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Items: 1 to 50 of 512

1.

MiRNA as biomarker for uveitis - A systematic review of the literature.

Pockar S, Petrovic MG, Peterlin B, Valentincic NV.

Gene. 2019 Feb 11. pii: S0378-1119(19)30104-0. doi: 10.1016/j.gene.2019.02.004. [Epub ahead of print] Review.

PMID:
30763668
2.

Migraine Age of Onset and Association With Ischemic Stroke in Late Life: 20 Years Follow-Up in ARIC.

Androulakis XM, Sen S, Kodumuri N, Zhang T, Grego J, Rosamond W, Gottesman RF, Shahar E, Peterlin BL.

Headache. 2019 Jan 21. doi: 10.1111/head.13468. [Epub ahead of print]

PMID:
30663778
3.

Rare missense TUBGCP5 gene variant in a patient with primary microcephaly.

Maver A, Čuturilo G, Kovanda A, Miletić A, Peterlin B.

Eur J Med Genet. 2018 Dec 10. pii: S1769-7212(18)30274-X. doi: 10.1016/j.ejmg.2018.12.003. [Epub ahead of print]

PMID:
30543990
4.

Author response: Body composition status and the risk of migraine: A meta-analysis.

Gelaye B, Sacco S, Brown W, Nitchie H, Ornello R, Peterlin BL.

Neurology. 2018 Dec 4;91(23):1074. doi: 10.1212/WNL.0000000000006627. No abstract available.

PMID:
30510026
5.

Procyanidin trimer C1 reactivates latent HIV as a triple combination therapy with kansui and JQ1.

Cary DC, Peterlin BM.

PLoS One. 2018 Nov 26;13(11):e0208055. doi: 10.1371/journal.pone.0208055. eCollection 2018.

6.

Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.

Loges NT, Antony D, Maver A, Deardorff MA, Güleç EY, Gezdirici A, Nöthe-Menchen T, Höben IM, Jelten L, Frank D, Werner C, Tebbe J, Wu K, Goldmuntz E, Čuturilo G, Krock B, Ritter A, Hjeij R, Bakey Z, Pennekamp P, Dworniczak B, Brunner H, Peterlin B, Tanidir C, Olbrich H, Omran H, Schmidts M.

Am J Hum Genet. 2018 Dec 6;103(6):995-1008. doi: 10.1016/j.ajhg.2018.10.020. Epub 2018 Nov 21.

7.

Family History as an Important Factor for Stratifying Participants in Genetic Studies of Major Depression.

Zalar B, Blatnik A, Maver A, Klemenc-Ketiš Z, Peterlin B.

Balkan J Med Genet. 2018 Oct 29;21(1):5-12. doi: 10.2478/bjmg-2018-0010. eCollection 2018 Jun.

8.

HEXIM1-Tat chimera inhibits HIV-1 replication.

Leoz M, Kukanja P, Luo Z, Huang F, Cary DC, Peterlin BM, Fujinaga K.

PLoS Pathog. 2018 Nov 5;14(11):e1007402. doi: 10.1371/journal.ppat.1007402. eCollection 2018 Nov.

9.

Association between angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to preterm birth: A case-control study and meta-analysis.

Hočevar K, Peterlin A, Jovanović AM, Božović A, Ristanović M, Tul N, Peterlin B.

Eur J Obstet Gynecol Reprod Biol. 2018 Dec;231:122-128. doi: 10.1016/j.ejogrb.2018.09.019. Epub 2018 Sep 11.

PMID:
30366344
10.

DNA Methylation Profiles in Whole Blood of Huntington's Disease Patients.

Zadel M, Maver A, Kovanda A, Peterlin B.

Front Neurol. 2018 Aug 14;9:655. doi: 10.3389/fneur.2018.00655. eCollection 2018.

11.

Contemporary scope of inborn errors of metabolism involving epilepsy or seizures.

Tumienė B, Peterlin B, Maver A, Utkus A.

Metab Brain Dis. 2018 Jul 13. doi: 10.1007/s11011-018-0288-1. [Epub ahead of print] Review.

PMID:
30006695
12.

Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability.

Lovrecic L, Gnan C, Baldan F, Franzoni A, Bertok S, Damante G, Isidor B, Peterlin B.

Mol Cytogenet. 2018 Jun 20;11:39. doi: 10.1186/s13039-018-0388-y. eCollection 2018.

13.

Clinical exome sequencing in dementias: a preliminary study.

Zalar B, Maver A, Kovanda A, Peterlin A, Peterlin B.

