| Year |
Citation |
Score |
| 2016 |
Hannon E, Dempster E, Viana J, Burrage J, Smith AR, Macdonald R, St Clair D, Mustard C, Breen G, Therman S, Kaprio J, Toulopoulou T, Hulshoff Pol HE, Bohlken MM, Kahn RS, ... ... Gurling H, et al. An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation. Genome Biology. 17: 176. PMID 27572077 DOI: 10.1186/S13059-016-1041-X |
0.327 |
|
| 2015 |
Bigdeli TB, Ripke S, Bacanu SA, Lee SH, Wray NR, Gejman PV, Rietschel M, Cichon S, St Clair D, Corvin A, Kirov G, McQuillin A, Gurling H, Rujescu D, Andreassen OA, et al. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26663532 DOI: 10.1002/Ajmg.B.32402 |
0.314 |
|
| 2015 |
Rajkumar AP, Christensen JH, Mattheisen M, Jacobsen I, Bache I, Pallesen J, Grove J, Qvist P, McQuillin A, Gurling HM, Tümer Z, Mors O, Børglum AD. Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. Bipolar Disorders. 17: 205-11. PMID 25053281 DOI: 10.1111/bdi.12239 |
0.311 |
|
| 2014 |
Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, ... ... Gurling H, et al. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics. 23: 3316-26. PMID 24474471 DOI: 10.1093/Hmg/Ddu025 |
0.32 |
|
| 2014 |
Xu W, Cohen-Woods S, Chen Q, Noor A, Knight J, Hosang G, Parikh SV, De Luca V, Tozzi F, Muglia P, Forte J, McQuillin A, Hu P, Gurling HM, Kennedy JL, et al. Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1. Bmc Medical Genetics. 15: 2. PMID 24387768 DOI: 10.1186/1471-2350-15-2 |
0.319 |
|
| 2013 |
Ruderfer DM, Chambert K, Moran J, Talkowski M, Chen ES, Gigek C, Gusella JF, Blackwood DH, Corvin A, Gurling HM, Hultman CM, Kirov G, Magnusson P, O'Donovan MC, Owen MJ, et al. Mosaic copy number variation in schizophrenia. European Journal of Human Genetics : Ejhg. 21: 1007-11. PMID 23321615 DOI: 10.1038/Ejhg.2012.287 |
0.308 |
|
| 2012 |
Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, ... ... Gurling H, et al. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 28: 377-87. PMID 22027014 DOI: 10.3233/Jad-2011-110824 |
0.372 |
|
| 2012 |
Hollingworth P, Sweet R, Sims R, Harold D, Russo G, Abraham R, Stretton A, Jones N, Gerrish A, Chapman J, Ivanov D, Moskvina V, Lovestone S, Priotsi P, Lupton M, ... ... Gurling H, et al. Genome-wide association study of Alzheimer's disease with psychotic symptoms. Molecular Psychiatry. 17: 1316-27. PMID 22005930 DOI: 10.1016/J.Jalz.2011.05.516 |
0.305 |
|
| 2012 |
Willour VL, Seifuddin F, Mahon PB, Jancic D, Pirooznia M, Steele J, Schweizer B, Goes FS, Mondimore FM, Mackinnon DF, Perlis RH, Lee PH, Huang J, Kelsoe JR, ... ... Gurling H, et al. A genome-wide association study of attempted suicide. Molecular Psychiatry. 17: 433-44. PMID 21423239 DOI: 10.1038/Mp.2011.4 |
0.348 |
|
| 2011 |
Hamshere ML, O'Donovan MC, Jones IR, Jones L, Kirov G, Green EK, Moskvina V, Grozeva D, Bass N, McQuillin A, Gurling H, St Clair D, Young AH, Ferrier IN, Farmer A, et al. Polygenic dissection of the bipolar phenotype. The British Journal of Psychiatry : the Journal of Mental Science. 198: 284-8. PMID 21972277 DOI: 10.1192/Bjp.Bp.110.087866 |
0.418 |
|
| 2011 |
