| Year |
Citation |
Score |
| 2020 |
Zhang S, Zhang X, Purmann C, Ma S, Shrestha A, Davis KN, Ho M, Huang Y, Pattni R, Wong WH, Bernstein JA, Hallmayer J, Urban AE. Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons. Biological Psychiatry. PMID 32919612 DOI: 10.1016/J.Biopsych.2020.06.021 |
0.345 |
|
| 2020 |
Zhang X, Hong D, Ma S, Ward T, Ho M, Pattni R, Duren Z, Stankov A, Bade Shrestha S, Hallmayer J, Wong WH, Reiss AL, Urban AE. Integrated functional genomic analyses of Klinefelter and Turner syndromes reveal global network effects of altered X chromosome dosage. Proceedings of the National Academy of Sciences of the United States of America. PMID 32071206 DOI: 10.1073/Pnas.1910003117 |
0.3 |
|
| 2019 |
Hallmayer J, Bernstein J, O'Hara R, Pasca S. Ipscs - A Platform To Study Autism Spectrum Disorder European Neuropsychopharmacology. 29: S764-S765. DOI: 10.1016/J.Euroneuro.2017.06.121 |
0.374 |
|
| 2017 |
Chang K, Garrett A, Kelley R, Howe M, Sanders EM, Acquaye T, Bararpour L, Li S, Singh M, Jo B, Hallmayer J, Reiss A. Anomalous prefrontal-limbic activation and connectivity in youth at high-risk for bipolar disorder. Journal of Affective Disorders. 222: 7-13. PMID 28667891 DOI: 10.1016/J.Jad.2017.05.051 |
0.302 |
|
| 2017 |
C Yuen RK, Merico D, Bookman M, L Howe J, Thiruvahindrapuram B, Patel RV, Whitney J, Deflaux N, Bingham J, Wang Z, Pellecchia G, Buchanan JA, Walker S, Marshall CR, Uddin M, ... ... Hallmayer J, et al. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nature Neuroscience. PMID 28263302 DOI: 10.1038/Nn.4524 |
0.385 |
|
| 2015 |
Li J, Ma Z, Shi M, Malty RH, Aoki H, Minic Z, Phanse S, Jin K, Wall DP, Zhang Z, Urban AE, Hallmayer J, Babu M, Snyder M. Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders. Cell Systems. 1: 361-374. PMID 26949739 DOI: 10.1016/J.Cels.2015.11.002 |
0.304 |
|
| 2015 |
Park MH, Sanders E, Howe M, Singh M, Hallmayer J, Kim E, Chang K. Association of Anxiety Symptoms in Offspring of Bipolar Parents with Serotonin Transporter-Linked Polymorphic Region (5-HTTLPR) Genotype. Journal of Child and Adolescent Psychopharmacology. 25: 458-66. PMID 26218602 DOI: 10.1089/Cap.2014.0115 |
0.315 |
|
| 2015 |
Park MH, Chang KD, Hallmayer J, Howe ME, Kim E, Hong SC, Singh MK. Preliminary study of anxiety symptoms, family dysfunction, and the brain-derived neurotrophic factor (BDNF) Val66Met genotype in offspring of parents with bipolar disorder. Journal of Psychiatric Research. 61: 81-8. PMID 25498133 DOI: 10.1016/J.Jpsychires.2014.11.013 |
0.351 |
|
| 2014 |
Li J, Shi M, Ma Z, Zhao S, Euskirchen G, Ziskin J, Urban A, Hallmayer J, Snyder M. Integrated systems analysis reveals a molecular network underlying autism spectrum disorders. Molecular Systems Biology. 10: 774. PMID 25549968 DOI: 10.15252/Msb.20145487 |
0.313 |
|
| 2014 |
Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, et al. The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. Molecular Autism. 5: 34. PMID 25392729 DOI: 10.1186/2040-2392-5-34 |
0.311 |
|
| 2014 |
O'Hara R, Hallmayer J. Coming of age of genetic investigations in late-life mental health. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. 22: 953-6. PMID 25217024 DOI: 10.1016/J.Jagp.2014.07.004 |
0.333 |
|
| 2014 |
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... Hallmayer J, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.372 |
|
| 2014 |
Froehlich-Santino W, Londono Tobon A, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, ... ... Hallmayer J, et al. Prenatal and perinatal risk factors in a twin study of autism spectrum disorders. Journal of Psychiatric Research. 54: 100-8. PMID 24726638 DOI: 10.1016/J.Jpsychires.2014.03.019 |
