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Items: 1 to 50 of 59

1.

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.

Yilmaz Z, Szatkiewicz JP, Crowley JJ, Ancalade N, Brandys MK, van Elburg A, de Kovel CGF, Adan RAH, Hinney A, Hebebrand J, Gratacos M, Fernandez-Aranda F, Escaramis G, Gonzalez JR, Estivill X; Genetic Consortium for Anorexia Nervosa, Wellcome Trust Case Control Consortium 3, Zeggini E, Sullivan PF, Bulik CM.

Psychiatr Genet. 2017 Aug;27(4):152-158. doi: 10.1097/YPG.0000000000000172.

PMID:
28368970
2.

Prenatal exposure to mixtures of xenoestrogens and genome-wide DNA methylation in human placenta.

Vilahur N, Bustamante M, Morales E, Motta V, Fernandez MF, Salas LA, Escaramis G, Ballester F, Murcia M, Tardon A, Riaño I, Santa-Marina L, Ibarluzea J, Arrebola JP, Estivill X, Bollati V, Sunyer J, Olea N.

Epigenomics. 2016 Jan;8(1):43-54. doi: 10.2217/epi.15.91. Epub 2015 Dec 18.

PMID:
26679211
3.

Specific small-RNA signatures in the amygdala at premotor and motor stages of Parkinson's disease revealed by deep sequencing analysis.

Pantano L, Friedländer MR, Escaramís G, Lizano E, Pallarès-Albanell J, Ferrer I, Estivill X, Martí E.

Bioinformatics. 2016 Mar 1;32(5):673-81. doi: 10.1093/bioinformatics/btv632. Epub 2015 Nov 2.

PMID:
26530722
4.

A decade of structural variants: description, history and methods to detect structural variation.

Escaramís G, Docampo E, Rabionet R.

Brief Funct Genomics. 2015 Sep;14(5):305-14. doi: 10.1093/bfgp/elv014. Epub 2015 Apr 15. Review.

PMID:
25877305
5.

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

Bassaganyas L, Beà S, Escaramís G, Tornador C, Salaverria I, Zapata L, Drechsel O, Ferreira PG, Rodriguez-Santiago B, Tubio JM, Navarro A, Martín-García D, López C, Martínez-Trillos A, López-Guillermo A, Gut M, Ossowski S, López-Otín C, Campo E, Estivill X.

Leukemia. 2015 Mar;29(3):758. doi: 10.1038/leu.2014.309. No abstract available.

6.

Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system.

Docampo E, Escaramís G, Gratacòs M, Villatoro S, Puig A, Kogevinas M, Collado A, Carbonell J, Rivera J, Vidal J, Alegre J, Estivill X, Rabionet R.

Pain. 2014 Jun;155(6):1102-9. doi: 10.1016/j.pain.2014.02.016. Epub 2014 Feb 26.

PMID:
24582949
7.

A genome-wide association study of anorexia nervosa.