Psychiatr Danub. 2018 Jun;30(2):216-219. doi: 10.24869/psyd.2018.216.

14.

The Role of Microbiota in Depression - a brief review.

Zalar B, Haslberger A, Peterlin B.

Psychiatr Danub. 2018 Jun;30(2):136-141. doi: 10.24869/psyd.2018.136. Review.

15.

Polymorphism of the ADRB2 Rs1042713 Gene is not Associated with Spontaneous Preterm Birth: Analyses in a Slovenian Sample and Meta Analysis.

A P, A M, Z J, L L, N T, B P.

Balkan J Med Genet. 2017 Dec 29;20(2):35-42. doi: 10.1515/bjmg-2017-0032. eCollection 2017 Dec.

16.

Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion.

Hodžić A, Lavtar P, Ristanović M, Novaković I, Dotlić J, Peterlin B.

PLoS One. 2018 May 16;13(5):e0196345. doi: 10.1371/journal.pone.0196345. eCollection 2018.

17.

Genetic variations in circadian rhythm genes and susceptibility for myocardial infarction.

Škrlec I, Milic J, Heffer M, Peterlin B, Wagner J.

Genet Mol Biol. 2018 Apr./Jun;41(2):403-409. doi: 10.1590/1678-4685-GMB-2017-0147. Epub 2018 May 14.

18.

Sarcoidosis Related Novel Candidate Genes Identified by Multi-Omics Integrative Analyses.

Hočevar K, Maver A, Kunej T, Peterlin B.

OMICS. 2018 May;22(5):322-331. doi: 10.1089/omi.2018.0027. Epub 2018 Apr 24.

PMID:
29688803
19.

Transcriptomic Biomarkers for Huntington's Disease: Are Gene Expression Signatures in Whole Blood Reliable Biomarkers?

Zadel M, Maver A, Kovanda A, Peterlin B.

OMICS. 2018 Apr;22(4):283-294. doi: 10.1089/omi.2017.0206.

PMID:
29652574
20.

Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping.

Lovrečić L, Rajar P, Volk M, Bertok S, Gnidovec Stražišar B, Osredkar D, Jekovec Vrhovšek M, Peterlin B.

J Appl Genet. 2018 May;59(2):179-185. doi: 10.1007/s13353-018-0440-y. Epub 2018 Mar 21.

PMID:
29564645
21.

Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample.

Ishorst N, Francheschelli P, Böhmer AC, Khan MFJ, Heilmann-Heimbach S, Fricker N, Little J, Steegers-Theunissen RPM, Peterlin B, Nowak S, Martini M, Kruse T, Dunsche A, Kreusch T, Gölz L, Aldhorae K, Halboub E, Reutter H, Mossey P, Nöthen MM, Rubini M, Ludwig KU, Knapp M, Mangold E.

Birth Defects Res. 2018 Jun 1;110(10):871-882. doi: 10.1002/bdr2.1213. Epub 2018 Mar 2.

PMID:
29498243
22.

Mutations in SCN3A cause early infantile epileptic encephalopathy.

Zaman T, Helbig I, Božović IB, DeBrosse SD, Bergqvist AC, Wallis K, Medne L, Maver A, Peterlin B, Helbig KL, Zhang X, Goldberg EM.

Ann Neurol. 2018 Apr;83(4):703-717. doi: 10.1002/ana.25188. Epub 2018 Mar 30.

PMID:
29466837
23.

Bromodomain-containing protein 4-independent transcriptional activation by autoimmune regulator (AIRE) and NF-κB.

Huang F, Shao W, Fujinaga K, Peterlin BM.

J Biol Chem. 2018 Apr 6;293(14):4993-5004. doi: 10.1074/jbc.RA117.001518. Epub 2018 Feb 20.

PMID:
29463681
24.

Screening for Rare Genetic Variants Associated with Atherosclerosis: Opportunity for Personalized Medicine.

Peterlin A, Petrovič D, Peterlin B.

Curr Vasc Pharmacol. 2019;17(1):25-28. doi: 10.2174/1570161116666180206111725.

PMID:
29412113
25.

Viral protein Nef is detected in plasma of half of HIV-infected adults with undetectable plasma HIV RNA.

Ferdin J, Goričar K, Dolžan V, Plemenitaš A, Martin JN, Peterlin BM, Deeks SG, Lenassi M.

PLoS One. 2018 Jan 24;13(1):e0191613. doi: 10.1371/journal.pone.0191613. eCollection 2018.

26.

Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.