0.306 |
|
| 2013 |
Han F, Faraco J, Dong XS, Ollila HM, Lin L, Li J, An P, Wang S, Jiang KW, Gao ZC, Zhao L, Yan H, Liu YN, Li QH, Zhang XZ, ... ... Hallmayer J, et al. Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. Plos Genetics. 9: e1003880. PMID 24204295 DOI: 10.1371/Journal.Pgen.1003880 |
0.319 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Hallmayer J, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.346 |
|
| 2013 |
Faraco J, Lin L, Kornum BR, Kenny EE, Trynka G, Einen M, Rico TJ, Lichtner P, Dauvilliers Y, Arnulf I, Lecendreux M, Javidi S, Geisler P, Mayer G, Pizza F, ... ... Hallmayer J, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Plos Genetics. 9: e1003270. PMID 23459209 DOI: 10.1371/Journal.Pgen.1003270 |
0.319 |
|
| 2013 |
Froehlich W, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, ... Hallmayer J, et al. Head circumferences in twins with and without Autism Spectrum Disorders. Journal of Autism and Developmental Disorders. 43: 2026-37. PMID 23321801 DOI: 10.1007/S10803-012-1751-1 |
0.314 |
|
| 2013 |
Miller S, Hallmayer J, Wang PW, Hill SJ, Johnson SL, Ketter TA. Brain-derived neurotrophic factor val66met genotype and early life stress effects upon bipolar course. Journal of Psychiatric Research. 47: 252-8. PMID 23182421 DOI: 10.1016/J.Jpsychires.2012.10.015 |
0.325 |
|
| 2013 |
Zhang B, Choi Y, Ng D, Weng Z, Lo C, Ghebremariam Y, Özkan E, Liao C, Inoue S, Hallmayer J, Garcia C, Cooke J, Tang H, Sidow A, Zehnder JL. Identification Of The Disease-Causing Mutation In Autosomal Dominant Familial Immune Thrombocytopenia By Genome-Wide Linkage Analysis and Whole Genome Sequencing Blood. 122: 565-565. DOI: 10.1182/Blood.V122.21.565.565 |
0.368 |
|
| 2012 |
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Hallmayer J, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301 |
0.365 |
|
| 2012 |
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... ... Hallmayer J, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/S00439-011-1094-6 |
0.394 |
|
| 2011 |
Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, et al. Genetic heritability and shared environmental factors among twin pairs with autism. Archives of General Psychiatry. 68: 1095-102. PMID 21727249 DOI: 10.1001/Archgenpsychiatry.2011.76 |
0.322 |
|
| 2011 |
Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P. Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Journal of Neurodevelopmental Disorders. 3: 113-23. PMID 21484201 DOI: 10.1007/S11689-011-9072-9 |
0.402 |
|
| 2011 |
Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, ... ... Hallmayer J, et al. Common variants in P2RY11 are associated with narcolepsy. Nature Genetics. 43: 66-71. PMID 21170044 DOI: 10.1038/Ng.734 |
0.305 |
|
| 2011 |
Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, et al. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of Medical Genetics. 48: 48-54. PMID 20972252 DOI: 10.1136/Jmg.2010.079426 |
0.393 |
|
| 2010 |
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Hallmayer J, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307 |
0.367 |
|
| 2010 |
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Hallmayer J, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.374 |
|
| 2010 |
Chandler D, Dragović M, Cooper M, Badcock JC, Mullin BH, Faulkner D, Wilson SG, Hallmayer J, Howell S, Rock D, Palmer LJ, Kalaydjieva L, Jablensky A. Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 428-37. PMID 19569075 DOI: 10.1002/Ajmg.B.30996 |
