Akter, H., Rahaman, M. A., Eshaque, T. B., Mohamed, N., Islam, A., Morshed, M., Shahin, Z., Muhaimin, A., Foyzullah, A. M., Mim, R. A., Omar, F. B., Hasan, M. N., Satsangi, D., Ahmed, N., Al Saba, A., Jahan, N., Hossen, M. A., Mondol, M. A., Sakib, A. S. ... Uddin, M. (2025).
Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort.
Genetics in Medicine,
27(1), Article 101282.
https://doi.org/10.1016/j.gim.2024.101282
Borbye-Lorenzen, N., Holmgaard, S., Ottosson, F., Nudel, R., Appadurai, V.
, Laursen, T. M., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Nordentoft, M.
, Børglum, A. D., Mortensen, P. B., Werge, T.
, Benros, M. E., Hougaard, D. M.
& Skogstrand, K. (2025).
High level of immunoglobulin G targeting mycoplasma or cytomegalovirus in the newborn increases risk of ADHD.
Brain, Behavior, and Immunity,
123, 99-107.
https://doi.org/10.1016/j.bbi.2024.09.009
Voloudakis, G., Therrien, K., Tomasi, S., Rajagopal, V. M., Choi, S. W.
, Demontis, D., Fullard, J. F.
, Børglum, A. D., O’Reilly, P. F., Hoffman, G. E. & Roussos, P. (2025).
Neuropsychiatric polygenic scores are weak predictors of professional categories.
Nature Human Behaviour,
9(3), 595-608. Article 2457.
https://doi.org/10.1038/s41562-024-02074-5
Kaas, M., Chofflet, N.
, Bicer, D., Skeldal, S., Duan, J., Feller, B.
, Vilstrup, J., Groth, R., Sivagurunathan, S., Dashti, H.
, Pedersen, J. S., Werge, T.
, Børglum, A. D., Cimini, B. A., Jones, T. R., Claussnitzer, M.
, Madsen, P., Takahashi, H.
, Demontis, D. ... Glerup, S. (2025).
Rare missense variants of the leukocyte common antigen related receptor (LAR) display reduced activity in transcellular adhesion and synapse formation. bioRxiv.
https://doi.org/10.1101/2025.02.16.638491
Montalbano, S., Krebs, M. D., Rosengren, A., Vaez, M., Hellberg, K. L. G.
, Mortensen, P. B., Børglum, A. D., Geschwind, D. H., Raznahan, A., Thompson, W. K., Helenius, D., Werge, T., Ingason, A. & iPSYCH Investigators (2024).
Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology.
npj Genomic Medicine,
9(1), Article 67.
https://doi.org/10.1038/s41525-024-00450-8
Bergstedt, J., Pasman, J. A., Ma, Z., Harder, A., Yao, S., Parker, N., Treur, J. L., Smit, D. J. A., Frei, O., Shadrin, A. A., Meijsen, J. J., Shen, Q., Hägg, S., Tornvall, P., Buil, A., Werge, T., Hjerling-Leffler, J.
, Als, T. D., Børglum, A. D. ... Fang, F. (2024).
Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease.
Nature Cardiovascular Research,
3(6), 754-769.
https://doi.org/10.1038/s44161-024-00488-y
Vaez, M., Montalbano, S., Waples, R., Krebs, M. D., Hellberg, K.-L. G., Gådin, J., Bybjerg-Grauholm, J.
, Mortensen, P. B., Børglum, A. D., Nordentoft, M., Geschwind, D. H., Helenius, D., Werge, T., Schork, A. J. & Ingason, A. (2024).
Evaluating the Joint Effects of Recurrent Copy Number Variants and Polygenic Scores on the Risk of Psychiatric Disorders in the iPSYCH2015 Case-Cohort Sample.
https://doi.org/10.1101/2024.09.23.24314234
Breinbjerg, A., Jørgensen, C. S., Walters, G. B.
, Grove, J., Als, T. D., Kamperis, K., Stéfansdóttir, L.