Boraska V, Franklin CS, Floyd JA, Thornton LM, Huckins LM, Southam L, Rayner NW, Tachmazidou I, Klump KL, Treasure J, Lewis CM, Schmidt U, Tozzi F, Kiezebrink K, Hebebrand J, Gorwood P, Adan RA, Kas MJ, Favaro A, Santonastaso P, Fernández-Aranda F, Gratacos M, Rybakowski F, Dmitrzak-Weglarz M, Kaprio J, Keski-Rahkonen A, Raevuori A, Van Furth EF, Slof-Op 't Landt MC, Hudson JI, Reichborn-Kjennerud T, Knudsen GP, Monteleone P, Kaplan AS, Karwautz A, Hakonarson H, Berrettini WH, Guo Y, Li D, Schork NJ, Komaki G, Ando T, Inoko H, Esko T, Fischer K, Männik K, Metspalu A, Baker JH, Cone RD, Dackor J, DeSocio JE, Hilliard CE, O'Toole JK, Pantel J, Szatkiewicz JP, Taico C, Zerwas S, Trace SE, Davis OS, Helder S, Bühren K, Burghardt R, de Zwaan M, Egberts K, Ehrlich S, Herpertz-Dahlmann B, Herzog W, Imgart H, Scherag A, Scherag S, Zipfel S, Boni C, Ramoz N, Versini A, Brandys MK, Danner UN, de Kovel C, Hendriks J, Koeleman BP, Ophoff RA, Strengman E, van Elburg AA, Bruson A, Clementi M, Degortes D, Forzan M, Tenconi E, Docampo E, Escaramís G, Jiménez-Murcia S, Lissowska J, Rajewski A, Szeszenia-Dabrowska N, Slopien A, Hauser J, Karhunen L, Meulenbelt I, Slagboom PE, Tortorella A, Maj M, Dedoussis G, Dikeos D, Gonidakis F, Tziouvas K, Tsitsika A, Papezova H, Slachtova L, Martaskova D, Kennedy JL, Levitan RD, Yilmaz Z, Huemer J, Koubek D, Merl E, Wagner G, Lichtenstein P, Breen G, Cohen-Woods S, Farmer A, McGuffin P, Cichon S, Giegling I, Herms S, Rujescu D, Schreiber S, Wichmann HE, Dina C, Sladek R, Gambaro G, Soranzo N, Julia A, Marsal S, Rabionet R, Gaborieau V, Dick DM, Palotie A, Ripatti S, Widén E, Andreassen OA, Espeseth T, Lundervold A, Reinvang I, Steen VM, Le Hellard S, Mattingsdal M, Ntalla I, Bencko V, Foretova L, Janout V, Navratilova M, Gallinger S, Pinto D, Scherer SW, Aschauer H, Carlberg L, Schosser A, Alfredsson L, Ding B, Klareskog L, Padyukov L, Courtet P, Guillaume S, Jaussent I, Finan C, Kalsi G, Roberts M, Logan DW, Peltonen L, Ritchie GR, Barrett JC; Wellcome Trust Case Control Consortium 3, Estivill X, Hinney A, Sullivan PF, Collier DA, Zeggini E, Bulik CM.

Mol Psychiatry. 2014 Oct;19(10):1085-94. doi: 10.1038/mp.2013.187. Epub 2014 Feb 11.

8.

ALDH5A1 variability in opioid dependent patients could influence response to methadone treatment.

Fonseca F, Gratacòs M, Escaramís G, De Cid R, Martín-Santos R, Farré M, Estivill X, Torrens M.

Eur Neuropsychopharmacol. 2014 Mar;24(3):420-4. doi: 10.1016/j.euroneuro.2013.10.003. Epub 2013 Oct 18.

PMID:
24230997
9.

Cluster analysis of clinical data identifies fibromyalgia subgroups.

Docampo E, Collado A, Escaramís G, Carbonell J, Rivera J, Vidal J, Alegre J, Rabionet R, Estivill X.

PLoS One. 2013 Sep 30;8(9):e74873. doi: 10.1371/journal.pone.0074873. eCollection 2013.

10.

Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencing.

Trujillano D, Perez B, González J, Tornador C, Navarrete R, Escaramis G, Ossowski S, Armengol L, Cornejo V, Desviat LR, Ugarte M, Estivill X.

Eur J Hum Genet. 2014 Apr;22(4):528-34. doi: 10.1038/ejhg.2013.175. Epub 2013 Aug 14.

11.

Distinguishability and agreement with continuous data.

Carrasco JL, Caceres A, Escaramis G, Jover L.

Stat Med. 2014 Jan 15;33(1):117-28. doi: 10.1002/sim.5896. Epub 2013 Jul 3.

PMID:
23825013
12.

PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data.

Escaramís G, Tornador C, Bassaganyas L, Rabionet R, Tubio JM, Martínez-Fundichely A, Cáceres M, Gut M, Ossowski S, Estivill X.

PLoS One. 2013 May 21;8(5):e63377. doi: 10.1371/journal.pone.0063377. Print 2013.

13.

Next generation diagnostics of cystic fibrosis and CFTR-related disorders by targeted multiplex high-coverage resequencing of CFTR.

Trujillano D, Ramos MD, González J, Tornador C, Sotillo F, Escaramis G, Ossowski S, Armengol L, Casals T, Estivill X.

J Med Genet. 2013 Jul;50(7):455-62. doi: 10.1136/jmedgenet-2013-101602. Epub 2013 May 17.

PMID:
23687349
14.

Upregulation of a small vault RNA (svtRNA2-1a) is an early event in Parkinson disease and induces neuronal dysfunction.

Miñones-Moyano E, Friedländer MR, Pallares J, Kagerbauer B, Porta S, Escaramís G, Ferrer I, Estivill X, Martí E.