0.341 |
|
| 2009 |
Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Hong SS, Honda Y, Honda M, Högl B, et al. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nature Genetics. 41: 708-11. PMID 19412176 DOI: 10.1038/Ng.372 |
0.337 |
|
| 2009 |
Chen MC, Joormann J, Hallmayer J, Gotlib IH. Serotonin transporter polymorphism predicts waking cortisol in young girls. Psychoneuroendocrinology. 34: 681-6. PMID 19128885 DOI: 10.1016/J.Psyneuen.2008.11.006 |
0.318 |
|
| 2009 |
Kaneva R, Milanova V, Angelicheva D, MacGregor S, Kostov C, Vladimirova R, Aleksiev S, Angelova M, Stoyanova V, Loh A, Hallmayer J, Kalaydjieva L, Jablensky A. Bipolar disorder in the Bulgarian Gypsies: genetic heterogeneity in a young founder population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 191-201. PMID 18444255 DOI: 10.1002/Ajmg.B.30775 |
0.39 |
|
| 2008 |
Gotlib IH, Joormann J, Minor KL, Hallmayer J. HPA axis reactivity: a mechanism underlying the associations among 5-HTTLPR, stress, and depression. Biological Psychiatry. 63: 847-51. PMID 18005940 DOI: 10.1016/J.Biopsych.2007.10.008 |
0.308 |
|
| 2007 |
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Hallmayer J, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.405 |
|
| 2006 |
Wong D, Maybery M, Bishop DV, Maley A, Hallmayer J. Profiles of executive function in parents and siblings of individuals with autism spectrum disorders. Genes, Brain, and Behavior. 5: 561-76. PMID 17081261 DOI: 10.1111/J.1601-183X.2005.00199.X |
0.304 |
|
| 2006 |
Baumer FM, Howe M, Gallelli K, Simeonova DI, Hallmayer J, Chang KD. A pilot study of antidepressant-induced mania in pediatric bipolar disorder: Characteristics, risk factors, and the serotonin transporter gene. Biological Psychiatry. 60: 1005-12. PMID 16945343 DOI: 10.1016/J.Biopsych.2006.06.010 |
0.324 |
|
| 2006 |
Larkin EK, Patel SR, Redline S, Mignot E, Elston RC, Hallmayer J. Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak. Genetic Epidemiology. 30: 101-10. PMID 16374834 DOI: 10.1002/Gepi.20127 |
0.329 |
|
| 2004 |
Nair-Miranda K, Murch A, Petterson B, Hill W, Nikolova-Hill A, Bradley L, Jackson S, Hallmayer J. An investigation into sub-telomeric deletions of chromosome 22 and pervasive developmental disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 99-104. PMID 14755453 DOI: 10.1002/Ajmg.B.20101 |
0.3 |
|
| 2004 |
Sporn A, Addington A, Reiss AL, Dean M, Gogtay N, Potocnik U, Greenstein D, Hallmayer J, Gochman P, Lenane M, Baker N, Tossell J, Rapoport JL. 22q11 deletion syndrome in childhood onset schizophrenia: an update Molecular Psychiatry. 9: 225-226. PMID 14699434 DOI: 10.1038/Sj.Mp.4001477 |
0.304 |
|
| 2003 |
Schwab SG, Mondabon S, Knapp M, Albus M, Hallmayer J, Borrmann-Hassenbach M, Trixler M, Gross M, Schulze TG, Rietschel M, Lerer B, Maier W, Wildenauer DB. Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia. Schizophrenia Research. 65: 19-25. PMID 14623370 DOI: 10.1016/S0920-9964(02)00534-0 |
0.382 |
|
| 2003 |
Schwab SG, Knapp M, Mondabon S, Hallmayer J, Borrmann-Hassenbach M, Albus M, Lerer B, Rietschel M, Trixler M, Maier W, Wildenauer DB. Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. American Journal of Human Genetics. 72: 185-90. PMID 12474144 DOI: 10.1086/345463 |
0.409 |
|
| 2002 |
Hallmayer J, Glasson EJ, Bower C, Petterson B, Croen L, Grether J, Risch N. On the twin risk in autism. American Journal of Human Genetics. 71: 941-6. PMID 12297988 DOI: 10.1086/342990 |
0.33 |
|
| 2002 |