Lavtar P, Rudolf G, Maver A, Hodžić A, Starčević Čizmarević N, Živković M, Šega Jazbec S, Klemenc Ketiš Z, Kapović M, Dinčić E, Raičević R, Sepčić J, Lovrečić L, Stanković A, Ristić S, Peterlin B.

PLoS One. 2018 Jan 11;13(1):e0190601. doi: 10.1371/journal.pone.0190601. eCollection 2018.

27.

Fab-based inhibitors reveal ubiquitin independent functions for HIV Vif neutralization of APOBEC3 restriction factors.

Binning JM, Smith AM, Hultquist JF, Craik CS, Caretta Cartozo N, Campbell MG, Burton L, La Greca F, McGregor MJ, Ta HM, Bartholomeeusen K, Peterlin BM, Krogan NJ, Sevillano N, Cheng Y, Gross JD.

PLoS Pathog. 2018 Jan 5;14(1):e1006830. doi: 10.1371/journal.ppat.1006830. eCollection 2018 Jan.

28.

Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.

Likar T, Hasanhodžić M, Teran N, Maver A, Peterlin B, Writzl K.

PLoS One. 2018 Jan 2;13(1):e0188578. doi: 10.1371/journal.pone.0188578. eCollection 2018.

29.

Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice.

Tumienė B, Maver A, Writzl K, Hodžić A, Čuturilo G, Kuzmanić-Šamija R, Čulić V, Peterlin B.

Clin Genet. 2018 May;93(5):1057-1062. doi: 10.1111/cge.13203. Epub 2018 Mar 23.

PMID:
29286531
30.

Modulation of salience network intranetwork resting state functional connectivity in women with chronic migraine.

Androulakis XM, Rorden C, Peterlin BL, Krebs K.

Cephalalgia. 2018 Oct;38(11):1731-1741. doi: 10.1177/0333102417748570. Epub 2017 Dec 13.

PMID:
29237282
31.

Natural Products and HIV/AIDS.

Cary DC, Peterlin BM.

AIDS Res Hum Retroviruses. 2018 Jan;34(1):31-38. doi: 10.1089/AID.2017.0232. Epub 2018 Jan 10.

32.

Association Between Migraine and Suicidal Behaviors: A Nationwide Study in the USA.

Friedman LE, Zhong QY, Gelaye B, Williams MA, Peterlin BL.

Headache. 2018 Mar;58(3):371-380. doi: 10.1111/head.13235. Epub 2017 Nov 29.

PMID:
29193052
33.

De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.

Writzl K, Maver A, Kovačič L, Martinez-Valero P, Contreras L, Satrustegui J, Castori M, Faivre L, Lapunzina P, van Kuilenburg ABP, Radović S, Thauvin-Robinet C, Peterlin B, Del Arco A, Hennekam RC.

Am J Hum Genet. 2017 Nov 2;101(5):844-855. doi: 10.1016/j.ajhg.2017.09.017.

34.

Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21.

Volk M, Maver A, Hodžić A, Lovrečić L, Peterlin B.

OMICS. 2017 Oct;21(10):565-570. doi: 10.1089/omi.2017.0123.

35.

Responsible implementation of expanded carrier screening.

Henneman L, Borry P, Chokoshvili D, Cornel MC, van El CG, Forzano F, Hall A, Howard HC, Janssens S, Kayserili H, Lakeman P, Lucassen A, Metcalfe SA, Vidmar L, de Wert G, Dondorp WJ, Peterlin B.

Eur J Hum Genet. 2017 Nov;25(11):1291. doi: 10.1038/ejhg.2017.159.

36.

The challenges of the expanded availability of genomic information: an agenda-setting paper.

Borry P, Bentzen HB, Budin-Ljøsne I, Cornel MC, Howard HC, Feeney O, Jackson L, Mascalzoni D, Mendes Á, Peterlin B, Riso B, Shabani M, Skirton H, Sterckx S, Vears D, Wjst M, Felzmann H.

J Community Genet. 2018 Apr;9(2):103-116. doi: 10.1007/s12687-017-0331-7. Epub 2017 Sep 26.

37.

A Single Nucleotide Polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion.

Barišić A, Pereza N, Hodžić A, Ostojić S, Peterlin B.

Am J Reprod Immunol. 2017 Dec;78(6). doi: 10.1111/aji.12765. Epub 2017 Sep 20.

PMID:
28940947
38.

Analysis of blood-based gene expression in idiopathic Parkinson disease.

Shamir R, Klein C, Amar D, Vollstedt EJ, Bonin M, Usenovic M, Wong YC, Maver A, Poths S, Safer H, Corvol JC, Lesage S, Lavi O, Deuschl G, Kuhlenbaeumer G, Pawlack H, Ulitsky I, Kasten M, Riess O, Brice A, Peterlin B, Krainc D.