, Thirstrup, J. P., Borg, B., Albiñana, C., Vilhjálmsson, B. J., Eðvarðsson, V. Ö., Stefánsson, H.
, Mortensen, P. B., Agerbo, E., Werge, T.
, Børglum, A., Demontis, D., Stefánsson, K.
... Christensen, J. H. (2024).
Exploring the Genetic Risk of Childhood Daytime Urinary Incontinence: A Genome-Wide Association Study.
The Journal of Urology,
212(6), 851-861.
https://doi.org/10.1097/JU.0000000000004187
Nievergelt, C. M., Maihofer, A. X., Atkinson, E. G., Chen, C.-Y., Choi, K. W., Coleman, J. R. I., Daskalakis, N. P., Duncan, L. E., Polimanti, R., Aaronson, C., Amstadter, A. B., Andreassen, O. A., Arbisi, P. A., Ashley-Koch, A. E., Austin, S. B., Avdibegoviç, E., Babić, D., Bacanu, S.-A., Baker, D. G. ... AURORA Study (2024).
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder.
Nature Genetics,
56(5), 792-808.
https://doi.org/10.1038/s41588-024-01707-9
Johannsen, B. M. W., Larsen, J. T., Liu, X., Madsen, K. B., Maegbaek, M. L., Albiñana, C., Bergink, V.
, Laursen, T. M., Bech, B. H., Mortensen, P. B., Nordentoft, M.
, Børglum, A. D., Werge, T., Hougaard, D. M.
, Agerbo, E., Petersen, L. V. & Munk-Olsen, T. (2024).
Identification of women at high risk of postpartum psychiatric episodes: A population-based study quantifying relative and absolute risks following exposure to selected risk factors and genetic liability.
Acta Psychiatrica Scandinavica,
150(5), 385-394. Article 13622.
https://doi.org/10.1111/acps.13622
Mundy, J., Hall, A. S. M., Steinbach, J., Albinaña, C., Agerbo, E., Als, T. D., Thapar, A.
, McGrath, J. J., Vilhjálmsson, B. J., Nordentoft, M., Werge, T.
, Børglum, A., Mortensen, P. B. & Musliner, K. L. (2024).
Polygenic liabilities and treatment trajectories in early-onset depression: a Danish register-based study.
Psychological Medicine,
54(14), 3828-3837.
https://doi.org/10.1017/S0033291724002186
LaBianca, S.
, Brikell, I., Helenius, D., Loughnan, R., Mefford, J., Palmer, C. E., Walker, R., Gådin, J. R., Krebs, M., Appadurai, V., Vaez, M.
, Agerbo, E., Pedersen, M. G., Børglum, A. D., Hougaard, D. M.
, Mors, O., Nordentoft, M.
, Mortensen, P. B., Kendler, K. S. ... Schork, A. J. (2024).
Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder.
Nature Genetics,
56(2), 234-244.
https://doi.org/10.1038/s41588-023-01593-7
Jefsen, O. H., Holde, K., McGrath, J. J., Rajagopal, V. M., Albiñana, C., Vilhjálmsson, B. J., Grove, J., Agerbo, E., Yilmaz, Z., Plana-Ripoll, O., Munk-Olsen, T., Demontis, D., Børglum, A., Mors, O., Bulik, C. M.
, Mortensen, P. B. & Petersen, L. V. (2024).
Polygenic risk of mental disorders and subject-specific school grades.
Biological Psychiatry,
96(3), 222-229.
https://doi.org/10.1016/j.biopsych.2023.11.020
Vaez, M., Montalbano, S., Calle Sánchez, X., Georgii Hellberg, K.-L., Dehkordi, S. R., Krebs, M. D., Meijsen, J., Shorter, J., Bybjerg-Grauholm, J.
, Mortensen, P. B., Børglum, A. D., Hougaard, D. M., Nordentoft, M., Geschwind, D. H., Buil, A., Schork, A. J., Helenius, D., Raznahan, A., Thompson, W. K. ... iPSYCH Investigators (2024).
Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants.
