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Ajay Prabhakar Nadig

TitleProf,Asst
InstitutionUniversity of Oklahoma Health Sciences Center
DepartmentGeneral Internal Medicine
AddressAAT 6300
800 Stanton L Young Blvd
Oklahoma City OK 73104
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Schaffer L, Rau S, Larsen IG, Clasen L, Warling A, Whitman ET, Nadig A, McDermott C, Xenophontos A, Wilson K, Blumenthal J, Torres E, Raznahan A. X- vs. Y-chromosome influences on human behavior: a deep phenotypic comparison of psychopathology in XXY and XYY syndromes. J Neurodev Disord. 2024 Oct 03; 16(1):56. PMID: 39363182; PMCID: PMC11451104.
      Citations:    Fields:    Translation:HumansCells
    2. Adebekun J, Nadig A, Saarah P, Asgari S, Kachuri L, Alagpulinsa DA. Genetic relations between type 1 diabetes, coronary artery disease and leukocyte counts. Diabetologia. 2024 Aug 14. PMID: 39141130.
      Citations:    Fields:    
    3. Nadig A, Replogle JM, Pogson AN, McCarroll SA, Weissman JS, Robinson EB, O'Connor LJ. Transcriptome-wide characterization of genetic perturbations. bioRxiv. 2024 Jul 03. PMID: 39005298; PMCID: PMC11244993.
      Citations:    
    4. Tegtmeyer M, Arora J, Asgari S, Cimini BA, Nadig A, Peirent E, Liyanage D, Way GP, Weisbart E, Nathan A, Amariuta T, Eggan K, Haghighi M, McCarroll SA, O'Connor L, Carpenter AE, Singh S, Nehme R, Raychaudhuri S. High-dimensional phenotyping to define the genetic basis of cellular morphology. Nat Commun. 2024 Jan 06; 15(1):347. PMID: 38184653; PMCID: PMC10771466.
      Citations: 4     Fields:    Translation:Cells
    5. Rodin RE, Dou Y, Kwon M, Sherman MA, D'Gama AM, Doan RN, Rento LM, Girskis KM, Bohrson CL, Kim SN, Nadig A, Luquette LJ, Gulhan DC, Brain Somatic Mosaicism Network, Park PJ, Walsh CA. Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2023 Oct; 26(10):1833. PMID: 37644260.
      Citations:    Fields:    
    6. Schaffer L, Rau S, Clasen L, Warling A, Whitman ET, Nadig A, McDermott C, Xenophontos A, Wilson K, Blumenthal J, Torres E, Raznahan A. X- vs. Y-Chromosome Influences on Human Behavior: A Deep Phenotypic Comparison of Psychopathology in XXY and XYY Syndromes. medRxiv. 2023 Jun 27. PMID: 37502878; PMCID: PMC10371113.
      Citations:    
    7. Glover J, Nadig A, Vesely S, Neelakantan D, Williams KM, Holter-Chakrabarty J. Fluorothymidine PET/CT Identifies a Case of Herpes Simplex Virus Esophagitis. Radiol Imaging Cancer. 2023 03; 5(2):e220141. PMID: 36961315; PMCID: PMC10077096.
      Citations:    Fields:    Translation:HumansCells
    8. Weiner DJ, Nadig A, Jagadeesh KA, Dey KK, Neale BM, Robinson EB, Karczewski KJ, O'Connor LJ. Polygenic architecture of rare coding variation across 394,783 exomes. Nature. 2023 Feb; 614(7948):492-499. PMID: 36755099.
      Citations: 33     Fields:    Translation:Humans
    9. Gupta T, Osborne KJ, Nadig A, Haase CM, Mittal VA. Alterations in facial expressions in individuals at risk for psychosis: a facial electromyography approach using emotionally evocative film clips. Psychol Med. 2022 Oct 26; 1-10. PMID: 36285533; PMCID: PMC10130238.
