SwePub
Tyck till om SwePub Sök här!
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "LAR1:ki ;pers:(Lichtenstein P)"

Sökning: LAR1:ki > Lichtenstein P

  • Resultat 1-10 av 648
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Ahlberg, Rickard, 1970-, et al. (författare)
  • Real-life instability in ADHD from young to middle adulthood : a nationwide register-based study of social and occupational problems
  • 2023
  • Ingår i: BMC Psychiatry. - : BioMed Central (BMC). - 1471-244X. ; 23:1
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Studies using self-reports indicate that individuals with ADHD are at increased risk for functional impairments in social and occupational settings, but evidence around real-life instability remains limited. It is furthermore unclear if these functional impairments in ADHD differ across sex and across the adult lifespan.METHOD: A longitudinal observational cohort design of 3,448,440 individuals was used to study the associations between ADHD and residential moves, relational instability and job shifting using data from Swedish national registers. Data were stratified on sex and age (18-29 years, 30-39 years, and 40-52 years at start of follow up).RESULTS: 31,081 individuals (17,088 males; 13,993 females) in the total cohort had an ADHD-diagnosis. Individuals with ADHD had an increased incidence rate ratio (IRR) of residential moves (IRR 2.35 [95% CI, 2.32-2.37]), relational instability (IRR = 1.07 [95% CI, 1.06-1.08]) and job shifting (IRR = 1.03 [95% CI, 1.02-1.04]). These associations tended to increase with increasing age. The strongest associations were found in the oldest group (40-52 years at start of follow). Women with ADHD in all three age groups had a higher rate of relational instability compared to men with ADHD.CONCLUSION: Both men and women with a diagnosis of ADHD present with an increased risk of real-life instability in different domains and this behavioral pattern was not limited to young adulthood but also existed well into older adulthood. It is therefore important to have a lifespan perspective on ADHD for individuals, relatives, and the health care sector.
  •  
2.
  •  
3.
  •  
4.
  • Akingbuwa, W. A., et al. (författare)
  • Genetic Associations between Childhood Psychopathology and Adult Depression and Associated Traits in 42998 Individuals: A Meta-Analysis
  • 2020
  • Ingår i: JAMA Psychiatry. - : American Medical Association (AMA). - 2168-622X .- 2168-6238. ; 77:7, s. 715-728
  • Tidskriftsartikel (refereegranskat)abstract
    • Importance: Adult mood disorders are often preceded by behavioral and emotional problems in childhood. It is yet unclear what explains the associations between childhood psychopathology and adult traits. Objective: To investigate whether genetic risk for adult mood disorders and associated traits is associated with childhood disorders. Design, Setting, and Participants: This meta-analysis examined data from 7 ongoing longitudinal birth and childhood cohorts from the UK, the Netherlands, Sweden, Norway, and Finland. Starting points of data collection ranged from July 1985 to April 2002. Participants were repeatedly assessed for childhood psychopathology from ages 6 to 17 years. Data analysis occurred from September 2017 to May 2019. Exposures: Individual polygenic scores (PGS) were constructed in children based on genome-wide association studies of adult major depression, bipolar disorder, subjective well-being, neuroticism, insomnia, educational attainment, and body mass index (BMI). Main Outcomes and Measures: Regression meta-analyses were used to test associations between PGS and attention-deficit/hyperactivity disorder (ADHD) symptoms and internalizing and social problems measured repeatedly across childhood and adolescence and whether these associations depended on childhood phenotype, age, and rater. Results: The sample included 42998 participants aged 6 to 17 years. Male participants varied from 43.0% (1040 of 2417 participants) to 53.1% (2434 of 4583 participants) by age and across all cohorts. The PGS of adult major depression, neuroticism, BMI, and insomnia were positively associated with childhood psychopathology (β estimate range, 0.023-0.042 [95% CI, 0.017-0.049]), while associations with PGS of subjective well-being and educational attainment were negative (β, -0.026 to -0.046 [95% CI, -0.020 to -0.057]). There was no moderation of age, type of childhood phenotype, or rater with the associations. The exceptions were stronger associations between educational attainment PGS and ADHD compared with internalizing problems (Δβ, 0.0561 [Δ95% CI, 0.0318-0.0804]; ΔSE, 0.0124) and social problems (Δβ, 0.0528 [Δ95% CI, 0.0282-0.0775]; ΔSE, 0.0126), and between BMI PGS and ADHD and social problems (Δβ, -0.0001 [Δ95% CI, -0.0102 to 0.0100]; ΔSE, 0.0052), compared with internalizing problems (Δβ, -0.0310 [Δ95% CI, -0.0456 to -0.0164]; ΔSE, 0.0074). Furthermore, the association between educational attainment PGS and ADHD increased with age (Δβ, -0.0032 [Δ 95% CI, -0.0048 to -0.0017]; ΔSE, 0.0008). Conclusions and Relevance: Results from this study suggest the existence of a set of genetic factors influencing a range of traits across the life span with stable associations present throughout childhood. Knowledge of underlying mechanisms may affect treatment and long-term outcomes of individuals with psychopathology.. © 2020 Lippincott Williams and Wilkins. All rights reserved.
