Evdokimidis I and Stefanis CN (2002). Higher scores of self reported schizotypy in healthy young males carrying the COMT high activity allele. Mol Psychiatry 7(7):706-11. | |
36 |
Stefanis NC, Hanssen M , Smyrnis N, Avramopoulos D, Evdokimidis I, Stefanis CN, Verdoux H, van Os J. (2002). Evidence that three dimensions of psychosis have a distribution in the general population. Psychol Med 32(2):347-58. | |
37 |
Papadimitriou G, Dikeos DG, Karadima G, Avramopoulos D, Daskalopoulou EG, Stefanis C (2001). GABA-A Receptor Beta3 and Alpha5 Subunit Gene Cluster on Chromosome 15q11-q13 and Bipolar Disorder: A Genetic Association Study. Am J Med Genet 105(4):317-20. | |
38 |
Papadimitriou G, Dikeos DG, Daskalopoulou EG, Karadima G, Avramopoulos D, Kontis C, Stefanis C (2001). Association between the GABAA Receptor 5 Subunit gene locus (GABRA5) and Schizophrenia of a later age of onset. Neuropsychobiology 43(3):141-4. | |
39 |
Petersen MB, Karadima G, Samaritaki M, Avramopoulos D, Vassilopoulos D, Mikkelsen M (2000). Association between Presenilin-1 polymorphism and maternal meiosis II errors in Down's syndrome Am J Med Genet 93:366-372. | |
40 |
Barbi G, Kennerknecht I, Wohr G, Avramopoulos D, Karadima G, Petersen MB (2000). Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype. Am J Med Genet. 91(2):116-22. | |
41 |
Dikeos DG, Papadimitriou GN, Avramopoulos D, Karadima G, Daskalopoulou EG, Souery D, Mendlewicz J, Vassilopoulos D, Stefanis CN (1999). Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder. Psychiatr Genet 9(4):189-95. | |
42 |
Karadimas C, Panas M, Chronopoulou P, Avramopoulos D, Vassilopoulos D (1999). Three novel mutations in the gap junction beta 1 (GJB1) gene coding region identified in Charcot-Marie-Tooth patients of Greek origin: T55I, R164Q, V120E. Mutation in brief no 236. Online. Hum Mutat. 13(4):339. | |
43 |
Panas M, Avramopoulos D, Karadima G, Petersen MB, Vassilopoulos D (1999). Apolipoprotein E and Presenilin-1 genotypes in Huntington’s disease J Neurol. 246(7):574-7. | |
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Savage R, Petersen MB, Pettay D, Taft L, Allran K, Freeman SB, Karadima G, Avramopoulos D, Torts C, Mikkelsen M, Hassold TJ, Sherman SI (1998). Elucidating the mechanisms of paternal nondisjunction of chromosome 21 in humans. Hum Mol Genet. Aug;7(8):1221-7. | |
45 |
Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Anneren G, Blennow E, Clausen N, Galla -Voumvouraki A,Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Lacombe D, Miller K, Moncla A, Pajares IL, Patsalis PH.C, Prieur M, Vekemans M, Beust G, Brondum-Nielsen K, Petersen MB (1998). Origin of nondijunction in trisomy 8 and trisomy 8 mosaicism. Eur J Hum Genet. 6(5):432-8. | |
46 |
Panas M, Karadimas C, Avramopoulos D, Vassilopoulos D (1998). Central Nervous System involvement in four Charcot-Marie-Tooth patients with connexin 32 extracellular mutations. J Neurol Neurosurg Psychiatry.65(6):947-8. | |
47 |
Papadimitriou GN, Dikeos DG, Karadima G, Avramopoulos D, Daskalopoulou EG, Vassilopoulos D, Stefanis CN (1998). Association between the GABA(A) receptor alpha5 subunit gene locus (GABRA5) and bipolar affective disorder. Am J Med Genet, 81:73-80. | |
48 |
Sarri C, Gyftodimou J, Avramopoulos D, Grigoriadou M, Pedersen W, Pandelia E, Pangalos C, Abazis D, Kitsos G, Vassilopoulos D, Brondum-Nielsen K, Petersen MB (1997). Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter. Am J Med Genet, 70(1):87-94. | |
49 |
Avramopoulos D, Kennerknecht I, Barbi G, Eckert D, Delabar JM, Maunoury C, Hallberg A, Petersen MB (1997). A case of apparent trisomy 21 without the Down syndrome phenotype. J Med Genet, 34(7):597-600. | |
50 |
Lamb NE, Feingold E, Savage-Austin A, Karadima G, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL (1997). Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosomne 21. Hum Mol Genet, 6(9):1391-1399. | |
51 |
Bartsch O, Hinkel GK, Petersen MB, Konig U, Bugge M, Mikkelsen M, Avramopoulos D, Morris M, Antonarakis SE (1997). A large family with subtelomeric translocation t(18;21)(q23;q22.13) and molecular breakpoint in the Down syndrome critical region. Hum Genet, 100(5-6):669-675. | |
52 |
Sklavounou E, Economou-Petersen E, Karadima G, Panas M, Avramopoulos D, Varsou A, Vassilopoulos D, Petersen MB (1997). Apolipoprotein E polymorphism in the Greek population. Clin Genet, 52(4):216-218. | |