      Citations: 3     Fields:    Translation:Humans
    10. Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Carey CE, Baya N, Bybjerg-Grauholm J, iPSYCH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta S, Macosko EZ, Sebat J, O'Connor LJ, Hougaard DM, B?rglum AD, Talkowski ME, McCarroll SA, Robinson EB. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nat Genet. 2022 11; 54(11):1630-1639. PMID: 36280734; PMCID: PMC9649437.
      Citations: 9     Fields:    Translation:HumansCells
    11. Whitman ET, Liu S, Torres E, Warling A, Wilson K, Nadig A, McDermott C, Clasen LS, Blumenthal JD, Lalonde FM, Gotts SJ, Martin A, Raznahan A. Resting-State Functional Connectivity and Psychopathology in Klinefelter Syndrome (47, XXY). Cereb Cortex. 2021 07 29; 31(9):4180-4190. PMID: 34009243.
      Citations: 3     Fields:    Translation:HumansCells
    12. Warling A, McDermott CL, Liu S, Seidlitz J, Rodrigue AL, Nadig A, Gur RC, Gur RE, Roalf D, Moore TM, Glahn D, Satterthwaite TD, Bullmore ET, Raznahan A. Regional White Matter Scaling in the Human Brain. J Neurosci. 2021 08 18; 41(33):7015-7028. PMID: 34244364.
      Citations: 4     Fields:    Translation:Humans
    13. Nadig A, Seidlitz J, McDermott CL, Liu S, Bethlehem R, Moore TM, Mallard TT, Clasen LS, Blumenthal JD, Lalonde F, Gur RC, Gur RE, Bullmore ET, Satterthwaite TD, Raznahan A. Morphological integration of the human brain across adolescence and adulthood. Proc Natl Acad Sci U S A. 2021 04 06; 118(14). PMID: 33811142.
      Citations: 12     Fields:    Translation:Humans
    14. Rodin RE, Dou Y, Kwon M, Sherman MA, D'Gama AM, Doan RN, Rento LM, Girskis KM, Bohrson CL, Kim SN, Nadig A, Luquette LJ, Gulhan DC, Park PJ, Walsh CA. Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 Apr; 24(4):611. PMID: 33753946.
      Citations: 4     Fields:    
    15. Rodin RE, Dou Y, Kwon M, Sherman MA, D'Gama AM, Doan RN, Rento LM, Girskis KM, Bohrson CL, Kim SN, Nadig A, Luquette LJ, Gulhan DC, Park PJ, Walsh CA. The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 02; 24(2):176-185. PMID: 33432195.
      Citations: 57     Fields:    Translation:HumansCells
    16. Seidlitz J, Nadig A, Liu S, Bethlehem RAI, Vértes PE, Morgan SE, Váša F, Romero-Garcia R, Lalonde FM, Clasen LS, Blumenthal JD, Paquola C, Bernhardt B, Wagstyl K, Polioudakis D, de la Torre-Ubieta L, Geschwind DH, Han JC, Lee NR, Murphy DG, Bullmore ET, Raznahan A. Author Correction: Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders. Nat Commun. 2020 Nov 17; 11(1):5936. PMID: 33203864.
      Citations: 3     Fields:    
    17. Seidlitz J, Nadig A, Liu S, Bethlehem RAI, Vértes PE, Morgan SE, Váša F, Romero-Garcia R, Lalonde FM, Clasen LS, Blumenthal JD, Paquola C, Bernhardt B, Wagstyl K, Polioudakis D, de la Torre-Ubieta L, Geschwind DH, Han JC, Lee NR, Murphy DG, Bullmore ET, Raznahan A. Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders. Nat Commun. 2020 07 03; 11(1):3358. PMID: 32620757.
      Citations: 91     Fields:    Translation:HumansCells
    18. Fish AM, Nadig A, Seidlitz J, Reardon PK, Mankiw C, McDermott CL, Blumenthal JD, Clasen LS, Lalonde F, Lerch JP, Chakravarty MM, Shinohara RT, Raznahan A. Sex-biased trajectories of amygdalo-hippocampal morphology change over human development. Neuroimage. 2020 01 01; 204:116122. PMID: 31470127.