RNA Biol. 2013 Jul;10(7):1093-106. doi: 10.4161/rna.24813. Epub 2013 May 1.

15.

Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis.

Bassaganyas L, Beà S, Escaramís G, Tornador C, Salaverria I, Zapata L, Drechsel O, Ferreira PG, Rodriguez-Santiago B, Tubio JM, Navarro A, Martín-García D, López C, Martínez-Trillos A, López-Guillermo A, Gut M, Ossowski S, López-Otín C, Campo E, Estivill X.

Leukemia. 2013 Dec;27(12):2376-9. doi: 10.1038/leu.2013.127. Epub 2013 Apr 24. No abstract available. Erratum in: Leukemia. 2015 Mar;29(3):758.

16.

Interaction of SLC1A1 gene variants and life stress on pharmacological resistance in obsessive-compulsive disorder.

Real E, Gratacòs M, Labad J, Alonso P, Escaramís G, Segalàs C, Subirà M, López-Solà C, Estivill X, Menchón JM.

Pharmacogenomics J. 2013 Oct;13(5):470-5. doi: 10.1038/tpj.2012.30. Epub 2012 Jul 10.

PMID:
22776887
17.

Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder.

Alonso P, Gratacós M, Segalàs C, Escaramís G, Real E, Bayés M, Labad J, López-Solà C, Estivill X, Menchón JM.

J Psychiatry Neurosci. 2012 Jul;37(4):273-81. doi: 10.1503/jpn.110109.

18.

DNA hypomethylation at ALOX12 is associated with persistent wheezing in childhood.

Morales E, Bustamante M, Vilahur N, Escaramis G, Montfort M, de Cid R, Garcia-Esteban R, Torrent M, Estivill X, Grimalt JO, Sunyer J.

Am J Respir Crit Care Med. 2012 May 1;185(9):937-43. doi: 10.1164/rccm.201105-0870OC. Epub 2012 Feb 9.

PMID:
22323304
19.

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia.

Puente XS, Pinyol M, Quesada V, Conde L, Ordóñez GR, Villamor N, Escaramis G, Jares P, Beà S, González-Díaz M, Bassaganyas L, Baumann T, Juan M, López-Guerra M, Colomer D, Tubío JM, López C, Navarro A, Tornador C, Aymerich M, Rozman M, Hernández JM, Puente DA, Freije JM, Velasco G, Gutiérrez-Fernández A, Costa D, Carrió A, Guijarro S, Enjuanes A, Hernández L, Yagüe J, Nicolás P, Romeo-Casabona CM, Himmelbauer H, Castillo E, Dohm JC, de Sanjosé S, Piris MA, de Alava E, San Miguel J, Royo R, Gelpí JL, Torrents D, Orozco M, Pisano DG, Valencia A, Guigó R, Bayés M, Heath S, Gut M, Klatt P, Marshall J, Raine K, Stebbings LA, Futreal PA, Stratton MR, Campbell PJ, Gut I, López-Guillermo A, Estivill X, Montserrat E, López-Otín C, Campo E.

Nature. 2011 Jun 5;475(7354):101-5. doi: 10.1038/nature10113.

20.

MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function.

Miñones-Moyano E, Porta S, Escaramís G, Rabionet R, Iraola S, Kagerbauer B, Espinosa-Parrilla Y, Ferrer I, Estivill X, Martí E.

Hum Mol Genet. 2011 Aug 1;20(15):3067-78. doi: 10.1093/hmg/ddr210. Epub 2011 May 10.

PMID:
21558425
21.

Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis.

Docampo E, Giardina E, Riveira-Muñoz E, de Cid R, Escaramís G, Perricone C, Fernández-Sueiro JL, Maymó J, González-Gay MA, Blanco FJ, Hüffmeier U, Lisbona MP, Martín J, Carracedo A, Reis A, Rabionet R, Novelli G, Estivill X.

Arthritis Rheum. 2011 Jul;63(7):1860-5. doi: 10.1002/art.30340.

22.

Spatio-temporal analysis of mortality among children under the age of five in Manhiça (Mozambique) during the period 1997-2005.

Escaramís G, Carrasco JL, Aponte JJ, Nhalungo D, Nhacolo A, Alonso P, Ascaso C.

Int J Health Geogr. 2011 Feb 18;10:14. doi: 10.1186/1476-072X-10-14.