53 |
Lamb NE, Freeman SB, Savage-Austin A, Pettay D, Taft L, Hersey J, Gu Y, Shen J, Saker D, May KM, Avramopoulos D, Petersen MB, Hallberg A, Mikkelsen M, Hassold TJ, Sherman SL (1996). Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat Genet, 14:400-405. | |
54 |
Bugge M, Blennow E, Friedrich U, Petersen MB, Pedeutour F, Tsezou A, Orum A, Hermann S, Lyngbye T, Sarri C, Avramopoulos D, Kitsiou S, Lambert JC, Guzda M, Tommerup N, Brondum-Nielsen K (1996). Tetrasomy 18p de novo: parental origin and different mechanisms of formation. Eur J Hum Genet, 4:160-167. | |
55 |
Avramopoulos D, Mikkelsen M, Vassilopoulos D, Grigoriadou M, Petersen MB (1996). Apolipoprotein E allele distribution in parents of Down's syndrome children. Lancet, 347:862-865. | |
56 |
Avramopoulos D, Kitsos G, Economou-Petersen E, Grigoriadou M, Vassilopoulos D, Papageorgiou C, Psilas K, Petersen MB (1996). Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31. J Med Genet, 33:1043-1044. | |
57 |
Talbot CC Jr, Avramopoulos D, Gerken S, Chakravarti A, Armour JA, Matsunami N, White R and Antonarakis SE (1995). The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells. Hum Mol Genet, 4:1193-1199. | |
58 |
Chen H, Lowther W, Avramopoulos D, Antonarakis SE. (1994). Homologous Loci DXYS156X and DXYS156Y, Contain a Polymorphic Pentanucleotide Repeat (TAAAA)n and Map to Human X and Y Chromosomes. Hum Mutat, 4:208-211. | |
59 |
Pangalos C, Avramopoulos D (First two authors contributed equally to the study: Am J Hum Genet 55:217 errata), Blouin JL, Raoul O, deBlois MC, Prieur M, Schinzel, AA, Gika M, Abazis D, Antonarakis SE (1994). Understanding the Mechanism(s) of Mosaic for Trisomy 21 Using DNA Polymorphism Analysis. Am J Hum Genet, 54:473-481. | |
60 |
Blouin JL, Avramopoulos D, Pangalos C, Antonarakis SE (1994). Normal Phenotype with Paternal Uniparental Isodisomy for Chromosome 21. Am J Hum Genet, 53:1074-1078. | |
61 |
Chen H, Kalaitsidaki M, Warren AC, Avramopoulos D, Antonarakis SE (1993). A Novel Zinc Finger cDNA with a Polymorphic Pentanucleotide Repeat (ATTTT)n Maps on Human Chromosome 19p. Genomics, 15:621 - 625. | |
62 |
Petersen MB, Antonarakis SE, Hassold TJ, Freeman SB, Sherman SL, Avramopoulos D and Mikkelsen M (1993). Paternal nondisjunction in trisomy 21; No maternal age effect and excess of male patients. Hum Mol Genet, 2(10):1691-1695. | |
63 |
McInnis MG, Chakravarti A, Blaschak J, Petersen MB, Sharma V, Avramopoulos D, Blouin JL, Konig U, Brahe C, Cox T, Warren AC, Talbot CC, Van Broeckhoven C, Litt M, Antonarakis SE (1993). A Linkage Map of Human Chromosome 21 : 43 PCR Μarkers at Average Intervals of 2.5 cM. Genomics 16:562-571. | |
64 |
Talbot CC Jr, Warren AC, Avramopoulos D, Antonarakis SE (1993). Polymorphic Dinucleotide Repeats at the D3S1417, D3S1418 and D12S271 Loci. Hum Mol Genet, 2:1325 | |
65 |
Antonarakis SE, Avramopoulos D, Blouin JL, Talbot CC and Schinzel AA (1993). Mitotic Errors in Somatic Cells Cause Trisomy 21 in about 4.5% of Cases and are Not Associated with Advanced Maternal Age. Nat Genet 3:146-150. | |
66 |
Avramopoulos D, Chakravarti A, and Antonarakis SE (1993). DNA Polymorphisms in the 3'Untranslated Region of Genes on Human Chromosome 21. Genomics, 15:98-102. | |
67 |
Avramopoulos D, Cox T, Kraus JP, Chakravarti A, Antonarakis SE (1993). Linkage Mapping of the Cystathionine Beta Synthase Gene on Human Chromosome 21 Using a Polymorphism in the 3'Untranslated Region. Hum Genet 90(5):566-568. | |
68 |
Antonarakis SE, Blouin JL, Maher J, Avramopoulos D, Thomas G, Talbot CC (1992). Maternal Uniparental Disomy for Human Chromosome 14 Due to Loss of a Chromosome 14 from Somatic Cells with Trisomy 14. Am J Hum Genet, 52:1145-1152. | |
69 |
NIH/CEPH Collaborative Mapping Group (chromosome 21 : Antonarakis SE, Chakravarti A, McInnis MG, Sharma V, Avramopoulos D, Blaschak J, Litt M, Blouin JL) (1992). A Comprehensive Linkage Map of the Human Genome. Science, 285:67-86. | |
70 |
Avramopoulos D, Cox T, Chakravarti A, Antonarakis SE (1992). Linkage Mapping of the AML1 gene on Human Chromosome 21 Using a Polymorphism in the 3'Untranslated Region. Genomics, 14:506-507. | |
71 |
Avramopoulos D, Cox T, Forrest GL, Chakravarti A, Antonarakis SE (1992). Linkage Mapping of the Carbonyl Reductase Gene on Human Chromosome 21 Using a DNA Polymorphism in the 3'Untranslated Region. Genomics 13:447-448. |
