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Association of Urinary Sodium, Potassium, and the Sodium-to-Potassium Ratio with Impaired Kidney Function Assessed with 24-H Urine Analysis.
Zakauskiene U, Bratcikoviene N, Macioniene E, Zabuliene L, Sukackiene D, Linkeviciute-Dumce A, Karosiene D, Banys V, Migline V, Utkus A, Miglinas M
Nutrients, 16(19):3400, 07 Oct 2024
Cited by: 0 articles | PMID: 39408367 | PMCID: PMC11478606
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Utilization of Microfluidic Droplet-Based Methods in Diagnosis and Treatment Methods of Hepatocellular Carcinoma: A Review.
Zajanckauskaite A, Lingelbach M, Juozapaitė D, Utkus A, Rukšnaitytė G, Jonuškienė G, Gulla A
Genes (Basel), 15(10):1242, 25 Sep 2024
Cited by: 0 articles | PMID: 39457366 | PMCID: PMC11508129
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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Epi25 Collaborative
Nat Neurosci, 27(10):1864-1879, 03 Oct 2024
Cited by: 0 articles | PMID: 39363051
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Higher levels of plasma Adrenocorticotropic hormone (ACTH) are associated with lower suicidal ideation in depressed patients compared to controls and suicide attempters, independently from depression severity.
Strumila R, Lengvenyte A, Zdanavicius L, Badaras R, Dlugauskas E, Lesinskiene S, Matiekus E, Marcinkevicius M, Venceviciene L, Utkus A, Kaminskas A, Petrenas T, Songailiene J, Vitkus D, Ambrozaityte L
Compr Psychoneuroendocrinol, 19:100235, 26 Apr 2024
Cited by: 1 article | PMID: 38737407 | PMCID: PMC11087924
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Unraveling the Pathogenetic Mechanisms Underlying the Association between Specific Mitochondrial DNA Haplogroups and Parkinson's Disease.
Lan MY, Lin TK, Lace B, Utkus A, Burnyte B, Grigalioniene K, Lin YH, Inashkina I, Liou CW
Cells, 13(8):694, 17 Apr 2024
Cited by: 0 articles | PMID: 38667309 | PMCID: PMC11049488
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Neuropsychiatric Aspects of Sotos Syndrome: Explorative Review Building Multidisciplinary Bridges in Clinical Practice.
Lesinskiene S, Montvilaite R, Pociute K, Matuleviciene A, Utkus A
J Clin Med, 13(8):2204, 11 Apr 2024
Cited by: 2 articles | PMID: 38673476 | PMCID: PMC11051337
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Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease.
Grigalionienė K, Burnytė B, Ambrozaitytė L, Utkus A
Orphanet J Rare Dis, 18(1):307, 02 Oct 2023
Cited by: 1 article | PMID: 37784170 | PMCID: PMC10544509
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Fetal Alcohol Spectrum Disorders and Inadequacy of Care: Importance of Raising Awareness in Clinical Practice.
Lesinskienė S, Žilinskas E, Utkus A, Marčiukaitytė R, Vasiliauskaitė G, Stankevičiūtė R, Kinčinienė O
Children (Basel), 11(1):5, 20 Dec 2023
Cited by: 1 article | PMID: 38275426 | PMCID: PMC10814035
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Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in Genomics.
Rancelis T, Domarkiene I, Ambrozaityte L, Utkus A
Genes (Basel), 14(8):1630, 16 Aug 2023
Cited by: 1 article | PMID: 37628681 | PMCID: PMC10454355
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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.
International League Against Epilepsy Consortium on Complex Epilepsies
Nat Genet, 55(9):1471-1482, 31 Aug 2023
Cited by: 32 articles | PMID: 37653029 | PMCID: PMC10484785
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Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe - A multi-professional survey study.
Koido K, Malmgren CI, Pojskic L, Almos PZ, Bergen SE, Borg I, Božina N, Coviello DA, Degenhardt F, Ganoci L, Jensen UB, Durand-Lennad L, Laurent-Levinson C, McQuillin A, Navickas A, Pace NP, Paneque M, Rietschel M, Grigoroiu-Serbanescu M, [...] Tammimies K
Eur J Med Genet, 66(8):104805, 03 Jul 2023
Cited by: 3 articles | PMID: 37406854
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Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.
Siavrienė E, Petraitytė G, Mikštienė V, Maldžienė Ž, Sasnauskienė A, Žitkutė V, Ambrozaitytė L, Rančelis T, Utkus A, Kučinskas V, Preikšaitienė E
Medicina (Kaunas), 59(7):1225, 29 Jun 2023
Cited by: 0 articles | PMID: 37512036 | PMCID: PMC10385642
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Association of hair glucocorticoid levels with sleep quality indicators: a pilot study in apparently healthy perimenopausal and menopausal women.
Mazgelytė E, Valatkevičiūtė A, Songailienė J, Utkus A, Burokienė N, Karčiauskaitė D