Ingason A, Kirov G, Giegling I, Hansen T, Isles AR, Jakobsen KD, Kristinsson KT, le Roux L, Gustafsson O, Craddock N, Möller HJ, McQuillin A, Muglia P, Cichon S, Rietschel M, ... ... Gurling H, et al. Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness. The American Journal of Psychiatry. 168: 408-17. PMID 21324950 DOI: 10.1176/Appi.Ajp.2010.09111660 |
0.391 |
|
| 2011 |
McQuillin A, Bass N, Anjorin A, Lawrence J, Kandaswamy R, Lydall G, Moran J, Sklar P, Purcell S, Gurling H. Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample. European Journal of Human Genetics : Ejhg. 19: 588-92. PMID 21206513 DOI: 10.1038/ejhg.2010.221 |
0.318 |
|
| 2011 |
Mahon PB, Pirooznia M, Goes FS, Seifuddin F, Steele J, Lee PH, Huang J, Hamshere ML, Depaulo JR, Kelsoe JR, Rietschel M, Nöthen M, Cichon S, Gurling H, Purcell S, et al. Erratum to “Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder”, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics”, April 1; 156(3):370–378 American Journal of Medical Genetics. 156: 749-750. DOI: 10.1002/Ajmg.B.31228 |
0.307 |
|
| 2010 |
Perlis RH, Huang J, Purcell S, Fava M, Rush AJ, Sullivan PF, Hamilton SP, McMahon FJ, Schulze TG, Schulze T, Potash JB, Zandi PP, Willour VL, Penninx BW, Boomsma DI, ... ... Gurling H, et al. Genome-wide association study of suicide attempts in mood disorder patients. The American Journal of Psychiatry. 167: 1499-507. PMID 21041247 DOI: 10.1176/Appi.Ajp.2010.10040541 |
0.374 |
|
| 2010 |
Mathieu F, Dizier MH, Etain B, Jamain S, Rietschel M, Maier W, Albus M, McKeon P, Roche S, Blackwood D, Muir WJ, Henry C, Malafosse A, Preisig M, Ferrero F, ... ... Gurling H, et al. European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 1425-33. PMID 20886542 DOI: 10.1002/ajmg.b.31121 |
0.313 |
|
| 2010 |
Nyegaard M, Severinsen JE, Als TD, Hedemand A, Straarup S, Nordentoft M, McQuillin A, Bass N, Lawrence J, Thirumalai S, Pereira AC, Kandaswamy R, Lydall GJ, Sklar P, Scolnick E, ... ... Gurling HM, et al. Support of association between BRD1 and both schizophrenia and bipolar affective disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 582-91. PMID 19693800 DOI: 10.1002/ajmg.b.31023 |
0.319 |
|
| 2010 |
Yan TC, McQuillin A, Thapar A, Asherson P, Hunt SP, Stanford SC, Gurling H. NK1 (TACR1) receptor gene 'knockout' mouse phenotype predicts genetic association with ADHD. Journal of Psychopharmacology (Oxford, England). 24: 27-38. PMID 19204064 DOI: 10.1177/0269881108100255 |
0.313 |
|
| 2010 |
Datta SR, McQuillin A, Rizig M, Blaveri E, Thirumalai S, Kalsi G, Lawrence J, Bass NJ, Puri V, Choudhury K, Pimm J, Crombie C, Fraser G, Walker N, Curtis D, ... ... Gurling HM, et al. A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular Psychiatry. 15: 615-28. PMID 19048012 DOI: 10.1038/mp.2008.128 |
0.31 |
|
| 2009 |
Bass NJ, Datta SR, McQuillin A, Puri V, Choudhury K, Thirumalai S, Lawrence J, Quested D, Pimm J, Curtis D, Gurling HM. Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia. Behavioral and Brain Functions : Bbf. 5: 28. PMID 19586533 DOI: 10.1186/1744-9081-5-28 |
0.358 |
