My Bibliography

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Campbell ML, Odokonyero R, Akena D, Alemayehu M, Atwoli L, Chibnik LB, Gelaye B, Gichuru S, Kariuki SM, Koenen KC, Kwobah E, Kyebuzibwa J, Mwema RM, Newton CRJC, Post K, Pretorius A, Stevenson A, Stroud RE 2nd, Teferra S, Zingela Z, Stein DJ, Hook K. Sociodemographic influences on substance use in psychosis in an African cohort. Schizophr Res. 2025 Jul;281:157-163. doi: 10.1016/j.schres.2025.04.012. Epub 2025 May 10. PubMed PMID: 40349466.

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Mandla R, Shi Z, Hou K, Wang Y, Mies G, Aw AJ, Cullina S, Kenny E, Atkinson E, Martin AR, Pasaniuc B. Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences. medRxiv. 2025 Apr 3;. doi: 10.1101/2025.04.02.25325115. PubMed PMID: 40236441; PubMed Central PMCID: PMC11998848.

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Lin YS, Tan T, Wang Y, Pasaniuc B, Martin AR, Atkinson EG. Differential performance of polygenic prediction across traits and populations depending on genotype discovery approach. bioRxiv. 2025 Mar 18;. doi: 10.1101/2025.03.18.644029. PubMed PMID: 40166153; PubMed Central PMCID: PMC11957064.

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Jee YH, Wang Y, Jung KJ, Lee JY, Kimm H, Duan R, Price AL, Martin AR, Kraft P. Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminate their genetic architectures. medRxiv. 2025 Jan 7;. doi: 10.1101/2024.05.17.24307550. PubMed PMID: 38798434; PubMed Central PMCID: PMC11118625.

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Yared M, Kim HH, Ametaj A, Alemayehu M, Stevenson A, Milkias B, Girma E, Gelaye B, Teferra S. An Item Response Theory Analysis of the Psychosis Screening Questionnaire in Ethiopia. Early Interv Psychiatry. 2025 Jan;19(1):e13609. doi: 10.1111/eip.13609. Epub 2024 Sep 2. PubMed PMID: 39223760; PubMed Central PMCID: PMC11729251.

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Kisiang'ani IB, Aden M, Mwangi HR, Akena D, Alemayehu M, Barasa J, Gelaye B, Gichuru S, Kariuki SM, Kwobah EK, Kyebuzibwa J, Mwema RM, Newton CRJC, Ongeri L, Pretorius A, Stein DJ, Stevenson A, Stroud RE 2nd, Teferra S, Zingela Z, Atwoli L. Exploring psychotic symptoms among substance-naïve individuals and recent abstainers without a psychosis diagnosis: A cross-country study across Kenya, Uganda, Ethiopia, and South Africa. Psychiatry Res. 2024 Dec;342:116253. doi: 10.1016/j.psychres.2024.116253. Epub 2024 Oct 28. PubMed PMID: 39514937.

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Kipkemoi P, Mufford MS, Akena D, Alemayehu M, Atwoli L, Chibnik LB, Gelaye B, Gichuru S, Kariuki SM, Koenen KC, Kwobah E, Kyebuzibwa J, Mwema RM, Newton CRJC, Pretorius A, Stein DJ, Stevenson A, Stroud RE 2nd, Teferra S, Zingela Z, Post K, Korte KJ. Evaluation of the psychometric properties of the UBACC questionnaire in a multi-country psychiatric study in Africa. Compr Psychiatry. 2024 Nov;135:152526. doi: 10.1016/j.comppsych.2024.152526. Epub 2024 Aug 26. PubMed PMID: 39208558; NIHMSID:NIHMS2025069.