JAMA Psychiatry,
81(10), 957-966. Article 10.
https://doi.org/10.1001/jamapsychiatry.2024.1453
Patel, K. H. S., Walters, G. B., Stefánsson, H., Stefánsson, K., Degenhardt, F., Nothen, M., Van Der Veen, T.
, Demontis, D., Borglum, A., Kristiansen, M., Bass, N. J. & McQuillin, A. (2024).
Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD.
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics,
195(4), Article e32967.
https://doi.org/10.1002/ajmg.b.32967
Pisanu, C., Congiu, D., Meloni, A., Paribello, P., Severino, G., Ardau, R., Chillotti, C.
, Als, T. D., Børglum, A. D., Del Zompo, M., Manchia, M. & Squassina, A. (2024).
Sex differences in shared genetic determinants between severe mental disorders and metabolic traits.
Psychiatry Research,
342, Article 116195.
https://doi.org/10.1016/j.psychres.2024.116195
Wimberley, T., Brikell, I., Astrup, A., Larsen, J. T., Petersen, L. V., Albiñana, C., Vilhjálmsson, B. J., Bulik, C. M., Chang, Z., Fanelli, G., Bralten, J., Mota, N. R., Salas-Salvadó, J., Fernandez-Aranda, F., Bulló, M., Franke, B.
, Børglum, A., Mortensen, P. B., Horsdal, H. T. & Dalsgaard, S. (2024).
Shared familial risk for type 2 diabetes mellitus and psychiatric disorders: a nationwide multigenerational genetics study.
Psychological Medicine,
54(11), 1-10.
https://doi.org/10.1017/S0033291724001053
Nielsen, T. T., Duan, J., Levey, D. F., Walters, G. B., Johnson, E. C., Thorgeirsson, T., Werge, T., Mortensen, P. B., Stefansson, H., Stefansson, K., Hougaard, D. M., Agrawal, A., Gelernter, J.
, Grove, J., Børglum, A. & Demontis, D. (2024).
Shared genetics of ADHD, cannabis use disorder and cannabis use and prediction of cannabis use disorder in ADHD.
Nature Mental Health,
2(9), 1071-1083. Article 108535.
https://doi.org/10.1038/s44220-024-00277-3
Daskalakis, N. P., Iatrou, A., Chatzinakos, C., Jajoo, A., Snijders, C., Wylie, D., DiPietro, C. P., Tsatsani, I., Chen, C.-Y., Pernia, C. D., Soliva-Estruch, M., Arasappan, D., Bharadwaj, R. A., Collado-Torres, L., Wuchty, S., Alvarez, V. E., Dammer, E. B., Deep-Soboslay, A., Duong, D. M. ... PTSD Working Group of Psychiatric Genomics Consortium** (2024).
Systems biology dissection of PTSD and MDD across brain regions, cell types, and blood.
Science,
384(6698), Article eadh3707.
https://doi.org/10.1126/science.adh3707
Petersen, L., Christiansen, G., Chatwin, H.
, Yilmaz, Z., Schendel, D., Bulik, C.
, Grove, J., Brikell, I., Semark, B., Holde, K., Abdulkadir, M., Hubel, C., Albiñana, C., Vilhjálmsson, B., Borglum, A., Demontis, D. & Mortensen, P. (2024).
The role of co-occurring conditions and genetics in the associations of eating disorders with attention-deficit/hyperactivity disorder and autism spectrum disorder. Research square
https://doi.org/10.21203/rs.3.rs-4236554/v1
Kim, S. W., Lee, H., Song, D. Y., Lee, G. H., Ji, J., Park, J. W., Han, J. H., Lee, J. W., Byun, H. J., Son, J. H., Kim, Y. R., Lee, Y., Kim, J., Jung, A., Lee, J., Kim, E., Kim, S. H., Lee, J. H., Satterstrom, F. K. ... An, J. Y. (2024).
Whole genome sequencing analysis identifies sex differences of familial pattern contributing to phenotypic diversity in autism.