Laws SM, Clarnette RM, Taddei K, Martins G, Paton A, Hallmayer J, Almeida OP, Groth DM, Gandy SE, Förstl H, Martins RN. APOE-epsilon4 and APOE -491A polymorphisms in individuals with subjective memory loss. Molecular Psychiatry. 7: 768-75. PMID 12192621 DOI: 10.1038/Sj.Mp.4001083 |
0.309 |
|
| 2002 |
Schwab SG, Hallmayer J, Freimann J, Lerer B, Albus M, Borrmann-Hassenbach M, Segman RH, Trixler M, Rietschel M, Maier W, Wildenauer DB. Investigation of linkage and association/linkage disequilibrium of HLA A-, DQA1-, DQB1-, and DRB1-alleles in 69 sib-pair- and 89 trio-families with schizophrenia. American Journal of Medical Genetics. 114: 315-20. PMID 11920855 DOI: 10.1002/Ajmg.10307 |
0.389 |
|
| 2002 |
Merlini L, Gooding R, Lochmuller H, Muller-Felber W, Walter MC, Angelicheva D, Talim B, Hallmayer J, Kalaydjieva L. Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes. Neurology. 58: 231-236. PMID 11805249 DOI: 10.1212/Wnl.58.2.231 |
0.372 |
|
| 2001 |
Sklar P, Schwab SG, Williams NM, Daly M, Schaffner S, Maier W, Albus M, Trixler M, Eichhammer P, Lerer B, Hallmayer J, Norton N, Williams H, Zammit S, Cardno AG, et al. Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls. Nature Genetics. 28: 126-8. PMID 11381257 DOI: 10.1038/88836 |
0.364 |
|
| 2000 |
Hallmayer J. The epidemiology of the genetic liability for schizophrenia. Australian and New Zealand Journal of Psychiatry. 34. PMID 11129315 DOI: 10.1080/000486700222 |
0.353 |
|
| 2000 |
Schwab SG, Hallmayer J, Albus M, Lerer B, Eckstein GN, Borrmann M, Segman RH, Hanses CA, Freymann J, Yakir A, Trixler M, Falkai P, Rietschel M, Maier W, Wildenauer DB. A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: Support for loci on chromosome 10p and 6 Molecular Psychiatry. 5: 638-649. PMID 11126394 DOI: 10.1038/Sj.Mp.4000791 |
0.365 |
|
| 2000 |
Wilson SG, Spector T, Taylor AL, Retallack RW, Henderson K, Hallmayer J, Prince RL. Linkage analysis of four candidate genes using osteoporosis affected sib pairs Bone. 27: 26. DOI: 10.1016/S8756-3282(00)80087-3 |
0.304 |
|
| 1999 |
Schwab SG, Wildenauer DB, Hallmayer J. No evidence for segregation distortion in females in a sample of 72 families with schizophrenia with potential linkage to chromosome 10p14-p11. American Journal of Medical Genetics. 88: 750-751. PMID 10581501 DOI: 10.1002/(Sici)1096-8628(19991215)88:6<750::Aid-Ajmg30>3.0.Co;2-U |
0.336 |
|
| 1999 |
Kalaydjieva L, Perez-Lezaun A, Angelicheva D, Onengut S, Dye D, Bosshard NU, Jordanova A, Savov A, Yanakiev P, Kremensky I, Radeva B, Hallmayer J, Markov A, Nedkova V, Tournev I, et al. A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies). American Journal of Human Genetics. 65: 1299-307. PMID 10521295 DOI: 10.1086/302611 |
0.324 |
|
| 1999 |
Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, et al. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. American Journal of Medical Genetics. 88: 551-6. PMID 10490715 DOI: 10.1002/(SICI)1096-8628(19991015)88:5<551::AID-AJMG21>3.0.CO;2-# |
0.365 |
|
| 1999 |
Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C, McMahon WM, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Peachy T, Yang J, et al. Exclusion of linkage to the HLA region in ninety multiplex sibships with autism. Journal of Autism and Developmental Disorders. 29: 195-201. PMID 10425582 DOI: 10.1023/A:1023075904742 |
0.385 |
|
| 1999 |
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, et al. A genomic screen of autism: evidence for a multilocus etiology. American Journal of Human Genetics. 65: 493-507. PMID 10417292 DOI: 10.1086/302497 |
0.35 |
|
| 1999 |
Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 174-9. PMID 10406984 DOI: 10.1136/Jnnp.67.2.174 |