Neurology. 2017 Oct 17;89(16):1676-1683. doi: 10.1212/WNL.0000000000004516. Epub 2017 Sep 15.

39.

Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases.

Bergant G, Maver A, Lovrecic L, Čuturilo G, Hodzic A, Peterlin B.

Genet Med. 2018 Mar;20(3):303-312. doi: 10.1038/gim.2017.142. Epub 2017 Sep 14.

PMID:
28914264
40.

Nef is secreted in exosomes from Nef.GFP-expressing and HIV-1-infected human astrocytes.

Pužar Dominkuš P, Ferdin J, Plemenitaš A, Peterlin BM, Lenassi M.

J Neurovirol. 2017 Oct;23(5):713-724. doi: 10.1007/s13365-017-0552-x. Epub 2017 Jul 31.

41.

Migraine and the risk of post-traumatic stress disorder among a cohort of pregnant women.

Friedman LE, Aponte C, Perez Hernandez R, Velez JC, Gelaye B, Sánchez SE, Williams MA, Peterlin BL.

J Headache Pain. 2017 Dec;18(1):67. doi: 10.1186/s10194-017-0775-5. Epub 2017 Jul 6.

42.

Impact of prenatal screening on the prevalence of Down syndrome in Slovenia.

Rudolf G, Tul N, Verdenik I, Volk M, Brezigar A, Kokalj Vokač N, Jeršin N, Prosenc B, Premru Sršen T, Peterlin B.

PLoS One. 2017 Jun 30;12(6):e0180348. doi: 10.1371/journal.pone.0180348. eCollection 2017.

43.

Cataract and optic disk drusen in a patient with glycogenosis and di George syndrome: clinical and molecular report.

Allegrini D, Penco S, Pece A, Autelitano A, Montesano G, Paci S, Montanari C, Maver A, Peterlin B, Damante G, Rossetti L.

BMC Ophthalmol. 2017 Jun 28;17(1):107. doi: 10.1186/s12886-017-0499-y.

44.

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.

Maver A, Lavtar P, Ristić S, Stopinšek S, Simčič S, Hočevar K, Sepčić J, Drulović J, Pekmezović T, Novaković I, Alenka H, Rudolf G, Šega S, Starčević-Čizmarević N, Palandačić A, Zamolo G, Kapović M, Likar T, Peterlin B.

Sci Rep. 2017 Jun 16;7(1):3715. doi: 10.1038/s41598-017-03536-9.

45.

Modulation of intrinsic resting-state fMRI networks in women with chronic migraine.

Androulakis XM, Krebs K, Peterlin BL, Zhang T, Maleki N, Sen S, Rorden C, Herath P.

Neurology. 2017 Jul 11;89(2):163-169. doi: 10.1212/WNL.0000000000004089. Epub 2017 Jun 14.

46.

Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-β treatment response in multiple sclerosis patients: a preliminary report.

Ristić S, Starčević Čizmarević N, Lavtar P, Lovrečić L, Perković O, Sepčić J, Šega Jazbec S, Kapović M, Peterlin B.

Pharmacogenet Genomics. 2017 Jun;27(6):232-235. doi: 10.1097/FPC.0000000000000283.

PMID:
28430710
47.

Body composition status and the risk of migraine: A meta-analysis.

Gelaye B, Sacco S, Brown WJ, Nitchie HL, Ornello R, Peterlin BL.

Neurology. 2017 May 9;88(19):1795-1804. doi: 10.1212/WNL.0000000000003919. Epub 2017 Apr 12.

48.

Hili Inhibits HIV Replication in Activated T Cells.

Peterlin BM, Liu P, Wang X, Cary D, Shao W, Leoz M, Hong T, Pan T, Fujinaga K.

J Virol. 2017 May 12;91(11). pii: e00237-17. doi: 10.1128/JVI.00237-17. Print 2017 Jun 1.

49.

The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis.

Nadalin S, Buretić-Tomljanović A, Lavtar P, Starčević Čizmarević N, Hodžić A, Sepčić J, Kapović M, Peterlin B, Ristić S.

Brain Behav. 2016 Nov 14;7(1):e00600. doi: 10.1002/brb3.600. eCollection 2017 Jan.

50.

Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion.

Müller A, Wagner J, Hodžić A, Maver A, Škrlec I, Heffer M, Zibar L, Peterlin B.

Croat Med J. 2016 Dec 31;57(6):566-571.

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