23.

Evolutionary dynamics of the Ty3/gypsy LTR retrotransposons in the genome of Anopheles gambiae.

Tubio JM, Tojo M, Bassaganyas L, Escaramis G, Sharakhov IV, Sharakhova MV, Tornador C, Unger MF, Naveira H, Costas J, Besansky NJ.

PLoS One. 2011 Jan 24;6(1):e16328. doi: 10.1371/journal.pone.0016328.

24.

Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6.

Riveira-Munoz E, He SM, Escaramís G, Stuart PE, Hüffmeier U, Lee C, Kirby B, Oka A, Giardina E, Liao W, Bergboer J, Kainu K, de Cid R, Munkhbat B, Zeeuwen PL, Armour JA, Poon A, Mabuchi T, Ozawa A, Zawirska A, Burden AD, Barker JN, Capon F, Traupe H, Sun LD, Cui Y, Yin XY, Chen G, Lim HW, Nair RP, Voorhees JJ, Tejasvi T, Pujol R, Munkhtuvshin N, Fischer J, Kere J, Schalkwijk J, Bowcock A, Kwok PY, Novelli G, Inoko H, Ryan AW, Trembath RC, Reis A, Zhang XJ, Elder JT, Estivill X.

J Invest Dermatol. 2011 May;131(5):1105-9. doi: 10.1038/jid.2010.350. Epub 2010 Nov 25.

25.

Variants in estrogen receptor alpha gene are associated with phenotypical expression of obsessive-compulsive disorder.

Alonso P, Gratacòs M, Segalàs C, Escaramís G, Real E, Bayés M, Labad J, Pertusa A, Vallejo J, Estivill X, Menchón JM.

Psychoneuroendocrinology. 2011 May;36(4):473-83. doi: 10.1016/j.psyneuen.2010.07.022. Epub 2010 Sep 17.

PMID:
20850223
26.

Genetic variants and abnormal processing of pre-miR-182, a circadian clock modulator, in major depression patients with late insomnia.

Saus E, Soria V, Escaramís G, Vivarelli F, Crespo JM, Kagerbauer B, Menchón JM, Urretavizcaya M, Gratacòs M, Estivill X.

Hum Mol Genet. 2010 Oct 15;19(20):4017-25. doi: 10.1093/hmg/ddq316. Epub 2010 Jul 23.

PMID:
20656788
27.

A haplotype of glycogen synthase kinase 3β is associated with early onset of unipolar major depression.

Saus E, Soria V, Escaramís G, Crespo JM, Valero J, Gutiérrez-Zotes A, Martorell L, Vilella E, Menchón JM, Estivill X, Gratacòs M, Urretavizcaya M.

Genes Brain Behav. 2010 Oct;9(7):799-807. doi: 10.1111/j.1601-183X.2010.00617.x. Epub 2010 Aug 4.

28.

Response to methadone maintenance treatment is associated with the MYOCD and GRM6 genes.

Fonseca F, Gratacòs M, Escaramís G, De Cid R, Martín-Santos R, Fernández-Espejo E, Estivill X, Torrens M.

Mol Diagn Ther. 2010 Jun 1;14(3):171-8. doi: 10.2165/11537650-000000000-00000.

PMID:
20560679
29.

Resequencing and association analysis of arylalkylamine N-acetyltransferase (AANAT) gene and its contribution to major depression susceptibility.

Soria V, Martínez-Amorós E, Escaramís G, Valero J, Crespo JM, Gutiérrez-Zotes A, Bayés M, Martorell L, Vilella E, Estivill X, Menchón JM, Gratacòs M, Urretavizcaya M.

J Pineal Res. 2010 Aug;49(1):35-44. doi: 10.1111/j.1600-079X.2010.00763.x. Epub 2010 Apr 29.

PMID:
20459461
30.

The total deviation index estimated by tolerance intervals to evaluate the concordance of measurement devices.

Escaramís G, Ascaso C, Carrasco JL.

BMC Med Res Methodol. 2010 Apr 8;10:31. doi: 10.1186/1471-2288-10-31.

31.

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease.

Gratacòs M, Escaramís G, Bustamante M, Saus E, Agüera Z, Bayés M, Cellini E, de Cid R, Fernández-Aranda F, Forcano L, González JR, Gorwood P, Hebebrand J, Hinney A, Mercader JM, Nacmias B, Ramoz N, Ribasés M, Ricca V, Romo L, Sorbi S, Versini A, Estivill X.