Front Endocrinol (Lausanne), 14:1186014, 17 Jul 2023
Cited by: 2 articles | PMID: 37529598 | PMCID: PMC10390219
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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Montanucci L, Lewis-Smith D, Collins RL, Niestroj LM, Parthasarathy S, Xian J, Ganesan S, Macnee M, Brünger T, Thomas RH, Talkowski M, Epi25 Collaborative, Helbig I, Leu C, Lal D
Nat Commun, 14(1):4392, 20 Jul 2023
Cited by: 8 articles | PMID: 37474567 | PMCID: PMC10359300
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A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects.
Kalinauskiene R, Brazdziunaite D, Burokiene N, Dirsė V, Morkuniene A, Utkus A, Preiksaitiene E
Medicina (Kaunas), 59(6):1156, 15 Jun 2023
Cited by: 0 articles | PMID: 37374360 | PMCID: PMC10302461
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Cerebellar Ataxia and Peripheral Neuropathy in a Family With PNPLA8-Associated Disease.
Burnyte B, Vilimiene R, Grigalioniene K, Adomaitiene I, Utkus A
Neurol Genet, 9(3):e200068, 10 Apr 2023
Cited by: 2 articles | PMID: 37057294 | PMCID: PMC10088641
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Identification of a novel BICRA variant leading to the newly described Coffin-Siris syndrome 12.
Asadauskaitė G, Morkūnienė A, Utkus A, Burnytė B
Brain Dev, 45(3):185-190, 24 Nov 2022
Cited by: 1 article | PMID: 36437209
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The academic impact and value of an international online surgery lecture series.
Hashimoto D, Gulla A, Satoi S, Yamamoto T, Yamaki S, Matsui Y, Ohe C, Yamasaki M, Hamada M, Ikeura T, Shimatani M, Breugelmans R, Utkus A, Poskus T, Samuilis A, Miglinas M, Laurinavicius A, Tomoda K, Hendrixson V, [...] Strupas K
Surg Today, 53(9):1100-1104, 15 Feb 2023
Cited by: 0 articles | PMID: 36790475 | PMCID: PMC9930694
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Significantly elevated phosphatidylethanol levels in recent suicide attempters, but not in depressed controls and healthy volunteers.
Strumila R, Lengvenyte A, Zdanavicius L, Badaras R, Dlugauskas E, Lesinskiene S, Matiekus E, Marcinkevicius M, Venceviciene L, Utkus A, Kaminskas A, Petrenas T, Songailiene J, Ambrozaityte L
J Psychiatr Res, 158:245-254, 27 Dec 2022
Cited by: 1 article | PMID: 36608540
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Rare disease education in Europe and beyond: time to act.
Tumiene B, Peters H, Melegh B, Peterlin B, Utkus A, Fatkulina N, Pfliegler G, Graessner H, Hermanns S, Scarpa M, Blay JY, Ashton S, McKay L, Baynam G
Orphanet J Rare Dis, 17(1):441, 19 Dec 2022
Cited by: 9 articles | PMID: 36536417 | PMCID: PMC9761619
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Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
Grigalionienė K, Burnytė B, Balkelienė D, Ambrozaitytė L, Utkus A
Mol Genet Genomic Med, 11(1):e2059, 01 Oct 2022
Cited by: 4 articles | PMID: 36181358 | PMCID: PMC9834195
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Dynamics of Physiological, Biochemical and Psychological Markers during Single Session of Virtual Reality-Based Respiratory Biofeedback Relaxation.
Mazgelytė E, Zagorskaja J, Dereškevičiūtė E, Petrėnas T, Kaminskas A, Songailienė J, Utkus A, Chomentauskas G, Karčiauskaitė D
Behav Sci (Basel), 12(12):482, 28 Nov 2022
Cited by: 1 article | PMID: 36546965 | PMCID: PMC9774569
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Challenges in the Diagnosis of XY Differences of Sexual Development.
Bumbulienė Ž, Bužinskienė D, Banuškevičienė G, Šidlovska E, Preikšaitienė E, Utkus A
Medicina (Kaunas), 58(12):1736, 27 Nov 2022
Cited by: 1 article | PMID: 36556938 | PMCID: PMC9787768
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HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.
Malcorps M, Amor-Barris S, Burnyte B, Vilimiene R, Armirola-Ricaurte C, Grigalioniene K, Ekshteyn A, Morkuniene A, Vaitkevicius A, De Vriendt E, Baets J, Scherer SS, Ambrozaityte L, Utkus A, Jordanova A, Peeters K
Orphanet J Rare Dis, 17(1):374, 14 Oct 2022
Cited by: 1 article | PMID: 36242072 | PMCID: PMC9569031
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PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.
Siavrienė E, Maldžienė Ž, Mikštienė V, Petraitytė G, Rančelis T, Dapkūnas J, Burnytė B, Benušienė E, Sasnauskienė A, Grikinienė J, Griškevičiūtė E, Utkus A, Preikšaitienė E
Medicina (Kaunas), 58(11):1526, 26 Oct 2022
Cited by: 3 articles | PMID: 36363484 | PMCID: PMC9693321
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1-25 of 121 results

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Search life-sciences literature (45,104,145 articles, preprints and more)

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Association of Urinary Sodium, Potassium, and the Sodium-to-Potassium Ratio with Impaired Kidney Function Assessed with 24-H Urine Analysis.

Utilization of Microfluidic Droplet-Based Methods in Diagnosis and Treatment Methods of Hepatocellular Carcinoma: A Review.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Higher levels of plasma Adrenocorticotropic hormone (ACTH) are associated with lower suicidal ideation in depressed patients compared to controls and suicide attempters, independently from depression severity.

Unraveling the Pathogenetic Mechanisms Underlying the Association between Specific Mitochondrial DNA Haplogroups and Parkinson's Disease.

Neuropsychiatric Aspects of Sotos Syndrome: Explorative Review Building Multidisciplinary Bridges in Clinical Practice.

Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease.

Fetal Alcohol Spectrum Disorders and Inadequacy of Care: Importance of Raising Awareness in Clinical Practice.

Implementing Core Genes and an Omnigenic Model for Behaviour Traits Prediction in Genomics.

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.

Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe - A multi-professional survey study.

Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.

Association of hair glucocorticoid levels with sleep quality indicators: a pilot study in apparently healthy perimenopausal and menopausal women.

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

A De Novo 8q22.2q22.3 Interstitial Microdeletion in a Girl with Developmental Delay and Congenital Defects.

Cerebellar Ataxia and Peripheral Neuropathy in a Family With PNPLA8-Associated Disease.

Identification of a novel BICRA variant leading to the newly described Coffin-Siris syndrome 12.

The academic impact and value of an international online surgery lecture series.

Significantly elevated phosphatidylethanol levels in recent suicide attempters, but not in depressed controls and healthy volunteers.

Rare disease education in Europe and beyond: time to act.

Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.

Dynamics of Physiological, Biochemical and Psychological Markers during Single Session of Virtual Reality-Based Respiratory Biofeedback Relaxation.

Challenges in the Diagnosis of XY Differences of Sexual Development.

HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.

PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.

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