|
| 2009 |
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Ruderfer DM, McQuillin A, Morris DW, Oĝdushlaine CT, Corvin A, Holmans PA, Oĝdonovan MC, MacGregor S, Gurling H, et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Nature. 460: 748-752. PMID 19571811 DOI: 10.1038/Nature08185 |
0.426 |
|
| 2009 |
Vine AE, McQuillin A, Bass NJ, Pereira A, Kandaswamy R, Robinson M, Lawrence J, Anjorin A, Sklar P, Gurling HM, Curtis D. No evidence for excess runs of homozygosity in bipolar disorder. Psychiatric Genetics. 19: 165-70. PMID 19451863 DOI: 10.1097/YPG.0b013e32832a4faa |
0.319 |
|
| 2009 |
Perlis RH, Smoller JW, Ferreira MA, McQuillin A, Bass N, Lawrence J, Sachs GS, Nimgaonkar V, Scolnick EM, Gurling H, Sklar P, Purcell S. A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder. The American Journal of Psychiatry. 166: 718-25. PMID 19448189 DOI: 10.1176/Appi.Ajp.2009.08111633 |
0.344 |
|
| 2009 |
Hennah W, Thomson P, McQuillin A, Bass N, Loukola A, Anjorin A, Blackwood D, Curtis D, Deary IJ, Harris SE, Isometsä ET, Lawrence J, Lönnqvist J, Muir W, Palotie A, ... ... Gurling H, et al. DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder. Molecular Psychiatry. 14: 865-73. PMID 18317464 DOI: 10.1038/mp.2008.22 |
0.405 |
|
| 2009 |
McQuillin A, Bass NJ, Choudhury K, Puri V, Kosmin M, Lawrence J, Curtis D, Gurling HM. Case-control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipolar-affective disorders. Molecular Psychiatry. 14: 614-20. PMID 18268501 DOI: 10.1038/mp.2008.6 |
0.302 |
|
| 2008 |
Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, et al. Rare chromosomal deletions and duplications increase risk of schizophrenia Nature. 455: 237-241. PMID 18668038 DOI: 10.1038/Nature07239 |
0.351 |
|
| 2008 |
Puri V, McQuillin A, Datta S, Choudhury K, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Walker N, Moorey H, Ray MK, ... ... Gurling H, et al. Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3. European Journal of Human Genetics : Ejhg. 16: 1275-82. PMID 18414510 DOI: 10.1038/ejhg.2008.76 |
0.33 |
|
| 2007 |
Datta SR, McQuillin A, Puri V, Choudhury K, Thirumalai S, Lawrence J, Pimm J, Bass N, Lamb G, Moorey H, Morgan J, Punukollu B, Kandasami G, Kirwin S, Sule A, ... ... Gurling HM, et al. Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia. Behavioral and Brain Functions : Bbf. 3: 50. PMID 17888175 DOI: 10.1186/1744-9081-3-50 |
0.325 |
|
| 2007 |
Choudhury K, McQuillin A, Puri V, Pimm J, Datta S, Thirumalai S, Krasucki R, Lawrence J, Bass NJ, Quested D, Crombie C, Fraser G, Walker N, Nadeem H, Johnson S, ... ... Gurling HM, et al. A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia. American Journal of Human Genetics. 80: 664-72. PMID 17357072 DOI: 10.1086/513475 |
0.326 |
|
| 2007 |
Gurling H, Pimm J, McQuillin A. Replication of genetic association studies between markers at the Epsin 4 gene locus and schizophrenia in two Han Chinese samples. Schizophrenia Research. 89: 357-9. PMID 17070672 DOI: 10.1016/j.schres.2006.08.024 |
0.324 |
|
| 2007 |