0.319 |
|
| 1999 |
Schwab SG, Wildenauer DB, Collier DA, Ekelund A, Gejman P, Hallmayer J, Kelsoe JR, Gontard Av, Wildenauer DB. Chromosome 22 workshop report. American Journal of Medical Genetics. 88: 276-278. PMID 10374745 DOI: 10.1002/(Sici)1096-8628(19990618)88:3<276::Aid-Ajmg13>3.0.Co;2-N |
0.352 |
|
| 1999 |
Felice KJ, Meredith C, Binz N, Butler A, Jacob R, Akkari P, Hallmayer J, Laing N. Autosomal dominant distal myopathy not linked to the known distal myopathy loci. Neuromuscular Disorders : Nmd. 9: 59-65. PMID 10220859 DOI: 10.1016/S0960-8966(98)00099-6 |
0.345 |
|
| 1998 |
Kaneva R, Milanova V, Onchev G, Stoyanova V, Chakarova CH, Nikolova A, Hallmayer J, Belemezova M, Milenska T, Kirov G, Kremensky I, Kalaydjieva L, Jablensky A. A linkage study of affective disorders in two Bulgarian Gypsy families: Results for candidate regions on chromosomes 18 and 21 Psychiatric Genetics. 8: 245-249. PMID 9861644 DOI: 10.1097/00041444-199808040-00008 |
0.357 |
|
| 1998 |
Taddei K, Yang D, Fisher C, Clarnette R, Hallmayer J, Barnetson R, Maller R, Brooks WS, Whyte S, Nicholson GA, Masters CL, Broe GA, Gandy SE, Martins RN. No association of presenilin-1 intronic polymorphism and Alzheimer's disease in Australia. Neuroscience Letters. 246: 178-80. PMID 9792621 DOI: 10.1016/S0304-3940(98)00248-1 |
0.307 |
|
| 1998 |
Schwab SG, Hallmayer J, Lerer B, Albus M, Borrmann M, Hönig S, Strauß M, Segman R, Lichtermann D, Knapp M, Trixler M, Maier W, Wildenauer DB. Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis. American Journal of Human Genetics. 63: 1139-1152. PMID 9758604 DOI: 10.1086/302046 |
0.369 |
|
| 1998 |
Vallada H, Curtis D, Sham P, Kunugi H, Zhao J, Murray R, McGuffin P, Nanko S, Owen M, Gill M, Collier D, Antonarakis S, Housman D, Kazazian H, Nestadt G, ... ... Hallmayer J, et al. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12 Schizophrenia Research. 32: 115-121. PMID 9713907 DOI: 10.1016/S0920-9964(98)00048-6 |
0.385 |
|
| 1998 |
Leder RO, Mansbridge JN, Hallmayer J, Hodge SE. Familial psoriasis and HLA-B: unambiguous support for linkage in 97 published families. Human Heredity. 48: 198-211. PMID 9694251 DOI: 10.1159/000022802 |
0.317 |
|
| 1998 |
Schwab SG, Hallmayer J, Albus M, Lerer B, Hanses C, Kanyas K, Segman R, Borrman M, Dreikorn B, Lichtermann D, Rietschel M, Trixler M, Maier W, Wildenauer DB. Further evidence for a susceptibility locus on chromosome 10p14-p11 in 72 families with schizophrenia by nonparametric linkage analysis. American Journal of Medical Genetics. 81: 302-307. PMID 9674975 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<302::Aid-Ajmg5>3.0.Co;2-V |
0.396 |
|
| 1998 |
Schwa SG, Knapp M, Freymann J, Albus M, Lerer B, Hallmayer J, Maier W, Wildenauer DB. The HLA DRBI gene locus in schizophrenia: An association study in 55 families with linkage to chromosome 6P Schizophrenia Research. 29: 133. DOI: 10.1016/S0920-9964(97)88637-9 |
0.38 |
|
| 1997 |
Schwab SG, Eckstein GN, Hallmayer J, Lerer B, Albus M, Borrmann M, Lichtermann D, Ertl MA, Maier W, Wildenauer DB. Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis Molecular Psychiatry. 2: 156-160. PMID 9106241 DOI: 10.1038/Sj.Mp.4000263 |
0.354 |
|
| 1996 |
Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B, Maier W, Blackwood D, Muir W, Clair DS, Morris S, Moises HW, Yang L, Kristbjarnarson H, Helgason T, Wiese C, et al. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study American Journal of Medical Genetics. 67: 580-594. PMID 8950417 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<580::Aid-Ajmg11>3.0.Co;2-P |