Genome Medicine,
16(1), 114. Article 114.
https://doi.org/10.1186/s13073-024-01385-6
Appadurai, V., Bybjerg-Grauholm, J., Krebs, M. D., Rosengren, A., Buil, A., Ingason, A.
, Mors, O., Børglum, A. D., Hougaard, D. M., Nordentoft, M.
, Mortensen, P. B., Delaneau, O., Werge, T. & Schork, A. J. (2023).
Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks.
Communications Biology,
6(1), Article 101.
https://doi.org/10.1038/s42003-023-04477-y
Pedersen, E. M., Agerbo, E., Plana-Ripoll, O., Steinbach, J., Krebs, M. D., Hougaard, D. M., Werge, T., Nordentoft, M.
, Børglum, A. D., Musliner, K. L., Ganna, A., Schork, A. J.
, Mortensen, P. B., McGrath, J. J., Privé, F. & Vilhjálmsson, B. J. (2023).
ADuLT: An efficient and robust time-to-event GWAS.
Nature Communications,
14(1), Article 5553.
https://doi.org/10.1038/s41467-023-41210-z
Sánchez, X. C., Montalbano, S., Vaez, M., Krebs, M. D., Byberg-Grauholm, J.
, Mortensen, P. B., Børglum, A. D., Hougaard, D. M., Nordentoft, M., Geschwind, D. H., Buil, A., Schork, A. J., Thompson, W. K., Raznahan, A., Helenius, D., Werge, T. & Ingason, A. (2023).
Associations of psychiatric disorders with sex chromosome aneuploidies in the Danish iPSYCH2015 dataset: a case-cohort study.
The Lancet Psychiatry,
10(2), 129-138.
https://doi.org/10.1016/S2215-0366(23)00004-4
Als, T. D., Kurki, M. I.
, Grove, J., Voloudakis, G., Therrien, K., Tasanko, E.
, Nielsen, T. T., Naamanka, J., Veerapen, K., Levey, D. F., Bendl, J., Bybjerg-Grauholm, J., Zeng, B.
, Demontis, D., Rosengren, A., Athanasiadis, G., Bækved-Hansen, M.
, Qvist, P., Bragi Walters, G.
... Børglum, A. D. (2023).
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.
Nature Medicine,
29(7), 1832-1844.
https://doi.org/10.1038/s41591-023-02352-1
Nievergelt, C. M., Maihofer, A. X., Atkinson, E. G., Chen, C.-Y., Choi, K. W., Coleman, J. R., Daskalakis, N. P., Duncan, L. E., Polimanti, R., Aaronson, C., Amstadter, A. B.
, Andersen, S. B., Andreassen, O. A., Arbisi, P. A., Ashley-Koch, A. E., Austin, S. B., Avdibegoviç, E., Babic, D., Bacanu, S.-A. ... Koenen, K. C. (2023).
Discovery of 95 PTSD loci provides insight into genetic architecture and neurobiology of trauma and stress-related disorders. medRxiv.
https://doi.org/10.1101/2023.08.31.23294915
Ribasés, M., Mitjans, M., Hartman, C. A., Soler Artigas, M.
, Demontis, D., Larsson, H., Ramos-Quiroga, J. A., Kuntsi, J., Faraone, S. V.
, Børglum, A. D., Reif, A., Franke, B. & Cormand, B. (2023).
Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes.
Neuroscience and Biobehavioral Reviews,
153, Article 105313.
https://doi.org/10.1016/j.neubiorev.2023.105313
Albiñana, C., Zhu, Z., Borbye-Lorenzen, N., Boelt, S. G., Cohen, A. S., Skogstrand, K., Wray, N. R., Revez, J. A.
, Privé, F., Petersen, L. V., Bulik, C. M.
, Plana-Ripoll, O., Musliner, K. L., Agerbo, E., Børglum, A. D., Hougaard, D. M., Nordentoft, M., Werge, T.
, Mortensen, P. B. ... McGrath, J. J. (2023).
Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots.