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Tindi KBB, Kalungi A, Kinyanda E, Gelaye B, Martin AR, Galiwango R, Ssembajjwe W, Kirumira F, Pretorius A, Stevenson A, Newton CRJC, Stein DJ, Atkinson EG, Mwesiga EK, Kyebuzibwa J, Chibnik LB, Atwoli L, Baker M, Alemayehu M, Mwende RM, Stroud RE, Teferra S, Gichuru S, Kariuki SM, Zingela Z, Nyirenda M, Fatumo S, Akena DH. Psychological Distress Among Ethnically Diverse Participants From Eastern and Southern Africa. JAMA Netw Open. 2024 Oct 1;7(10):e2438304. doi: 10.1001/jamanetworkopen.2024.38304. PubMed PMID: 39382897; PubMed Central PMCID: PMC11581619.

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Choi KW, Tubbs JD, Lee YH, He Y, Tsuo K, Yohannes MT, Nkambule LL, Madsen E, Ghimire DJ, Hermosilla S, Ge T, Martin AR, Axinn WG, Smoller JW. Genetic architecture and socio-environmental risk factors for major depressive disorder in Nepal. Psychol Med. 2024 Aug;54(11):3126-3134. doi: 10.1017/S0033291724001284. Epub 2024 Sep 16. PubMed PMID: 39282852; PubMed Central PMCID: PMC12050005.

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He Y, Lu W, Jee YH, Wang Y, Tsuo K, Qian DC, Diao JA, Huang H, Patel CJ, Byun J, Pasaniuc B, Atkinson EG, Amos CI, Moll M, Cho MH, Martin AR. Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction. medRxiv. 2024 Sep 10;. doi: 10.1101/2024.08.25.24312558. PubMed PMID: 39252935; PubMed Central PMCID: PMC11383478.

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Boltz TA, Chu BB, Liao C, Sealock JM, Ye R, Majara L, Fu JM, Service S, Zhan L, Medland SE, Chapman SB, Rubinacci S, DeFelice M, Grimsby JL, Abebe T, Alemayehu M, Ashaba FK, Atkinson EG, Bigdeli T, Bradway AB, Brand H, Chibnik LB, Fekadu A, Gatzen M, Gelaye B, Gichuru S, Gildea ML, Hill TC, Huang H, Hubbard KM, Injera WE, James R, Joloba M, Kachulis C, Kalmbach PR, Kamulegeya R, Kigen G, Kim S, Koen N, Kwobah EK, Kyebuzibwa J, Lee S, Lennon NJ, Lind PA, Lopera-Maya EA, Makale J, Mangul S, McMahon J, Mowlem P, Musinguzi H, Mwema RM, Nakasujja N, Newman CP, Nkambule LL, O'Neil CR, Olivares AM, Olsen CM, Ongeri L, Parsa SJ, Pretorius A, Ramesar R, Reagan FL, Sabatti C, Schneider JA, Shiferaw W, Stevenson A, Stricker E, Stroud RE 2nd, Tang J, Whiteman D, Yohannes MT, Yu M, Yuan K, Akena D, Atwoli L, Kariuki SM, Koenen KC, Newton CRJC, Stein DJ, Teferra S, Zingela Z, Pato CN, Pato MT, Lopez-Jaramillo C, Freimer N, Ophoff RA, Olde Loohuis LM, Talkowski ME, Neale BM, Howrigan DP, Martin AR. A blended genome and exome sequencing method captures genetic variation in an unbiased, high-quality, and cost-effective manner. bioRxiv. 2024 Sep 8;. doi: 10.1101/2024.09.06.611689. PubMed PMID: 39282356; PubMed Central PMCID: PMC11398523.

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Tsuo K, Shi Z, Ge T, Mandla R, Hou K, Ding Y, Pasaniuc B, Wang Y, Martin AR. All of Us diversity and scale improve polygenic prediction contextually with greatest improvements for under-represented populations. bioRxiv. 2024 Aug 6;. doi: 10.1101/2024.08.06.606846. PubMed PMID: 39149254; PubMed Central PMCID: PMC11326295.