  •  
5.
  • Akingbuwa, W. A., et al. (författare)
  • Multivariate analyses of molecular genetic associations between childhood psychopathology and adult mood disorders and related traits
  • 2022
  • Ingår i: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics. - : Wiley. - 1552-4841 .- 1552-485X. ; 192:1-2, s. 3-12
  • Tidskriftsartikel (refereegranskat)abstract
    • Ubiquitous associations have been detected between different types of childhood psychopathology and polygenic risk scores based on adult psychiatric disorders and related adult outcomes, indicating that genetic factors partly explain the association between childhood psychopathology and adult outcomes. However, these analyses in general do not take into account the correlations between the adult trait and disorder polygenic risk scores. This study aimed to further clarify the influence of genetic factors on associations between childhood psychopathology and adult outcomes by accounting for these correlations. Using a multivariate multivariable regression, we analyzed associations of childhood attention-deficit/hyperactivity disorder (ADHD), internalizing, and social problems, with polygenic scores (PGS) of adult disorders and traits including major depression, bipolar disorder, subjective well-being, neuroticism, insomnia, educational attainment, and body mass index (BMI), derived for 20,539 children aged 8.5-10.5 years. After correcting for correlations between the adult phenotypes, major depression PGS were associated with all three childhood traits, that is, ADHD, internalizing, and social problems. In addition, BMI PGS were associated with ADHD symptoms and social problems, while neuroticism PGS were only associated with internalizing problems and educational attainment PGS were only associated with ADHD symptoms. PGS of bipolar disorder, subjective well-being, and insomnia were not associated with any childhood traits. Our findings suggest that associations between childhood psychopathology and adult traits like insomnia and subjective well-being may be primarily driven by genetic factors that influence adult major depression. Additionally, specific childhood phenotypes are genetically associated with educational attainment, BMI and neuroticism.
  •  
6.
  •  
7.
  • Alexanderson, Camilla, 1978, et al. (författare)
  • Influence of having a male twin on body mass index and risk for dyslipidemia in middle-aged and old women.
  • 2011
  • Ingår i: International Journal of Obesity. - : Springer Science and Business Media LLC. - 0307-0565 .- 1476-5497. ; 35
  • Tidskriftsartikel (refereegranskat)abstract
    • Background:Animal experiments suggest that exposure to elevated levels of androgens during development by means of so-called hormonal programming causes metabolic aberrations at adulthood. An indirect strategy to address the possible importance of such an influence also in humans would be to study female dizygotic twins, presuming that those with a twin brother-due to diffusion of testosterone-have been exposed to higher androgen levels prenatally.Design:We have compared 8409 women with a male twin with 9166 women with a dizygotic female twin with respect to self-reported indices of anthropometry and metabolic aberrations at age 42 or older.Results:Body mass index (BMI), body weight and rate of dyslipidemia were moderately, but significantly, higher in women from opposite-sexed (OS) twin pairs; splitting for age revealed this difference to be present in those 60 years of age only.Conclusion:The results (i) support the notion that comparisons of women with a twin brother with women from same-sexed twin pairs may be used to shed light on possible long-term effects of interindividual variations in early androgen exposure, and (ii) suggest that the effects of early androgen exposure on metabolism previously observed in animal experiments are of relevance also for humans.International Journal of Obesity advance online publication, 8 March 2011; doi:10.1038/ijo.2011.18.