J Psychiatr Res. 2010 Oct;44(13):834-40. doi: 10.1016/j.jpsychires.2010.01.009. Epub 2010 Mar 9.

PMID:
20219210
32.

Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis.

Docampo E, Rabionet R, Riveira-Muñoz E, Escaramís G, Julià A, Marsal S, Martín JE, González-Gay MA, Balsa A, Raya E, Martín J, Estivill X.

Arthritis Rheum. 2010 May;62(5):1246-51. doi: 10.1002/art.27381.

33.

Predicting non-sentinel lymph node status in breast cancer patients with sentinel lymph node involvement: evaluation of two scoring systems.

Sanjuán A, Escaramís G, Vidal-Sicart S, Illa M, Zanón G, Pahisa J, Rubí S, Velasco M, Santamaría G, Farrús B, Muñoz M, García Y, Fernández PL, Pons F.

Breast J. 2010 Mar-Apr;16(2):134-40. doi: 10.1111/j.1524-4741.2009.00892.x. Epub 2010 Jan 29.

PMID:
20136644
34.

Association study of 44 candidate genes with depressive and anxiety symptoms in post-partum women.

Costas J, Gratacòs M, Escaramís G, Martín-Santos R, de Diego Y, Baca-García E, Canellas F, Estivill X, Guillamat R, Guitart M, Gutiérrez-Zotes A, García-Esteve L, Mayoral F, Moltó MD, Phillips C, Roca M, Carracedo A, Vilella E, Sanjuán J.

J Psychiatr Res. 2010 Aug;44(11):717-24. doi: 10.1016/j.jpsychires.2009.12.012. Epub 2010 Jan 22.

PMID:
20092830
35.

Differential association of circadian genes with mood disorders: CRY1 and NPAS2 are associated with unipolar major depression and CLOCK and VIP with bipolar disorder.

Soria V, Martínez-Amorós E, Escaramís G, Valero J, Pérez-Egea R, García C, Gutiérrez-Zotes A, Puigdemont D, Bayés M, Crespo JM, Martorell L, Vilella E, Labad A, Vallejo J, Pérez V, Menchón JM, Estivill X, Gratacòs M, Urretavizcaya M.

Neuropsychopharmacology. 2010 May;35(6):1279-89. doi: 10.1038/npp.2009.230. Epub 2010 Jan 13.

36.

Gene expression signatures in breast cancer distinguish phenotype characteristics, histologic subtypes, and tumor invasiveness.

Pedraza V, Gomez-Capilla JA, Escaramis G, Gomez C, Torné P, Rivera JM, Gil A, Araque P, Olea N, Estivill X, Fárez-Vidal ME.

Cancer. 2010 Jan 15;116(2):486-96. doi: 10.1002/cncr.24805.

37.

[Clinical safety and patient oriented care: descriptive study of 113 Spanish hospitals and similarities in other European countries].

Vallejo P, Suñol R, Escaramis G, Torrontegui M, Lombarts K, Bañeres J.

Rev Calid Asist. 2009 Aug;24(4):139-48. doi: 10.1016/S1134-282X(09)71797-X. Spanish.

PMID:
19647675
38.

A brain-derived neurotrophic factor haplotype is associated with therapeutic response in obsessive-compulsive disorder.

Real E, Gratacòs M, Soria V, Escaramís G, Alonso P, Segalàs C, Bayés M, de Cid R, Menchón JM, Estivill X.

Biol Psychiatry. 2009 Oct 1;66(7):674-80. doi: 10.1016/j.biopsych.2009.05.017. Epub 2009 Jul 9.

PMID:
19589503
39.

Accounting for uncertainty when assessing association between copy number and disease: a latent class model.

González JR, Subirana I, Escaramís G, Peraza S, Cáceres A, Estivill X, Armengol L.

BMC Bioinformatics. 2009 Jun 6;10:172. doi: 10.1186/1471-2105-10-172.

40.

Long-term results of biofeedback treatment for faecal incontinence: a comparative study with untreated controls.

Lacima G, Pera M, Amador A, Escaramís G, Piqué JM.

Colorectal Dis. 2010 Aug;12(8):742-9. doi: 10.1111/j.1463-1318.2009.01881.x. Epub 2009 Apr 10.