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Stevenson A, Misra S, Girma E, Isvoranu AM, Akena D, Alemayehu M, Atwoli L, Gelaye B, Gichuru S, Kariuki SM, Kwobah EK, Kyebuzibwa J, Mwema RM, Newman CP, Newton CRJC, Ongeri L, Stroud RE 2nd, Teferra S, Koenen KC, Seedat S. Relationships between trauma types and psychotic symptoms: A network analysis of patients with psychotic disorders in a large, multi-country study in East Africa. Compr Psychiatry. 2024 Aug;133:152504. doi: 10.1016/j.comppsych.2024.152504. Epub 2024 May 31. PubMed PMID: 38876004; PubMed Central PMCID: PMC11253580.

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DeFelice M, Grimsby JL, Howrigan D, Yuan K, Chapman SB, Stevens C, DeLuca S, Townsend M, Buxbaum J, Pericak-Vance M, Qin S, Stein DJ, Teferra S, Xavier RJ, Huang H, Martin AR, Neale BM. Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays. bioRxiv. 2024 Jul 30;. doi: 10.1101/2024.04.03.587209. PubMed PMID: 38645052; PubMed Central PMCID: PMC11030253.

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Koenig Z, Yohannes MT, Nkambule LL, Zhao X, Goodrich JK, Kim HA, Wilson MW, Tiao G, Hao SP, Sahakian N, Chao KR, Walker MA, Lyu Y, Rehm HL, Neale BM, Talkowski ME, Daly MJ, Brand H, Karczewski KJ, Atkinson EG, Martin AR. A harmonized public resource of deeply sequenced diverse human genomes. Genome Res. 2024 Jun 25;34(5):796-809. doi: 10.1101/gr.278378.123. PubMed PMID: 38749656; PubMed Central PMCID: PMC11216312.

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Diao JA, He Y, Khazanchi R, Nguemeni Tiako MJ, Witonsky JI, Pierson E, Rajpurkar P, Elhawary JR, Melas-Kyriazi L, Yen A, Martin AR, Levy S, Patel CJ, Farhat M, Borrell LN, Cho MH, Silverman EK, Burchard EG, Manrai AK. Implications of Race Adjustment in Lung-Function Equations. N Engl J Med. 2024 Jun 13;390(22):2083-2097. doi: 10.1056/NEJMsa2311809. Epub 2024 May 19. PubMed PMID: 38767252; PubMed Central PMCID: PMC11305821.

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Jermy B, Läll K, Wolford BN, Wang Y, Zguro K, Cheng Y, Kanai M, Kanoni S, Yang Z, Hartonen T, Monti R, Wanner J, Youssef O, Lippert C, van Heel D, Okada Y, McCartney DL, Hayward C, Marioni RE, Furini S, Renieri A, Martin AR, Neale BM, Hveem K, Mägi R, Palotie A, Heyne H, Mars N, Ganna A, Ripatti S. A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk. Nat Commun. 2024 Jun 12;15(1):5007. doi: 10.1038/s41467-024-48938-2. PubMed PMID: 38866767; PubMed Central PMCID: PMC11169548.

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Kim B, Kim DS, Shin JG, Leem S, Cho M, Kim H, Gu KN, Seo JY, You SW, Martin AR, Park SG, Kim Y, Jeong C, Kang NG, Won HH. Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color. Nat Commun. 2024 Jun 7;15(1):4874. doi: 10.1038/s41467-024-49031-4. PubMed PMID: 38849341; PubMed Central PMCID: PMC11161515.

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Ametaj AA, Denckla CA, Stevenson A, Stroud RE 2nd, Hall J, Ongeri L, Milkias B, Hoffman J, Naisanga M, Akena D, Kyebuzibwa J, Kwobah EK, Atwoli L, Gichuru S, Teferra S, Alemayehu M, Zingela Z, Stein DJ, Pretorius A, Newton CRJC, Mwema RM, Kariuki SM, Koenen KC, Gelaye B. Cross-cultural equivalence of the Kessler Psychological Distress Scale (K10) across four African countries in a multi-national study of adults. SSM Ment Health. 2024 Jun;5. doi: 10.1016/j.ssmmh.2024.100300. Epub 2024 Feb 10. PubMed PMID: 38706931; PubMed Central PMCID: PMC11064105.