0.346 |
|
| 1996 |
Hallmayer J, Hebert JM, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Lin AA, Cavalli-Sforza LL, Risch N, Ciaranello RD. Autism and the X chromosome. Multipoint sib-pair analysis. Archives of General Psychiatry. 53: 985-9. PMID 8911221 DOI: 10.1001/Archpsyc.1996.01830110021003 |
0.334 |
|
| 1996 |
Kalaydjieva L, Hallmayer J, Chandler D, Savov A, Nikolova A, Angelicheva D, King RH, Ishpekova B, Honeyman K, Calafell F, Shmarov A, Petrova J, Turnev I, Hristova A, Moskov M, et al. Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24. Nature Genetics. 14: 214-7. PMID 8841199 DOI: 10.1038/Ng1096-214 |
0.343 |
|
| 1996 |
Maier W, Minges J, Eckstein N, Brodski C, Albus M, Lerer B, Hallmayer J, Fimmers R, Ackenheil M, Ebstein RE, Borrmann M, Lichtermann D, Wildenauer DB. Genetic relationship between dopamine transporter gene and schizophrenia : linkage and association Schizophrenia Research. 20: 175-180. PMID 8794507 DOI: 10.1016/0920-9964(95)00083-6 |
0.374 |
|
| 1996 |
Hallmayer J, Spiker D, Lotspeich L, McMahon WM, Petersen PB, Nicholas P, Pingree C, Ciaranello RD. Male-to-male transmission in extended pedigrees with multiple cases of autism. American Journal of Medical Genetics. 67: 13-8. PMID 8678108 DOI: 10.1002/(Sici)1096-8628(19960216)67:1<13::Aid-Ajmg2>3.0.Co;2-T |
0.33 |
|
| 1996 |
Wildenauer DB, Hallmayer J, Schwab SG, Albus M, Eckstein GN, Zill P, Hönig S, Strauss M, Borrmann M, Lichtermann D, Ebstein RP, Lerer B, Risch N, Maier W. Searching for susceptibility genes in schizophrenia by genetic linkage analysis. Cold Spring Harbor Symposia On Quantitative Biology. 61: 845-850. DOI: 10.1101/Sqb.1996.061.01.083 |
0.347 |
|
| 1996 |
Wildenauer DB, Hallmayer J, Albus M, Schwab SG, Strauss M, Hoenig S, Borrmann M, Lichtermann D, Ackenheil M, Ebstein RE, Trixler M, Lerer B, Maier W. 18P — A susceptibility locus for affective and schizophrenic disorder? Psychiatric Genetics. 6: 152. DOI: 10.1097/00041444-199623000-00048 |
0.329 |
|
| 1996 |
Maier W, Albus M, Schwab S, Hallmayer J, Ebstein P, Risch N, Lerer B, Wildenauer D. Evaluation of a susceptibility gene for schizophrenia on chromosome 6P Schizophrenia Research. 18: 167. DOI: 10.1016/0920-9964(96)85533-2 |
0.329 |
|
| 1996 |
WiIdenauer DB, Schwab SG, Eckstein G, Hoenig S, Albus M, Hallmayer J, Borrmann M, Lichterrnann D, Fimmers R, Bbstein RP, Lerer B, Risch N, Maier W. A search for schizophrenia genes by affected sib-pair analysis Biological Psychiatry. 39: 614. DOI: 10.1016/0006-3223(96)84331-9 |
0.31 |
|
| 1995 |
Maier W, Hallmayer J, Zill P, Bondy B, Lichtermann D, Ackenheil M, Minges J, Wildenauer D. Linkage analysis between pericentrometric markers on chromosome 18 and bipolar disorder : a replication test Psychiatry Research-Neuroimaging. 59: 7-15. PMID 8771215 DOI: 10.1016/0165-1781(95)02799-8 |
0.393 |
|
| 1995 |
Schwab SG, Lerer B, Albus M, Maier W, Hallmayer J, Fimmers R, Lichtermann D, Minges J, Bondy B, Ackenheil M, Altmark D, Hasib D, Gur E, Ebstein RP, Wildenauer DB. Potential linkage for schizophrenia on chromosome 22q12-q13: A replication study American Journal of Medical Genetics. 60: 436-443. PMID 8546158 DOI: 10.1002/Ajmg.1320600515 |
0.369 |
|
| 1995 |
Bogdanova N, Dworniczak B, Dragova D, Todorov V, Dimitrakov D, Kalinov K, Hallmayer J, Horst J, Kalaydjieva L. Genetic heterogeneity of polycystic kidney disease in Bulgaria. Human Genetics. 95: 645-50. PMID 7789949 DOI: 10.1007/Bf00209481 |
0.364 |
|
| 1995 |