Puri V, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Moorey H, Morgan J, Punukollu B, Kandasami G, Curtis D, ... Gurling H, et al. Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene. Biological Psychiatry. 61: 873-9. PMID 16978587 DOI: 10.1016/j.biopsych.2006.06.014 |
0.334 |
|
| 2006 |
Kalsi G, McQuillin A, Degn B, Lundorf MD, Bass NJ, Lawrence J, Choudhury K, Puri V, Nyegaard M, Curtis D, Mors O, Kruse T, Kerwin S, Gurling H. Identification of the Slynar gene (AY070435) and related brain expressed sequences as a candidate gene for susceptibility to affective disorders through allelic and haplotypic association with bipolar disorder on chromosome 12q24. The American Journal of Psychiatry. 163: 1767-76. PMID 17012688 DOI: 10.1176/appi.ajp.163.10.1767 |
0.422 |
|
| 2006 |
Gurling HM, Critchley H, Datta SR, McQuillin A, Blaveri E, Thirumalai S, Pimm J, Krasucki R, Kalsi G, Quested D, Lawrence J, Bass N, Choudhury K, Puri V, O'Daly O, et al. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. Archives of General Psychiatry. 63: 844-54. PMID 16894060 DOI: 10.1001/archpsyc.63.8.844 |
0.36 |
|
| 2006 |
Etain B, Mathieu F, Rietschel M, Maier W, Albus M, McKeon P, Roche S, Kealey C, Blackwood D, Muir W, Bellivier F, Henry C, Dina C, Gallina S, Gurling H, et al. Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14. Molecular Psychiatry. 11: 685-94. PMID 16534504 DOI: 10.1038/Sj.Mp.4001815 |
0.39 |
|
| 2006 |
Rizig MA, McQuillin A, Puri V, Choudhury K, Datta S, Thirumalai S, Lawrence J, Quested D, Pimm J, Bass N, Lamb G, Moorey H, Badacsonyi A, Kelly K, Morgan J, ... ... Gurling H, et al. Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 296-300. PMID 16508931 DOI: 10.1002/ajmg.b.30288 |
0.363 |
|
| 2006 |
McQuillin A, Bass NJ, Kalsi G, Lawrence J, Puri V, Choudhury K, Detera-Wadleigh SD, Curtis D, Gurling HM. Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3. Molecular Psychiatry. 11: 134-42. PMID 16205735 DOI: 10.1038/sj.mp.4001759 |
0.305 |
|
| 2006 |
Puri V, McQuillin A, Thirumalai S, Lawrence J, Krasucki R, Choudhury K, Datta S, Kerwin S, Quested D, Bass N, Pimm J, Lamb G, Moorey H, Kandasami G, Badacsonyi A, ... ... Gurling HM, et al. Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sample. Biological Psychiatry. 59: 195-7. PMID 16202394 DOI: 10.1016/j.biopsych.2005.08.015 |
0.346 |
|
| 2005 |
Pimm J, McQuillin A, Thirumalai S, Lawrence J, Quested D, Bass N, Lamb G, Moorey H, Datta SR, Kalsi G, Badacsonyi A, Kelly K, Morgan J, Punukollu B, Curtis D, ... Gurling H, et al. The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia. American Journal of Human Genetics. 76: 902-7. PMID 15793701 DOI: 10.1086/430095 |
0.348 |
|
| 2004 |
Buttenschön HN, Mors O, Ewald H, McQuillin A, Kalsi G, Lawrence J, Gurling H, Kruse TA. No association between a neuronal nitric oxide synthase (NOS1) gene polymorphism on chromosome 12q24 and bipolar disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 124: 73-5. PMID 14681919 DOI: 10.1002/ajmg.b.20040 |
0.352 |
|
| 2003 |