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Wang Y, He Y, Shi Y, Qian DC, Gray KJ, Winn R, Martin AR. Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds. Am J Hum Genet. 2024 May 2;111(5):809-824. doi: 10.1016/j.ajhg.2024.04.002. Epub 2024 Apr 19. Review. PubMed PMID: 38642557; PubMed Central PMCID: PMC11080611.

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Ciobanu O, He Y, Martin AR, Remick JS, Shelton JW, Eng TY, Qian DC. Patterns of Undertreatment and Overtreatment in Adjuvant Radiotherapy for Early-Stage Endometrial Cancer Based on Molecular Classification. JAMA Oncol. 2024 May 1;10(5):671-674. doi: 10.1001/jamaoncol.2024.0104. PubMed PMID: 38483373; PubMed Central PMCID: PMC10941016.

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Truong B, Hull LE, Ruan Y, Huang QQ, Hornsby W, Martin H, van Heel DA, Wang Y, Martin AR, Lee SH, Natarajan P. Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. Cell Genom. 2024 Apr 10;4(4):100523. doi: 10.1016/j.xgen.2024.100523. Epub 2024 Mar 19. PubMed PMID: 38508198; PubMed Central PMCID: PMC11019356.

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Koenig Z, Yohannes MT, Nkambule LL, Zhao X, Goodrich JK, Kim HA, Wilson MW, Tiao G, Hao SP, Sahakian N, Chao KR, Walker MA, Lyu Y, Rehm HL, Neale BM, Talkowski ME, Daly MJ, Brand H, Karczewski KJ, Atkinson EG, Martin AR. A harmonized public resource of deeply sequenced diverse human genomes. bioRxiv. 2024 Feb 28;. doi: 10.1101/2023.01.23.525248. PubMed PMID: 36747613; PubMed Central PMCID: PMC9900804.

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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, Sanna S, Nolte IM, Okada Y, Ingold N, MacGregor S, Snieder H, Surakka I, Shortt J, Gignoux C, Rafaels N, Crooks K, Verma A, Verma SS, Guare L, Rader DJ, Willer C, Martin AR, Brantley MA Jr, Gamazon ER, Jansonius NM, Joos K, Cox NJ, Hirbo J. Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. Cell Rep Med. 2024 Feb 20;5(2):101430. doi: 10.1016/j.xcrm.2024.101430. PubMed PMID: 38382466; PubMed Central PMCID: PMC10897632.

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Chen S, Francioli LC, Goodrich JK, Collins RL, Kanai M, Wang Q, Alföldi J, Watts NA, Vittal C, Gauthier LD, Poterba T, Wilson MW, Tarasova Y, Phu W, Grant R, Yohannes MT, Koenig Z, Farjoun Y, Banks E, Donnelly S, Gabriel S, Gupta N, Ferriera S, Tolonen C, Novod S, Bergelson L, Roazen D, Ruano-Rubio V, Covarrubias M, Llanwarne C, Petrillo N, Wade G, Jeandet T, Munshi R, Tibbetts K, O'Donnell-Luria A, Solomonson M, Seed C, Martin AR, Talkowski ME, Rehm HL, Daly MJ, Tiao G, Neale BM, MacArthur DG, Karczewski KJ. Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes. Nature. 2024 Feb;626(7997):E1. doi: 10.1038/s41586-024-07050-7. PubMed PMID: 38225470.

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He Y, Martin AR. We need more-diverse biobanks to improve behavioural genetics. Nat Hum Behav. 2024 Feb;8(2):197-200. doi: 10.1038/s41562-023-01795-3. PubMed PMID: 38158402.