Macaubas C, Hallmayer J, Kalil J, Kimura A, Yasunaga S, Grumet FC, Mignot E. Extensive polymorphism of a (CA)n microsatellite located in the HLA-DQA1/DQB1 class II region. Human Immunology. 42: 209-20. PMID 7759308 DOI: 10.1016/0198-8859(94)00101-U |
0.328 |
|
| 1995 |
Maier W, Schmidt F, Schwab SG, Hallmayer J, Minges J, Ackenheil M, Lichtermann D, Wildenauer DB. Lack of linkage between schizophrenia and markers at the telomeric end of the pseudoautosomal region of the sex chromosomes Biological Psychiatry. 37: 344-347. PMID 7748989 DOI: 10.1016/0006-3223(94)00192-6 |
0.325 |
|
| 1995 |
Schwab SG, Albus M, Hallmayer J, Hönig S, Borrmann M, Lichtermann D, Ebstein RP, Ackenheil M, Lerer B, Risch N. Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis. Nature Genetics. 11: 325-7. PMID 7581458 DOI: 10.1038/Ng1195-325 |
0.405 |
|
| 1994 |
Spiker D, Lotspeich L, Kraemer HC, Hallmayer J, McMahon W, Petersen PB, Nicholas P, Pingree C, Wiese-Slater S, Chiotti C. Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families. American Journal of Medical Genetics. 54: 27-35. PMID 8178836 DOI: 10.1002/Ajmg.1320540107 |
0.338 |
|
| 1994 |
Maier W, Schwab S, Hallmayer J, Ertl MA, Minges J, Ackenheil M, Lichtermann D, Wildenauer D. Absence of linkage between schizophrenia and the dopamine D4 receptor gene. Psychiatry Research-Neuroimaging. 53: 77-86. PMID 7991733 DOI: 10.1016/0165-1781(94)90096-5 |
0.353 |
|
| 1994 |
Barr CL, Kennedy JL, Pakstis AJ, Wetterberg L, Sjögren B, Bierut L, Wadelius C, Wahlström J, Martinsson T, Giuffra L, Gelernter J, Hallmayer J, Moises HW, Kurth J, Cavalli-Sforza LL, et al. Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred American Journal of Medical Genetics. 54: 51-58. PMID 7909991 DOI: 10.1002/Ajmg.1320540110 |
0.336 |
|
| 1994 |
Hallmayer J, Maier W, Schwab S, Ertl MA, Minges J, Ackenheil M, Lichtermann D, Wildenauer DB. No evidence of linkage between the dopamine D2 receptor gene and schizophrenia. Psychiatry Research-Neuroimaging. 53: 203-215. PMID 7824680 DOI: 10.1016/0165-1781(94)90111-2 |
0.312 |
|
| 1993 |
Maier W, Lichtermann D, Minges J, Heun R, Hallmayer J. The impact of gender and age at onset on the familial aggregation of schizophrenia European Archives of Psychiatry and Clinical Neuroscience. 242: 279-285. PMID 8499497 DOI: 10.1007/Bf02190387 |
0.352 |
|
| 1993 |
Maier W, Lichtermann D, Minges J, Hallmayer J, Heun R, Benkert O, Douglas FL. Continuity and Discontinuity of Affective Disorders and Schizophrenia: Results of a Controlled Family Study Archives of General Psychiatry. 50: 871-883. PMID 8215813 DOI: 10.1001/Archpsyc.1993.01820230041004 |
0.36 |
|
| 1993 |
Nöthen MM, Wildenauer D, Cichon S, Schwab S, Kramer R, Hallmayer J, Maier W, Lichtermann D, Minges J, Lanczik M, Rietschel M, Körner J, Ertl MA, Fimmers R, Ackenheil M, et al. No association or linkage between polymorphisms at the porphobilinogen deaminase gene locus and schizophrenia Psychiatric Genetics. 3: 101-106. DOI: 10.1097/00041444-199322000-00006 |
0.347 |
|
| 1992 |
Hallmayer J, Maier W, Ackenheil M, Ertl MA, Schmidt S, Minges J, Lichtermann D, Wildenauer D. Evidence against linkage of schizophrenia to chromosome 5q11-q13 markers in systematically ascertained families. Biological Psychiatry. 31: 83-94. PMID 1543800 DOI: 10.1016/0006-3223(92)90008-N |
0.334 |
|
| 1992 |
Hallmayer J, Kennedy JL, Wetterberg L, Sjögren B, Kidd KK, Cavalli-Sforza LL. Exclusion of linkage between the serotonin2 receptor and schizophrenia in a large Swedish kindred. Archives of General Psychiatry. 49: 216-9. PMID 1348924 DOI: 10.1001/Archpsyc.1992.01820030048006 |
0.344 |
|
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