      Citations: 14     Fields:    Translation:Humans
    19. Nadig A, Kelley NJ, Pornpattananangkul N, Glazer JE, Nusslock R. Shifts in attentional scope modulate event-related potentials evoked by reward. Cogn Affect Behav Neurosci. 2019 06; 19(3):586-599. PMID: 30859386.
      Citations: 2     Fields:    Translation:Humans
    20. McDermott CL, Seidlitz J, Nadig A, Liu S, Clasen LS, Blumenthal JD, Reardon PK, Lalonde F, Greenstein D, Patel R, Chakravarty MM, Lerch JP, Raznahan A. Longitudinally Mapping Childhood Socioeconomic Status Associations with Cortical and Subcortical Morphology. J Neurosci. 2019 02 20; 39(8):1365-1373. PMID: 30587541.
      Citations: 75     Fields:    Translation:Humans
    21. Nadig A, Reardon PK, Seidlitz J, McDermott CL, Blumenthal JD, Clasen LS, Lalonde F, Lerch JP, Chakravarty MM, Raznahan A. Carriage of Supernumerary Sex Chromosomes Decreases the Volume and Alters the Shape of Limbic Structures. eNeuro. 2018 Sep-Oct; 5(5). PMID: 30713992.
      Citations: 13     Fields:    Translation:HumansCells
    22. Aicher TP, Barabási DL, Harris BD, Nadig A, Williams KL. Ten simple rules for getting the most out of a summer laboratory internship. PLoS Comput Biol. 2017 Aug; 13(8):e1005606. PMID: 28817622.
      Citations: 5     Fields:    
    23. Pornpattananangkul N, Nadig A, Heidinger S, Walden K, Nusslock R. Elevated outcome-anticipation and outcome-evaluation ERPs associated with a greater preference for larger-but-delayed rewards. Cogn Affect Behav Neurosci. 2017 06; 17(3):625-641. PMID: 28224457.
      Citations: 10     Fields:    Translation:Humans
    24. Sawalha AH, Wang L, Nadig A, Somers EC, McCune WJ, Hughes T, Merrill JT, Scofield RH, Strickland FM, Richardson B. Sex-specific differences in the relationship between genetic susceptibility, T cell DNA demethylation and lupus flare severity. J Autoimmun. 2012 May; 38(2-3):J216-22. PMID: 22305513.
      Citations: 29     Fields:    Translation:HumansCells
    25. Sawalha AH, Hughes T, Nadig A, Yilmaz V, Aksu K, Keser G, Cefle A, Yazici A, Ergen A, Alarcón-Riquelme ME, Salvarani C, Casali B, Direskeneli H, Saruhan-Direskeneli G. A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease. Arthritis Rheum. 2011 Nov; 63(11):3607-12. PMID: 21918955.
      Citations: 21     Fields:    Translation:Humans
    26. Sanchez E, Nadig A, Richardson BC, Freedman BI, Kaufman KM, Kelly JA, Niewold TB, Kamen DL, Gilkeson GS, Ziegler JT, Langefeld CD, Alarcón GS, Edberg JC, Ramsey-Goldman R, Petri M, Brown EE, Kimberly RP, Reveille JD, Vilá LM, Merrill JT, Anaya JM, James JA, Pons-Estel BA, Martin J, Park SY, Bang SY, Bae SC, Moser KL, Vyse TJ, Criswell LA, Gaffney PM, Tsao BP, Jacob CO, Harley JB, Alarcón-Riquelme ME, Sawalha AH. Phenotypic associations of genetic susceptibility loci in systemic lupus erythematosus. Ann Rheum Dis. 2011 Oct; 70(10):1752-7. PMID: 21719445.
      Citations: 68     Fields:    Translation:Humans
    27. Htoon J, Nadig A, Hughes T, Yavuz S, Direskeneli H, Saruhan-Direskeneli G, Sawalha AH. IL18 polymorphism is associated with Behçet's disease but not lupus in patients from Turkey. J Rheumatol. 2011 May; 38(5):962-3. PMID: 21532063.
      Citations: 5     Fields:    Translation:Humans
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