Carbonell J, Allen R, Kalsi G, McQuillin A, Livingston G, Katona C, Walker Z, Katz A, Rands G, Stevens T, Crossan I, Curtis D, Gurling H. Variation in the DCP1 gene, encoding the angiotensin converting enzyme ACE, is not associated with increased susceptibility to Alzheimer's disease. Psychiatric Genetics. 13: 47-50. PMID 12605101 DOI: 10.1097/01.ypg.0000054711.85338.5c |
0.327 |
|
| 2002 |
McQuillin A, Kalsi G, Moorey H, Lamb G, Mayet S, Quested D, Baker P, Curtis D, Gurling HM. A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia. European Journal of Human Genetics : Ejhg. 10: 491-4. PMID 12111645 DOI: 10.1038/sj.ejhg.5200837 |
0.337 |
|
| 2001 |
Gurling H, Chen AC. Gene expression in schizophrenia. The American Journal of Psychiatry. 158: 1740-1. PMID 11579022 DOI: 10.1176/appi.ajp.158.10.1740 |
0.358 |
|
| 2001 |
Blaveri E, Kalsi G, Lawrence J, Quested D, Moorey H, Lamb G, Kohen D, Shiwach R, Chowdhury U, Curtis D, McQuillin A, Gramoustianou ES, Gurling HM. Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1). European Journal of Human Genetics : Ejhg. 9: 469-72. PMID 11436130 DOI: 10.1038/sj.ejhg.5200646 |
0.325 |
|
| 2001 |
Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D. Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. American Journal of Human Genetics. 68: 661-73. PMID 11179014 DOI: 10.1086/318788 |
0.3 |
|
| 2000 |
Blaveri E, Kalsi G, McGuililn A, Read T, Murphy P, Curtis, Gurling H. Genetic linkage analysis of schizophrenia and schizophrenia specture disorders on chromosome 8P21-22 in a New British family sample American Journal of Medical Genetics - Neuropsychiatric Genetics. 96: 460-461. |
0.364 |
|
| 2000 |
Gurling HMD, Curtis D, Kalsi G, McQuillin A, Lawrence J, Murphy P, Brynjolfsson J, McInnis M, Sigmundsson T, Petursson H. Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia American Journal of Medical Genetics - Neuropsychiatric Genetics. 96: 460. |
0.308 |
|
| 1999 |
Kalsi G, Mankoo B, Curtis D, Sherrington R, Melmer G, Brynjolfsson J, Sigmundsson T, Read T, Murphy P, Petursson H, Gurling H. New DNA markers with increased informativeness show diminished support for a chromosome 5q11-13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families. Annals of Human Genetics. 63: 235-47. PMID 10738536 DOI: 10.1017/S0003480099007502 |
0.401 |
|
| 1999 |
Kalsi G, Gamble D, Curtis D, Brynjolfsson J, Sigmundsson T, Butler R, Read T, Murphy P, Petursson H, Gurling HM. No evidence for linkage of schizophrenia to DXS7 at chromosome Xp11. Psychiatric Genetics. 9: 197-9. PMID 10697827 |
0.335 |
|
| 1999 |
McQuillin A, Lawrence J, Curtis D, Kalsi G, Smyth C, Hannesdottir S, Gurling H. Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder. Psychological Medicine. 29: 1449-54. PMID 10616951 DOI: 10.1017/S0033291799001166 |
0.43 |
|
| 1999 |
McQuillin A, Lawrence J, Kalsi G, Chen A, Gurling H, Curtis D. No allelic association between bipolar affective disorder and the tryptophan hydroxylase gene. Archives of General Psychiatry. 56: 99-101. PMID 9892263 DOI: 10.1001/archpsyc.56.1.99 |
0.375 |
|
| 1998 |