PMID:
19486084
41.

Implementation of patient safety strategies in European hospitals.

Suñol R, Vallejo P, Groene O, Escaramis G, Thompson A, Kutryba B, Garel P.

Qual Saf Health Care. 2009 Feb;18 Suppl 1:i57-61. doi: 10.1136/qshc.2008.029413.

42.

Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis.

de Cid R, Riveira-Munoz E, Zeeuwen PL, Robarge J, Liao W, Dannhauser EN, Giardina E, Stuart PE, Nair R, Helms C, Escaramís G, Ballana E, Martín-Ezquerra G, den Heijer M, Kamsteeg M, Joosten I, Eichler EE, Lázaro C, Pujol RM, Armengol L, Abecasis G, Elder JT, Novelli G, Armour JA, Kwok PY, Bowcock A, Schalkwijk J, Estivill X.

Nat Genet. 2009 Feb;41(2):211-5. doi: 10.1038/ng.313. Epub 2009 Jan 25.

43.

Recurrence and survival in surgically treated endometrioid endometrial cancer.

Sanjuán A, Cobo T, Escaramís G, Rovirosa A, Ordi J, García S, Hernández S, Caparrós X, Torné A, Martínez Román S, Lejárcegui JA, Pahisa J.

Clin Transl Oncol. 2008 Aug;10(8):505-11.

PMID:
18667382
44.

Genetic susceptibility to obsessive-compulsive hoarding: the contribution of neurotrophic tyrosine kinase receptor type 3 gene.

Alonso P, Gratacòs M, Menchón JM, Segalàs C, González JR, Labad J, Bayés M, Real E, de Cid R, Pertusa A, Escaramís G, Vallejo J, Estivill X.

Genes Brain Behav. 2008 Oct;7(7):778-85. doi: 10.1111/j.1601-183X.2008.00418.x. Epub 2008 Jul 28.

45.

Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds.

Bosch N, Escaramís G, Mercader JM, Armengol L, Estivill X.

Gene. 2008 Sep 1;420(2):113-7. doi: 10.1016/j.gene.2008.05.003. Epub 2008 May 13.

PMID:
18602769
46.

Role of magnetic resonance imaging and cause of pitfalls in detecting myometrial invasion and cervical involvement in endometrial cancer.

Sanjuán A, Escaramís G, Ayuso JR, Román SM, Torné A, Ordi J, Lejárcegui JA, Pahisa J.

Arch Gynecol Obstet. 2008 Dec;278(6):535-9. doi: 10.1007/s00404-008-0636-1. Epub 2008 Mar 27.

PMID:
18368415
47.

Detection of significant disease risks using a spatial conditional autoregressive model.

Escaramís G, Carrasco JL, Ascaso C.

Biometrics. 2008 Dec;64(4):1043-53. doi: 10.1111/j.1541-0420.2007.00981.x. Epub 2008 Feb 7.

PMID:
18261162
48.

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.

Mercader JM, Saus E, Agüera Z, Bayés M, Boni C, Carreras A, Cellini E, de Cid R, Dierssen M, Escaramís G, Fernández-Aranda F, Forcano L, Gallego X, González JR, Gorwood P, Hebebrand J, Hinney A, Nacmias B, Puig A, Ribasés M, Ricca V, Romo L, Sorbi S, Versini A, Gratacòs M, Estivill X.

Hum Mol Genet. 2008 May 1;17(9):1234-44. doi: 10.1093/hmg/ddn013. Epub 2008 Jan 18.

PMID:
18203754
49.

Reduction in the prevalence and intensity of infection in Onchocerca volvulus microfilariae according to ethnicity and community after 8 years of ivermectin treatment on the island of Bioko, Equatorial Guinea.

Mas J, Ascaso C, Escaramis G, Abellana R, Duran E, Sima A, Sánchez MJ, Nkogo PR, Nguema R, Untoria MD, Echeverria MA, Ardevol MM, de Jiménez Anta MT.

Trop Med Int Health. 2006 Jul;11(7):1082-91.

50.

Renal expression of ICAM-1 and VCAM-1 in ANCA-associated glomerulonephritis--are there differences among serologic subgroups?

Arrizabalaga P, Solé M, Iglesias C, Escaramís G, Ascaso C.

Clin Nephrol. 2006 Feb;65(2):79-86.

PMID:
16509455

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