Nature Communications,
14(1), Article 852.
https://doi.org/10.1038/s41467-023-36392-5
Bang Madsen, K., Liu, X., Albiñana, C., Jóhann Vilhjálmsson, B., Agerbo, E., Mortensen, P. B., Hougaard, D. M., Nordentoft, M., Werge, T.
, Mors, O., Børglum, A. D. & Munk-Olsen, T. (2023).
Genetic liability to posttraumatic stress disorder and its association with postpartum depression.
Psychological Medicine,
53(11), 5052-5059.
https://doi.org/10.1017/S0033291722002045
Demontis, D., Walters, G. B., Athanasiadis, G., Walters, R., Therrien, K.
, Nielsen, T. T., Farajzadeh, L., Voloudakis, G., Bendl, J., Zeng, B., Zhang, W.
, Grove, J., Als, T. D., Duan, J., Satterstrom, F. K., Bybjerg-Grauholm, J., Bækved-Hansen, M., Gudmundsson, O. O., Magnusson, S. H. ... ADHD Working Group of the Psychiatric Genomics Consortium (2023).
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.
Nature Genetics,
55(2), 198-208.
https://doi.org/10.1038/s41588-022-01285-8
Rajagopal, V. M., Ganna, A., Coleman, J. R. I., Allegrini, A., Voloudakis, G.
, Grove, J., Als, T. D., Horsdal, H. T., Petersen, L., Appadurai, V., Schork, A., Buil, A., Bulik, C. M., Bybjerg-Grauholm, J., Bækvad-Hansen, M., Hougaard, D. M.
, Mors, O., Nordentoft, M., Werge, T.
... Demontis, D. (2023).
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity.
Scientific Reports,
13, Article 429.
https://doi.org/10.1038/s41598-022-26845-0
Docherty, A. R., Mullins, N., Ashley-Koch, A. E., Qin, X., Coleman, J. R. I., Shabalin, A., Kang, J. E., Murnyak, B., Wendt, F., Adams, M., Campos, A. I., DiBlasi, E., Fullerton, J. M., Kranzler, H. R., Bakian, A. V., Monson, E. T., Rentería, M. E., Walss-Bass, C., Andreassen, O. A. ... Ruderfer, D. M. (2023).
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.
American Journal of Psychiatry,
180(10), 723-738.
https://doi.org/10.1176/appi.ajp.21121266
Brikell, I., Wimberley, T., Albiñana, C., Vilhjálmsson, B. J., Agerbo, E., Børglum, A. D., Demontis, D., Schork, A. J., LaBianca, S., Werge, T., Hougaard, D. M., Nordentoft, M.
, Mors, O., Mortensen, P. B., Petersen, L. V. & Dalsgaard, S. (2023).
Interplay of ADHD Polygenic Liability With Birth-Related, Somatic, and Psychosocial Factors in ADHD: A Nationwide Study.
The American Journal of Psychiatry (Spanish Edition),
180(1), 73-88.
https://doi.org/10.1176/appi.ajp.21111105
Levey, D. F., Galimberti, M., Deak, J. D., Wendt, F. R., Bhattacharya, A., Koller, D., Harrington, K. M., Quaden, R., Johnson, E. C., Gupta, P., Biradar, M., Lam, M., Cooke, M.
, Rajagopal, V. M., Empke, S. L. L., Zhou, H., Nunez, Y. Z., Kranzler, H. R., Edenberg, H. J. ... Veterans Affairs Million Veteran Program (2023).
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications.
Nature Genetics,
55(12), 2094-2103.
https://doi.org/10.1038/s41588-023-01563-z
Zhou, H., Kember, R. L., Deak, J. D., Xu, H., Toikumo, S., Yuan, K., Lind, P. A.
, Farajzadeh, L., Wang, L., Hatoum, A. S., Johnson, J., Lee, H., Mallard, T. T., Xu, J., Johnston, K. J. A., Johnson, E. C.
, Nielsen, T. T., Galimberti, M., Dao, C. ... Million Veteran Program (2023).
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals.
Nature Medicine,
29(12), 3184-3192.
https://doi.org/10.1038/s41591-023-02653-5
Albiñana, C., Zhu, Z., Schork, A. J., Ingason, A., Aschard, H.
, Brikell, I., Bulik, C. M.
, Petersen, L. V., Agerbo, E., Grove, J., Nordentoft, M., Hougaard, D. M., Werge, T.
, Børglum, A. D., Mortensen, P. B., McGrath, J. J., Neale, B. M.
, Privé, F. & Vilhjálmsson, B. J. (2023).
Multi-PGS enhances polygenic prediction by combining 937 polygenic scores.
Nature Communications,
14(1), Article 4702.
https://doi.org/10.1038/s41467-023-40330-w
Rolland, T., Cliquet, F., Anney, R. J. L., Moreau, C., Traut, N., Mathieu, A., Huguet, G.
, Duan, J., Warrier, V., Portalier, S., Dry, L., Leblond, C. S., Douard, E., Amsellem, F., Malesys, S., Maruani, A., Toro, R.
, Børglum, A. D., Grove, J. ... Bourgeron, T. (2023).
Phenotypic effects of genetic variants associated with autism.
Nature Medicine,
29(7), 1671-1680.
https://doi.org/10.1038/s41591-023-02408-2
Musliner, K. L., Andersen, K. K.
, Agerbo, E., Albiñana, C., Vilhjalmsson, B. J., Rajagopal, V. M., Bybjerg-Grauholm, J., Bækved-Hansen, M.
, Pedersen, C. B., Pedersen, M. G., Munk-Olsen, T., Benros, M. E.
, Als, T. D., Grove, J., Werge, T.
, Børglum, A. D., Hougaard, D. M.
, Mors, O., Nordentoft, M. ... Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2023).
Polygenic liability, stressful life events and risk for secondary-treated depression in early life: a nationwide register-based case-cohort study.
Psychological Medicine,
53(1), 217-226.
https://doi.org/10.1017/S0033291721001410
Wang, X., Walker, A., Revez, J. A., Ni, G., Adams, M. J., McIntosh, A. M. & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2023).
Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability.
American Journal of Human Genetics,
110(7), 1207-1215.
https://doi.org/10.1016/j.ajhg.2023.06.006
Munk-Olsen, T., Di Florio, A.
, Madsen, K. B., Albiñana, C., Mægbæk, M. L., Bergink, V., Frøkjær, V. G.
, Agerbo, E., Vilhjálmsson, B. J., Werge, T., Nordentoft, M., Hougaard, D. M.
, Børglum, A. D., Mors, O., Mortensen, P. B. & Liu, X. (2023).
Postpartum and non-postpartum depression: a population-based matched case-control study comparing polygenic risk scores for severe mental disorders.
Translational Psychiatry,
13(1), Article 346.
https://doi.org/10.1038/s41398-023-02649-2
Sørensen, H. J.
, Antonsen, S., Benros, M. E., Erlangsen, A.
, Albiñana, C., Nordentoft, M.
, Børglum, A. D., Mors, O., Werge, T.
, Mortensen, P. B., Hougaard, D., Webb, R. T.
& Agerbo, E. (2023).
School performance and genetic propensities for educational attainment and depression in the etiology of self-harm: a Danish population-based study.
Nordic Journal of Psychiatry,
77(2), 179-187.
https://doi.org/10.1080/08039488.2022.2078998
Borbye-Lorenzen, N.
, Zhu, Z., Agerbo, E., Albiñana, C., Benros, M. E., Bian, B.
, Børglum, A. D., Bulik, C. M.
, Debost, J.-C. P. G., Grove, J., Hougaard, D. M., McRae, A. F.
, Mors, O., Mortensen, P. B., Musliner, K. L., Nordentoft, M.
, Petersen, L. V., Privé, F., Sidorenko, J.
... McGrath, J. J. (2023).
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders.
Cell Genomics,
3(12), 100457. Article 100457.
https://doi.org/10.1016/j.xgen.2023.100457