Vincent JB, Kalsi G, Klempan T, Tatuch Y, Sherrington RP, Breschel T, McInnis MG, Brynjolfsson J, Petursson H, Gurling HM, Gottesman II, Torrey EF, Petronis A, Kennedy JL. No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins. Human Genetics. 103: 41-7. PMID 9737774 DOI: 10.1007/S004390050780 |
0.307 |
|
| 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, ... ... Gurling H, 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 |
0.447 |
|
| 1998 |
Williams J, Spurlock G, Holmans P, Mant R, Murphy K, Jones L, Cardno A, Asherson P, Blackwood D, Muir W, Meszaros K, Aschauer H, Mallet J, Laurent C, Pekkarinen P, ... ... Gurling H, et al. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry. 3: 141-9. PMID 9577838 DOI: 10.1038/Sj.Mp.4000376 |
0.404 |
|
| 1997 |
Smyth C, Kalsi G, Brynjolfsson J, O'Neill J, Curtis D, Rifkin L, Moloney E, Murphy P, Petursson H, Gurling H. Test of Xq26.3-28 linkage in bipolar and unipolar affective disorder in families selected for absence of male to male transmission. The British Journal of Psychiatry : the Journal of Mental Science. 171: 578-81. PMID 9519101 DOI: 10.1192/Bjp.171.6.578 |
0.397 |
|
| 1997 |
Sharma T, du Boulay G, Lewis S, Sigmundsson T, Gurling H, Murray R. The Maudsley Family Study. I: Structural brain changes on magnetic resonance imaging in familial schizophrenia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 21: 1297-315. PMID 9460093 DOI: 10.1016/S0278-5846(97)00165-6 |
0.346 |
|
| 1997 |
Goldin LR, Gershon ES, Berrettini WH, Stine OC, DePaulo R, McMahon F, Meyers D, Nothen M, Propping P, Cichon S, Fimmers R, Baur M, Albus M, Franzek E, Kreiner R, ... ... Gurling H, et al. Description of the Genetic Analysis Workshop 10 bipolar disorder linkage data sets. Genetic Epidemiology. 14: 563-8. PMID 9433543 DOI: 10.1002/(Sici)1098-2272(1997)14:6<563::Aid-Gepi2>3.0.Co;2-0 |
0.352 |
|
| 1997 |
Chen AC, Kalsi G, Brynjolfsson J, Sigmundsson T, Curtis D, Butler R, Read T, Murphy P, Barnard EA, Petursson H, Gurling HM. Exclusion of linkage between schizophrenia and the gene encoding a neutral amino acid glutamate/aspartate transporter, SLC1A5. American Journal of Medical Genetics. 74: 50-2. PMID 9034006 DOI: 10.1002/(SICI)1096-8628(19970221)74:1<50::AID-AJMG11>3.0.CO;2-Q |
0.324 |
|
| 1997 |
Sharma T, Lewis S, Sigmundsson T, Lancaster E, Barta P, Pearlson G, Gurling H, Murray R. Loss of cerebral asymmetry in familial schizophrenia — a volumetric study using unbiased stereology Psychiatry Research: Neuroimaging. 68: 177-178. DOI: 10.1016/S0925-4927(97)81578-8 |
0.37 |
|
| 1996 |
Chen AC, Kalsi G, Brynjolfsson J, Sigmundsson T, Curtis D, Butler R, Read T, Murphy P, Petursson H, Barnard EA, Gurling HM. Lack of evidence for close linkage of the glutamate GluR6 receptor gene with schizophrenia. The American Journal of Psychiatry. 153: 1634-6. PMID 8942465 |
0.321 |
|
| 1996 |
Smyth C, Kalsi G, Brynjolfsson J, O'Neill J, Curtis D, Rifkin L, Moloney E, Murphy P, Sherrington R, Petursson H, Gurling H. Further tests for linkage of bipolar affective disorder to the tyrosine hydroxylase gene locus on chromosome 11p15 in a new series of multiplex British affective disorder pedigrees. The American Journal of Psychiatry. 153: 271-4. PMID 8561212 DOI: 10.1176/Ajp.153.2.271 |