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Chen S, Francioli LC, Goodrich JK, Collins RL, Kanai M, Wang Q, Alföldi J, Watts NA, Vittal C, Gauthier LD, Poterba T, Wilson MW, Tarasova Y, Phu W, Grant R, Yohannes MT, Koenig Z, Farjoun Y, Banks E, Donnelly S, Gabriel S, Gupta N, Ferriera S, Tolonen C, Novod S, Bergelson L, Roazen D, Ruano-Rubio V, Covarrubias M, Llanwarne C, Petrillo N, Wade G, Jeandet T, Munshi R, Tibbetts K, O'Donnell-Luria A, Solomonson M, Seed C, Martin AR, Talkowski ME, Rehm HL, Daly MJ, Tiao G, Neale BM, MacArthur DG, Karczewski KJ. A genomic mutational constraint map using variation in 76,156 human genomes. Nature. 2024 Jan;625(7993):92-100. doi: 10.1038/s41586-023-06045-0. Epub 2023 Dec 6. PubMed PMID: 38057664; PubMed Central PMCID: PMC11629659.

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Guo MH, Francioli LC, Stenton SL, Goodrich JK, Watts NA, Singer-Berk M, Groopman E, Darnowsky PW, Solomonson M, Baxter S, Tiao G, Neale BM, Hirschhorn JN, Rehm HL, Daly MJ, O'Donnell-Luria A, Karczewski KJ, MacArthur DG, Samocha KE. Inferring compound heterozygosity from large-scale exome sequencing data. Nat Genet. 2024 Jan;56(1):152-161. doi: 10.1038/s41588-023-01608-3. Epub 2023 Dec 6. PubMed PMID: 38057443; PubMed Central PMCID: PMC10872287.

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He Y, Qian DC, Diao JA, Cho MH, Silverman EK, Gusev A, Manrai AK, Martin AR, Patel CJ. Prediction and stratification of longitudinal risk for chronic obstructive pulmonary disease across smoking behaviors. Nat Commun. 2023 Dec 14;14(1):8297. doi: 10.1038/s41467-023-44047-8. PubMed PMID: 38097585; PubMed Central PMCID: PMC10721891.

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Korte KJ, Jaguga F, Kim HH, Stroud RE, Stevenson A, Akena D, Atwoli L, Gichuru S, James R, Kwobah E, Kariuki SM, Kyebuzibwa J, Mwema RM, Newton CRJC, Zingela Z, Stein DJ, Alemayehu M, Teferra S, Koenen KC, Gelaye B. Psychometric properties of the mini international neuropsychiatric interview (MINI) psychosis module: a Sub-Saharan Africa cross country comparison. Psychol Med. 2023 Nov;53(15):7042-7052. doi: 10.1017/S0033291723000296. Epub 2023 Mar 10. PubMed PMID: 36896802; PubMed Central PMCID: PMC10492890.

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Koyama S, Wang Y, Paruchuri K, Uddin MM, Cho SMJ, Urbut SM, Haidermota S, Hornsby WE, Green RC, Daly MJ, Neale BM, Ellinor PT, Smoller JW, Lebo MS, Karlson EW, Martin AR, Natarajan P. Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. medRxiv. 2023 Oct 25;. doi: 10.1101/2023.10.24.23297096. PubMed PMID: 37961173; PubMed Central PMCID: PMC10635180.

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Wang Y, Kanai M, Tan T, Kamariza M, Tsuo K, Yuan K, Zhou W, Okada Y, Huang H, Turley P, Atkinson EG, Martin AR. Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. Cell Genom. 2023 Oct 11;3(10):100408. doi: 10.1016/j.xgen.2023.100408. eCollection 2023 Oct 11. PubMed PMID: 37868036; PubMed Central PMCID: PMC10589629.