  •  
8.
  • Algars, M, et al. (författare)
  • Binge eating and menstrual dysfunction
  • 2014
  • Ingår i: Journal of psychosomatic research. - : Elsevier BV. - 1879-1360 .- 0022-3999. ; 76:1, s. 19-22
  • Tidskriftsartikel (refereegranskat)
  •  
9.
  • Algovik, M, et al. (författare)
  • Genetic influence on dystocia
  • 2004
  • Ingår i: Acta obstetricia et gynecologica Scandinavica. - : Wiley. - 0001-6349. ; 83:9, s. 832-837
  • Tidskriftsartikel (refereegranskat)
  •  
10.
  • Algovik, M, et al. (författare)
  • Genetic influence on dystocia
  • 2003
  • Ingår i: AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY. - : Elsevier BV. - 0002-9378. ; 189:6, s. S113-S113
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 648
Typ av publikation
tidskriftsartikel (430)
konferensbidrag (216)
forskningsöversikt (2)
Typ av innehåll
refereegranskat (400)
övrigt vetenskapligt/konstnärligt (248)
Författare/redaktör
Lichtenstein, P. (648)
Larsson, H (103)
Kuja-Halkola, R. (83)
Langstrom, N (75)
Larsson, Henrik, 197 ... (60)
Pedersen, NL (52)
visa fler...
Lundström, Sebastian (48)
Reiss, D (44)
D'Onofrio, B (43)
Cnattingius, S (39)
Fazel, S (38)
Almqvist, C (37)
Neiderhiser, JM (37)
D'Onofrio, BM (36)
Landen, M (35)
Lundstrom, S (35)
Kaprio, J (30)
Bulik, CM (30)
Hultman, CM (30)
Bartels, M (29)
Spotts, EL (29)
Sullivan, PF (28)
Mataix-Cols, D (28)
Pettersson, E (28)
Landén, Mikael, 1966 (26)
Kendler, KS (25)
Chang, Z (22)
Martin, J. (21)
Thornton, LM (21)
Plomin, R (20)
Runeson, B. (20)
Magnusson, PKE (19)
Boomsma, DI (18)
Breen, G (18)
Ruck, C (18)
Cichon, S (18)
Martin, NG (18)
Ganiban, J (18)
Sandin, S (18)
Ganiban, JM (18)
Tiemeier, H (17)
Ripke, S (17)
Brikell, I (17)
Sariaslan, A. (17)
Rujescu, D (16)
Sklar, P (16)
Anckarsäter, Henrik, ... (16)
Butwicka, A (16)
Giegling, I (16)
Hellner, C (16)
visa färre...
Lärosäte
Karolinska Institutet (648)
Göteborgs universitet (98)
Örebro universitet (71)
Uppsala universitet (16)
Lunds universitet (11)
Jönköping University (6)
visa fler...
Handelshögskolan i Stockholm (5)
Umeå universitet (3)
Högskolan Väst (3)
Högskolan i Skövde (3)
Gymnastik- och idrottshögskolan (3)
Högskolan i Halmstad (2)
Kungliga Tekniska Högskolan (1)
Högskolan i Gävle (1)
Mälardalens universitet (1)
Linköpings universitet (1)
visa färre...
Språk
Engelska (648)
Forskningsämne (UKÄ/SCB)
Medicin och hälsovetenskap (144)
Samhällsvetenskap (32)
Naturvetenskap (12)

År

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy