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

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Genome-wide association study of borderline personality disorder identifies six loci and highlights shared risk with mental and somatic disorders
Streit F, Awasthi S, Hall AS, Niarchou M, Marouli E, Babajide O, Braun A, Frank J, Zillich L, Callies C, Avetyan D, Zillich E, Naamanka J, Aherrahrou Z, Ahmad Z, Ask H, Batzler A, Benros ME, Brand-de Wilde OM, [...] Witt SH
medRxiv, 13 Nov 2024
Cited by: 0 articles | PPR: PPR939284
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Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction.
Braun A, Shekhar S, Levey DF, Straub P, Kraft J, Panagiotaropoulou GM, Heilbron K, Awasthi S, Meleka Hanna R, Hoffmann S, Stein M, Lehnerer S, Mergenthaler P, Elnahas AG, Topaloudi A, Koromina M, Palviainen T, Asbjornsdottir B, Stefansson H, [...] Ripke S
Nat Commun, 15(1):9839, 13 Nov 2024
Cited by: 0 articles | PMID: 39537604 | PMCID: PMC11560923
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Cross-EHR validation of antidepressant response algorithm and links with genetics of psychiatric traits
Sealock JM, Tubbs JD, Lake AM, Straub P, Smoller JW, Davis LK
medRxiv, 12 Sep 2024
Cited by: 0 articles | PPR: PPR909628
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Descriptive epidemiology of 399 histologically confirmed newly diagnosed meningeal solitary fibrous tumours and haemangiopericytomas in France: 2006-2015.
Champeaux Depond C, Zouaoui S, Darlix A, Rigau V, Mathieu-Daudé H, Bauchet F, Khettab M, Trétarre B, Figarella-Branger D, Taillandier L, Boetto J, Pallud J, Peyre M, Lottin M, Bauchet L, French Brain Tumour DataBase (FBTDB) Participants and Investigators with the participation of the Société française de neurochirurgie (SFNC), Club de neuro-oncologie de la société française de neurochirurgie, Société française de neuropathologie (SFNP), Association des neuro-oncologues d’expression française (ANOCEF)
Acta Neurochir (Wien), 166(1):320, 02 Aug 2024
Cited by: 0 articles | PMID: 39093339
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Descriptive epidemiology of 30,223 histopathologically confirmed meningiomas in France: 2006-2015.
Depond CC, Zouaoui S, Darlix A, Rigau V, Mathieu-Daudé H, Bauchet F, Khettab M, Trétarre B, Figarella-Branger D, Taillandier L, Boetto J, Pallud J, Zemmoura I, Roche PH, Bauchet L, French Brain Tumour DataBase (FBTDB) Participants, Investigators with the participation of the Société française de neurochirurgie (SFNC), Club de neuro-oncologie de la société française de neurochirurgie, Société française de neuropathologie (SFNP), Association des neuro-oncologues d’expression française (ANOCEF)
Acta Neurochir (Wien), 166(1):214, 14 May 2024
Cited by: 1 article | PMID: 38740641
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Sex differences in immune function and disease risk are not easily explained by an evolutionary mismatch
Arner AM, Muhoya B, Rozado MS, Gurven MR, Kahumbu J, Kamau J, Kinyua P, Lotukoi F, Martins DJ, Miano C, Montague MJ, Njeru S, Peng J, Straub P, Watowich MM, Davis LK, Snyder-Mackler N, Ayroles JF, Lea AJ
bioRxiv, 16 Feb 2024
Cited by: 0 articles | PPR: PPR819622
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Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation.
Lo Faro V, Bhattacharya A, Zhou W, Zhou D, Wang Y, Läll K, Kanai M, Lopera-Maya E, Straub P, Pawar P, Tao R, Zhong X, Namba S, Global Biobank Meta-analysis Initiative, Sanna S, Nolte IM, Okada Y, Ingold N, MacGregor S, [...] Hirbo J
Cell Rep Med, 5(2):101430, 01 Feb 2024
Cited by: 7 articles | PMID: 38382466 | PMCID: PMC10897632
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Fine-scale sampling uncovers the complexity of migrations in 5th-6th century Pannonia.
Vyas DN, Koncz I, Modi A, Mende BG, Tian Y, Francalacci P, Lari M, Vai S, Straub P, Gallina Z, Szeniczey T, Hajdu T, Pejrani Baricco L, Giostra C, Radzevičiūtė R, Hofmanová Z, Évinger S, Bernert Z, Pohl W, [...] Veeramah KR
Curr Biol, 33(18):3951-3961.e11, 25 Aug 2023
Cited by: 1 article | PMID: 37633281
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Exploring genetic risk for catatonia in a genome wide association study and polygenic risk score analysis.
Wilson JE, Sealock J, Straub P, Raman R, Kipp AM, Dittus RS, Heckers S, Ely W, Davis LK
Schizophr Res, 263:178-190, 28 Jul 2023
Cited by: 1 article | PMID: 37517919
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Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.
Hirbo JB, Pasutto F, Gamazon ER, Evans P, Pawar P, Berner D, Sealock J, Tao R, Straub PS, Konkashbaev AI, Breyer MA, Schlötzer-Schrehardt U, Reis A, Brantley MA, Khor CC, Joos KM, Cox NJ
BMC Genomics, 24(1):75, 16 Feb 2023
Cited by: 2 articles | PMID: 36797672 | PMCID: PMC9936777
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Association Between Genetically Predicted Expression of TPMT and Azathioprine Adverse Events
Davis A, Dickson AL, Daniel LL, Nepal P, Zanussi J, Miller-Fleming TW, Straub PS, Wei W, Liu G, Cox NJ, Hung AM, Feng Q, Stein CM, Chung CP
Research Square, 13 Jan 2023
Cited by: 0 articles | PPR: PPR596789
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Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts.
Wang Y, Namba S, Lopera E, Kerminen S, Tsuo K, Läll K, Kanai M, Zhou W, Wu KH, Favé MJ, Bhatta L, Awadalla P, Brumpton B, Deelen P, Hveem K, Lo Faro V, Mägi R, Murakami Y, Sanna S, [...] Hirbo J
Cell Genom, 3(1):100241, 04 Jan 2023
Cited by: 46 articles | PMID: 36777179 | PMCID: PMC9903818
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Genes associated with depression and coronary artery disease are enriched for inflammation and cardiomyopathy-associated pathways
Singh K, Lee H, Sealock JM, Miller-Flemming T, Straub P, Cox NJ, Wells QS, Smoller JW, Hodges EC, Davis LK
medRxiv, 26 Oct 2022
Cited by: 0 articles | PPR: PPR562070
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Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease.
Zhou W, Kanai M, Wu KH, Rasheed H, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Lo Faro V, Lopera-Maya EA, Läll K, Favé MJ, Partanen JJ, Chapman SB, Karjalainen J, [...] Neale BM
Cell Genom, 2(10):100192, 12 Oct 2022
Cited by: 140 articles | PMID: 36777996 | PMCID: PMC9903716
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Fine-scale sampling uncovers the complexity of migrations in 5th-6th century Pannonia
Vyas DN, Koncz I, Modi A, Mende BG, Tian Y, Francalacci P, Lari M, Vai S, Straub P, Gallina Z, Szeniczey T, Hajdu T, Radzevičiūtė R, Hofmanová Z, Évinger S, Bernert Z, Pohl W, Caramelli D, Vida T, [...] Veeramah KR
bioRxiv, 27 Sep 2022
Cited by: 0 articles | PPR: PPR550774
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Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth.
Abraham A, Le B, Kosti I, Straub P, Velez-Edwards DR, Davis LK, Newton JM, Muglia LJ, Rokas A, Bejan CA, Sirota M, Capra JA
BMC Med, 20(1):333, 28 Sep 2022
Cited by: 11 articles | PMID: 36167547 | PMCID: PMC9516830
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A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.
Niarchou M, Sealock JM, Straub P, Sanchez-Roige S, Sutcliffe JS, Davis LK
Am J Med Genet B Neuropsychiatr Genet, 189(6):185-195, 15 Jul 2022
Cited by: 2 articles | PMID: 35841203 | PMCID: PMC9378640
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Investigating the genetic pathways of insomnia in Autism Spectrum Disorder.
Niarchou M, Singer EV, Straub P, Malow BA, Davis LK
Res Dev Disabil, 128:104299, 09 Jul 2022
Cited by: 0 articles | PMID: 35820265 | PMCID: PMC10068748
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Identifying High-Risk Comorbidities Associated with Opioid Use Patterns Using Electronic Health Record Prescription Data.
Jennings MV, Lee H, Rocha DB, Bianchi SB, Coombes BJ, Crist RC, Faucon AB, Hu Y, Kember RL, Mallard TT, Niarchou M, Poulsen MN, Straub P, Urman RD, Walsh CG, Davis LK, Smoller JW, Troiani V, Sanchez-Roige S
Complex Psychiatry, 8(1-2):47-55, 02 Jun 2022
Cited by: 7 articles | PMID: 36545045 | PMCID: PMC9669950
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Genome-wide association study of musical beat synchronization demonstrates high polygenicity.
Niarchou M, Gustavson DE, Sathirapongsasuti JF, Anglada-Tort M, Eising E, Bell E, McArthur E, Straub P, 23andMe Research Team, McAuley JD, Capra JA, Ullén F, Creanza N, Mosing MA, Hinds DA, Davis LK, Jacoby N, Gordon RL
Nat Hum Behav, 6(9):1292-1309, 16 Jun 2022
Cited by: 33 articles | PMID: 35710621 | PMCID: PMC9489530
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Investigating the genetic pathways of insomnia in Autism Spectrum Disorder
Niarchou M, Singer EV, Straub P, Malow BA, Davis LK
medRxiv, 04 Feb 2022
Cited by: 0 articles | PPR: PPR450228
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Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity.
Daniel LL, Dickson AL, Zanussi JT, Miller-Fleming TW, Straub PS, Wei WQ, Plummer WD, Dupont WD, Liu G, Anandi P, Reese TS, Birdwell KA, Kawai VK, Hung AM, Cox NJ, Feng Q, Stein CM, Chung CP
Clin Transl Sci, 15(4):859-865, 20 Feb 2022
Cited by: 2 articles | PMID: 35118815 | PMCID: PMC9010278
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Genome-wide association meta-analysis identifies novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation
Faro VL, Bhattacharya A, Zhou W, Zhou D, Wang Y, Läll K, Kanai M, Lopera-Maya E, Straub P, Pawar P, Tao R, Zhong X, Namba S, the Global Biobank Meta-analysis Initiative, Sanna S, Nolte IM, Okada Y, Ingold N, MacGregor S, [...] Hirbo J
medRxiv, 17 Dec 2021
Cited by: 0 articles | PPR: PPR433554
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Global Biobank Meta-analysis Initiative: powering genetic discovery across human diseases
Zhou W, Kanai M, Wu KH, Humaira R, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Faro VL, Lopera-Maya EA, Läll K, Favé M, Chapman SB, Karjalainen J, Kurki M, [...] Neale BM
medRxiv, 21 Nov 2021
Cited by: 0 articles | PPR: PPR423598
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Use of the PsycheMERGE Network to Investigate the Association Between Depression Polygenic Scores and White Blood Cell Count.
Sealock JM, Lee YH, Moscati A, Venkatesh S, Voloudakis G, Straub P, Singh K, Feng YA, Ge T, Roussos P, Smoller JW, Chen G, Davis LK
JAMA Psychiatry, 78(12):1365-1374, 01 Dec 2021
Cited by: 19 articles | PMID: 34668925 | PMCID: PMC8529528
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