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A second update on mapping the human genetic architecture of COVID-19. Nature. 2023 Sep;621(7977):E7-E26. doi: 10.1038/s41586-023-06355-3. Epub 2023 Sep 6. PubMed PMID: 37674002; PubMed Central PMCID: PMC10482689.

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Majara L, Kalungi A, Koen N, Tsuo K, Wang Y, Gupta R, Nkambule LL, Zar H, Stein DJ, Kinyanda E, Atkinson EG, Martin AR. Low and differential polygenic score generalizability among African populations due largely to genetic diversity. HGG Adv. 2023 Apr 13;4(2):100184. doi: 10.1016/j.xhgg.2023.100184. eCollection 2023 Apr 13. PubMed PMID: 36873096; PubMed Central PMCID: PMC9982687.

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He Y, Qian DC, Diao JA, Cho MH, Silverman EK, Gusev A, Manrai AK, Martin AR, Patel CJ. Prediction and stratification of longitudinal risk for chronic obstructive pulmonary disease across smoking behaviors. medRxiv. 2023 Apr 5;. doi: 10.1101/2023.04.04.23288086. PubMed PMID: 37066248; PubMed Central PMCID: PMC10104210.

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Truong B, Hull LE, Ruan Y, Huang QQ, Hornsby W, Martin H, van Heel DA, Wang Y, Martin AR, Lee SH, Natarajan P. Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. medRxiv. 2023 Mar 23;. doi: 10.1101/2023.02.21.23286110. PubMed PMID: 36865265; PubMed Central PMCID: PMC9980241.

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Meyer MN, Appelbaum PS, Benjamin DJ, Callier SL, Comfort N, Conley D, Freese J, Garrison NA, Hammonds EM, Harden KP, Lee SS, Martin AR, Martschenko DO, Neale BM, Palmer RHC, Tabery J, Turkheimer E, Turley P, Parens E. Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility. Hastings Cent Rep. 2023 Mar;53 Suppl 1(Suppl 1):S2-S49. doi: 10.1002/hast.1477. PubMed PMID: 37078667; PubMed Central PMCID: PMC10433733.

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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, Smoller JW, Uzunovic J, Wolford BN, Willer C, Gamazon ER, Cox NJ, Surakka I, Okada Y, Martin AR, Hirbo J. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts. Cell Genom. 2023 Jan 11;3(1):100241. doi: 10.1016/j.xgen.2022.100241. eCollection 2023 Jan 11. PubMed PMID: 36777179; PubMed Central PMCID: PMC9903818.

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Tsuo K, Zhou W, Wang Y, Kanai M, Namba S, Gupta R, Majara L, Nkambule LL, Morisaki T, Okada Y, Neale BM, Daly MJ, Martin AR. Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. Cell Genom. 2022 Dec 14;2(12):100212. doi: 10.1016/j.xgen.2022.100212. eCollection 2022 Dec 14. PubMed PMID: 36778051; PubMed Central PMCID: PMC9903683.

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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, Kurki M, Maasha M, Brumpton BM, Chavan S, Chen TT, Daya M, Ding Y, Feng YA, Guare LA, Gignoux CR, Graham SE, Hornsby WE, Ingold N, Ismail SI, Johnson R, Laisk T, Lin K, Lv J, Millwood IY, Moreno-Grau S, Nam K, Palta P, Pandit A, Preuss MH, Saad C, Setia-Verma S, Thorsteinsdottir U, Uzunovic J, Verma A, Zawistowski M, Zhong X, Afifi N, Al-Dabhani KM, Al Thani A, Bradford Y, Campbell A, Crooks K, de Bock GH, Damrauer SM, Douville NJ, Finer S, Fritsche LG, Fthenou E, Gonzalez-Arroyo G, Griffiths CJ, Guo Y, Hunt KA, Ioannidis A, Jansonius NM, Konuma T, Lee MTM, Lopez-Pineda A, Matsuda Y, Marioni RE, Moatamed B, Nava-Aguilar MA, Numakura K, Patil S, Rafaels N, Richmond A, Rojas-Muñoz A, Shortt JA, Straub P, Tao R, Vanderwerff B, Vernekar M, Veturi Y, Barnes KC, Boezen M, Chen Z, Chen CY, Cho J, Smith GD, Finucane HK, Franke L, Gamazon ER, Ganna A, Gaunt TR, Ge T, Huang H, Huffman J, Katsanis N, Koskela JT, Lajonchere C, Law MH, Li L, Lindgren CM, Loos RJF, MacGregor S, Matsuda K, Olsen CM, Porteous DJ, Shavit JA, Snieder H, Takano T, Trembath RC, Vonk JM, Whiteman DC, Wicks SJ, Wijmenga C, Wright J, Zheng J, Zhou X, Awadalla P, Boehnke M, Bustamante CD, Cox NJ, Fatumo S, Geschwind DH, Hayward C, Hveem K, Kenny EE, Lee S, Lin YF, Mbarek H, Mägi R, Martin HC, Medland SE, Okada Y, Palotie AV, Pasaniuc B, Rader DJ, Ritchie MD, Sanna S, Smoller JW, Stefansson K, van Heel DA, Walters RG, Zöllner S, Martin AR, Willer CJ, Daly MJ, Neale BM. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genom. 2022 Oct 12;2(10):100192. doi: 10.1016/j.xgen.2022.100192. eCollection 2022 Oct 12. PubMed PMID: 36777996; PubMed Central PMCID: PMC9903716.

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Atkinson EG, Dalvie S, Pichkar Y, Kalungi A, Majara L, Stevenson A, Abebe T, Akena D, Alemayehu M, Ashaba FK, Atwoli L, Baker M, Chibnik LB, Creanza N, Daly MJ, Fekadu A, Gelaye B, Gichuru S, Injera WE, James R, Kariuki SM, Kigen G, Koen N, Koenen KC, Koenig Z, Kwobah E, Kyebuzibwa J, Musinguzi H, Mwema RM, Neale BM, Newman CP, Newton CRJC, Ongeri L, Ramachandran S, Ramesar R, Shiferaw W, Stein DJ, Stroud RE, Teferra S, Yohannes MT, Zingela Z, Martin AR. Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa. Am J Hum Genet. 2022 Sep 1;109(9):1667-1679. doi: 10.1016/j.ajhg.2022.07.013. PubMed PMID: 36055213; PubMed Central PMCID: PMC9502052.

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Kullo IJ, Lewis CM, Inouye M, Martin AR, Ripatti S, Chatterjee N. Polygenic scores in biomedical research. Nat Rev Genet. 2022 Sep;23(9):524-532. doi: 10.1038/s41576-022-00470-z. Epub 2022 Mar 30. PubMed PMID: 35354965; PubMed Central PMCID: PMC9391275.

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Wang Y, Tsuo K, Kanai M, Neale BM, Martin AR. Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores. Annu Rev Biomed Data Sci. 2022 Aug 10;5:293-320. doi: 10.1146/annurev-biodatasci-111721-074830. Epub 2022 May 16. Review. PubMed PMID: 35576555; PubMed Central PMCID: PMC9828290.

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A first update on mapping the human genetic architecture of COVID-19. Nature. 2022 Aug;608(7921):E1-E10. doi: 10.1038/s41586-022-04826-7. Epub 2022 Aug 3. PubMed PMID: 35922517; PubMed Central PMCID: PMC9352569.

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Ruan Y, Lin YF, Feng YA, Chen CY, Lam M, Guo Z, He L, Sawa A, Martin AR, Qin S, Huang H, Ge T. Author Correction: Improving polygenic prediction in ancestrally diverse populations. Nat Genet. 2022 Aug;54(8):1259. doi: 10.1038/s41588-022-01144-6. PubMed PMID: 35789324.

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Kousathanas A, Pairo-Castineira E, Rawlik K, Stuckey A, Odhams CA, Walker S, Russell CD, Malinauskas T, Wu Y, Millar J, Shen X, Elliott KS, Griffiths F, Oosthuyzen W, Morrice K, Keating S, Wang B, Rhodes D, Klaric L, Zechner M, Parkinson N, Siddiq A, Goddard P, Donovan S, Maslove D, Nichol A, Semple MG, Zainy T, Maleady-Crowe F, Todd L, Salehi S, Knight J, Elgar G, Chan G, Arumugam P, Patch C, Rendon A, Bentley D, Kingsley C, Kosmicki JA, Horowitz JE, Baras A, Abecasis GR, Ferreira MAR, Justice A, Mirshahi T, Oetjens M, Rader DJ, Ritchie MD, Verma A, Fowler TA, Shankar-Hari M, Summers C, Hinds C, Horby P, Ling L, McAuley D, Montgomery H, Openshaw PJM, Elliott P, Walsh T, Tenesa A, Fawkes A, Murphy L, Rowan K, Ponting CP, Vitart V, Wilson JF, Yang J, Bretherick AD, Scott RH, Hendry SC, Moutsianas L, Law A, Caulfield MJ, Baillie JK. Whole-genome sequencing reveals host factors underlying critical COVID-19. Nature. 2022 Jul;607(7917):97-103. doi: 10.1038/s41586-022-04576-6. Epub 2022 Mar 7. PubMed PMID: 35255492; PubMed Central PMCID: PMC9259496.

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Martin AR, Stroud RE 2nd, Abebe T, Akena D, Alemayehu M, Atwoli L, Chapman SB, Flowers K, Gelaye B, Gichuru S, Kariuki SM, Kinyanjui S, Korte KJ, Koen N, Koenen KC, Newton CRJC, Olivares AM, Pollock S, Post K, Singh I, Stein DJ, Teferra S, Zingela Z, Chibnik LB. Increasing diversity in genomics requires investment in equitable partnerships and capacity building. Nat Genet. 2022 Jun;54(6):740-745. doi: 10.1038/s41588-022-01095-y. PubMed PMID: 35668301; PubMed Central PMCID: PMC7613571.

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Ruan Y, Lin YF, Feng YA, Chen CY, Lam M, Guo Z, He L, Sawa A, Martin AR, Qin S, Huang H, Ge T. Improving polygenic prediction in ancestrally diverse populations. Nat Genet. 2022 May;54(5):573-580. doi: 10.1038/s41588-022-01054-7. Epub 2022 May 5. PubMed PMID: 35513724; PubMed Central PMCID: PMC9117455.

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Bitta M, Thungana Y, Kim HH, Denckla CA, Ametaj A, Yared M, Kwagala C, Ongeri L, Stroud RE, Kwobah E, Koenen KC, Kariuki S, Zingela Z, Akena D, Newton C, Atwoli L, Teferra S, Stein DJ, Gelaye B. Cross-country variations in the reporting of psychotic symptoms among sub-Saharan African adults: A psychometric evaluation of the Psychosis Screening Questionnaire. J Affect Disord. 2022 May 1;304:85-92. doi: 10.1016/j.jad.2022.02.048. Epub 2022 Feb 18. PubMed PMID: 35183621; PubMed Central PMCID: PMC9036658.

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Mars N, Kerminen S, Feng YA, Kanai M, Läll K, Thomas LF, Skogholt AH, Della Briotta Parolo P, Neale BM, Smoller JW, Gabrielsen ME, Hveem K, Mägi R, Matsuda K, Okada Y, Pirinen M, Palotie A, Ganna A, Martin AR, Ripatti S. Genome-wide risk prediction of common diseases across ancestries in one million people. Cell Genom. 2022 Apr 13;2(4):None. doi: 10.1016/j.xgen.2022.100118. PubMed PMID: 35591975; PubMed Central PMCID: PMC9010308.