0.425 |
|
| 1996 |
Gurling H, Kalsi G, Chen A, Green M, Butler R, Read T, Murphy P, Curtis D, Sharma T. Erratum: Schizophrenia susceptibility and chromosome 6p24-22 (vol 11, pg 234, 1995) Nature Genetics. 13: 129-129. DOI: 10.1038/Ng0596-129B |
0.39 |
|
| 1996 |
Sharma T, Lewis S, Sigmundsson T, Lancaster E, Barta P, Pearlson G, Gurling H, Murray R. Loss of cerebral asymmetry in familial schizophrenia — A volumetric study using unbiased stereology European Neuropsychopharmacology. 6: 181. DOI: 10.1016/0924-977X(96)88148-X |
0.37 |
|
| 1996 |
Sharma T, Sigmundsson T, Lewis S, Lancaster E, Barta P, Pearlson G, Gurling H, Murray R. Loss of developmental torque in familial schizophrenia — A volumetric magnetic resonance imaging study using unbiased stereology European Psychiatry. 11: 229s. DOI: 10.1016/0924-9338(96)88682-2 |
0.333 |
|
| 1996 |
Sharma T, Lewis S, Sigmundsson T, Lancaster E, Pearlson G, Gurling H, Murray R. Loss of cerebral asymmetry in familial schizophrenia, a volumetric study using unbiased stereology Biological Psychiatry. 39: 602. DOI: 10.1016/0006-3223(96)84290-9 |
0.369 |
|
| 1995 |
Kalsi G, Curtis D, Brynjolfsson J, Butler R, Sharma T, Murphy P, Read T, Petursson H, Gurling HM. Investigation by linkage analysis of the XY pseudoautosomal region in the genetic susceptibility to schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 167: 390-3. PMID 7496650 |
0.319 |
|
| 1994 |
Sherrington R, Curtis D, Brynjolfsson J, Moloney E, Rifkin L, Petursson H, Gurling H. A linkage study of affective disorder with DNA markers for the ABO-AK1-ORM linkage group near the dopamine beta hydroxylase gene. Biological Psychiatry. 36: 434-42. PMID 7811839 DOI: 10.1016/0006-3223(94)90638-6 |
0.399 |
|
| 1994 |
Kalsi G, Mankoo BS, Brynjolfsson J, Curtis D, Read T, Murphy P, Sharma T, Petursson H, Gurling HM. The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia. Psychiatric Genetics. 4: 219-27. PMID 7712119 |
0.301 |
|
| 1993 |
Sherrington R, Mankoo B, Dixon M, Curtis D, Kalsi G, Melmer G, Gurling H. Microsatellite polymorphisms for chromosome 5 bands q11.2-q13.3. Human Heredity. 43: 197-202. PMID 8330884 DOI: 10.1159/000154177 |
0.336 |
|
| 1993 |
Sherrington R, Mankoo B, Attwood J, Kalsi G, Curtis D, Buetow K, Povey S, Gurling H. Cloning of the human dopamine D5 receptor gene and identification of a highly polymorphic microsatellite for the DRD5 locus that shows tight linkage to the chromosome 4p reference marker RAF1P1. Genomics. 18: 423-5. PMID 8288248 DOI: 10.1006/geno.1993.1489 |
0.316 |
|
| 1993 |
Melki J, Burlet P, Clermont O, Pascal F, Paul B, Abdelhak S, Sherrington R, Gurling H, Nakamura Y, Weissenbach J. Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy gene. Genomics. 15: 521-4. PMID 8096827 DOI: 10.1006/Geno.1993.1103 |
0.328 |
|
| 1993 |
Lim LC, Gurling H, Curtis D, Brynjolfsson J, Petursson H, Gill M. Linkage between tyrosine hydroxylase gene and affective disorder cannot be excluded in two of six pedigrees. American Journal of Medical Genetics. 48: 223-8. PMID 7907843 DOI: 10.1002/Ajmg.1320480410 |
0.306 |
|
| 1993 |
Sharma T, Brynjolfsson J, Butler R, Read T, Murphy P, Sigmundsson T, Petursson H, Gurling H. Genomic imprinting in the Icelandic/ British schizophrenia study: Preliminary results Schizophrenia Research. 9: 124-125. DOI: 10.1016/0920-9964(93)90191-K |
0.369 |
|
| 1993 |
Brynjolfsson J, Sharma T, Butler R, Read T, Murphy P, Sigmundsson T, Petursson H, Gurling H. Age of onset in familial schizophrenia: Icelandic/British study Schizophrenia Research. 9: 115. DOI: 10.1016/0920-9964(93)90160-K |
0.369 |
|
| 1992 |
Sharma T, Lewis SW, Ron MA, Moloney E, Gurling H. The search for an endophenotype correlated with a subtype of schizophrenia: Magnetic resonance imaging in two large British Pedigrees Schizophrenia Research. 6: 96-97. DOI: 10.1016/0920-9964(92)90101-A |
0.314 |
|
| 1991 |
Holmes D, Brynjolfsson J, Brett P, Curtis D, Petursson H, Sherrington R, Gurling H. No evidence for a susceptibility locus predisposing to manic depression in the region of the dopamine (D2) receptor gene. The British Journal of Psychiatry : the Journal of Mental Science. 158: 635-41. PMID 1677600 DOI: 10.1192/Bjp.158.5.635 |
0.335 |
|
| 1991 |
Gurling H, Sharma T. Molecular genetic research in schizophrenia The Psychiatrist. 15: 512-512. DOI: 10.1192/Pb.15.8.512 |
0.375 |
|
| 1991 |
Gurling H, Nurnberger J. Psychiatric genetics 2nd world congress abstracts editorial introduction Psychiatric Genetics. 1: i-ii. DOI: 10.1097/00041444-199102010-00001 |
0.309 |
|
| 1990 |
Curtis D, Gurling H. Unsound methodology in investigating a pseudoautosomal locus in schizophrenia. The British Journal of Psychiatry : the Journal of Mental Science. 156: 415-6. PMID 2346843 DOI: 10.1192/Bjp.156.3.415 |
0.38 |
|
| 1990 |
Gurling H. Genetic linkage and psychiatric disease. Nature. 344: 298-9. PMID 2314467 DOI: 10.1038/344298a0 |
0.328 |
|
| 1989 |
Detera-Wadleigh SD, Goldin LR, Sherrington R, Encio I, de Miguel C, Berrettini W, Gurling H, Gershon ES. Exclusion of linkage to 5q11-13 in families with schizophrenia and other psychiatric disorders. Nature. 340: 391-3. PMID 2755489 DOI: 10.1038/340391a0 |
0.464 |
|
| 1989 |
Gurling H. Genetics of schizophrenia. Lancet. 1: 277. PMID 2563436 DOI: 10.1016/S0140-6736(89)91284-1 |
0.39 |
|
| 1988 |
Sherrington R, Brynjolfsson J, Petursson H, Potter M, Dudleston K, Barraclough B, Wasmuth J, Dobbs M, Gurling H. Localization of a susceptibility locus for schizophrenia on chromosome 5. Nature. 336: 164-7. PMID 2903449 DOI: 10.1038/336164a0 |
0.462 |
|
| 1987 |
Hodgkinson S, Sherrington R, Gurling H, Marchbanks R, Reeders S, Mallet J, McInnis M, Petursson H, Brynjolfsson J. Molecular genetic evidence for heterogeneity in manic depression. Nature. 325: 805-6. PMID 2881210 DOI: 10.1038/325805a0 |
0.323 |
|
| 1985 |
Feder J, Gurling HM, Darby J, Cavalli-Sforza LL. DNA restriction fragment analysis of the proopiomelanocortin gene in schizophrenia and bipolar disorders. American Journal of Human Genetics. 37: 286-94. PMID 2984925 |
0.302 |
|
| Show low-probability matches. |