Nature Search

Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Genome-wide association meta-analyses of attention-deficit/hyperactivity disorder symptom measures and clinical diagnoses identify new risk loci, highlight putative effector genes and yield improved polygenic risk scores.

Camiel M. van der Laan
Hill F. Ip
Dorret I. Boomsma
Research17 Sept 2025
Nature Genetics

Volume: 57, P: 2427-2435
The Earliest Published Figures (1613–1758) of the Oblong or Truncate-tailed Ocean Sunfish, Ranzania truncata

E. W. GUDGER
Research01 Jun 1936
Nature

Volume: 137, P: 947-948
Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Camiel M. van der Laan
Hill F. Ip
Dorret I. Boomsma
Amendments and Corrections29 Sept 2025
Nature Genetics

Volume: 57, P: 2604
Methylation status of p14ARF and p16INK4a as detected in pancreatic secretions

B Klump
C J Hsieh
M Gregor
ResearchOpen Access28 Jan 2003
British Journal of Cancer

Volume: 88, P: 217-222
Studies on p53, BAX and Bcl-2 protein expression and microsatellite instability in stage III (UICC) colon cancer treated by adjuvant chemotherapy: major prognostic impact of proapoptotic BAX

O Nehls
T Okech
B Klump
ResearchOpen Access10 Apr 2007
British Journal of Cancer

Volume: 96, P: 1409-1418
A landscape of response to drug combinations in non-small cell lung cancer

Combination of drugs within cancer treatment is a popular way to overcome resistance and increase efficacy. Here, the authors analyse over 5000 targeted agent combinations in non-small cell lung cancer to identify potentially effective drug strategies.

Nishanth Ulhas Nair
Patricia Greninger
Cyril H. Benes
ResearchOpen Access28 Jun 2023
Nature Communications

Volume: 14, P: 1-19
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

Integration of GWAS and single-cell transcriptomic data from the entire nervous system systematically identifies cell types underlying brain complex traits and provides insights into the etiology of Parkinson’s disease.

Julien Bryois
Nathan G. Skene
Patrick F. Sullivan
Research27 Apr 2020
Nature Genetics

Volume: 52, P: 482-493
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Genome-wide analyses identify eight independent loci associated with anorexia nervosa. Genetic correlations implicate both psychiatric and metabolic components in the etiology of this disorder, even after adjusting for the effects of common variants associated with body mass index.

Hunna J. Watson
Zeynep Yilmaz
Cynthia M. Bulik
Research15 Jul 2019
Nature Genetics

Volume: 51, P: 1207-1214
KRAS mutation detection and prognostic potential in sporadic colorectal cancer using high-resolution melting analysis

V Deschoolmeester
C Boeckx
J B Vermorken
ResearchOpen Access19 Oct 2010
British Journal of Cancer

Volume: 103, P: 1627-1636
Oxaliplatin, fluorouracil and leucovorin for advanced biliary system adenocarcinomas: a prospective phase II trial

O Nehls
B Klump
R Porschen
ResearchOpen Access23 Sept 2002
British Journal of Cancer

Volume: 87, P: 702-704
Leveraging transdiagnostic genetic liability to psychiatric disorders to dissect clinical outcomes of anorexia nervosa

Zheng-An Lu
Alexander Ploner
Sarah E. Bergen
ResearchOpen Access23 Sept 2025
Molecular Psychiatry

P: 1-10
Discovery of species-wide tool use in the Hawaiian crow

A species-wide study shows that the Hawaiian crow Corvus hawaiiensis is a highly proficient tool user, creating opportunities for comparative studies with tool-using New Caledonian crows and other corvids.

Christian Rutz
Barbara C. Klump
Bryce M. Masuda
Research14 Sept 2016
Nature

Volume: 537, P: 403-407
ANIMAL-SPOT enables animal-independent signal detection and classification using deep learning

Christian Bergler
Simeon Q. Smeele
Barbara C. Klump
ResearchOpen Access19 Dec 2022
Scientific Reports

Volume: 12, P: 1-16
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

Exome sequencing identifies mutations in kelch-like 3 and cullin 3 as causes of a syndrome featuring high blood pressure and electrolyte abnormalities.

Lynn M. Boyden
Murim Choi
Richard P. Lifton
Research22 Jan 2012
Nature

Volume: 482, P: 98-102
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

A Hinney
M Kesselmeier
J Hebebrand
Research17 May 2016
Molecular Psychiatry

Volume: 22, P: 192-201
The MHC and non-random mating in a captive population of Chinook salmon

B D Neff
S R Garner
D D Heath
Research28 May 2008
Heredity

Volume: 101, P: 175-185
Retroviral vector-mediated expression of HoxB4 in hematopoietic cells using a novel coexpression strategy

H Klump
B Schiedlmeier
C Baum
Research22 Jun 2001
Gene Therapy

Volume: 8, P: 811-817
Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts

Aline Jelenkovic
Reijo Sund
Karri Silventoinen
ResearchOpen Access19 Apr 2018
Scientific Reports

Volume: 8, P: 1-8
Genetic association study of childhood aggression across raters, instruments, and age

Hill F. Ip
Camiel M. van der Laan
Dorret I. Boomsma
ResearchOpen Access30 Jul 2021
Translational Psychiatry

Volume: 11, P: 1-9
Association of Multiple DRD2 Polymorphisms with Anorexia Nervosa

Andrew W Bergen
Meredith Yeager
Walter H Kaye
Research25 May 2005
Neuropsychopharmacology

Volume: 30, P: 1703-1710
Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

Karri Silventoinen
Weilong Li
Jaakko Kaprio
ResearchOpen Access09 Aug 2022
International Journal of Obesity

Volume: 46, P: 1901-1909
Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts

Aline Jelenkovic
Reijo Sund
Karri Silventoinen
ResearchOpen Access23 Jun 2016
Scientific Reports

Volume: 6, P: 1-13
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Dong Li
Xiao Chang
Hakon Hakonarson
ResearchOpen Access19 Jun 2017
Scientific Reports

Volume: 7, P: 1-8
Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education

Aline Jelenkovic
Reijo Sund
Karri Silventoinen
ResearchOpen Access14 May 2020
Scientific Reports

Volume: 10, P: 1-11
Using ancestry-informative markers to identify fine structure across 15 populations of European origin

Laura M Huckins
Vesna Boraska
Ioanna Tachmazidou
ResearchOpen Access19 Feb 2014
European Journal of Human Genetics

Volume: 22, P: 1190-1200
Extremozymes: Expanding the Limits of Biocatalysis

Michael W.W. Adams
Francine B. Perler
Robert M. Kelly
Reviews01 Jul 1995
Bio/Technology

Volume: 13, P: 662-668
Defining suicidality phenotypes for genetic studies: perspectives of the Psychiatric Genomics Consortium Suicide Working Group

Sarah M. C. Colbert
Eric T. Monson
Lea Zillich
ReviewsOpen Access25 Sept 2025
Molecular Psychiatry

Volume: 30, P: 6144-6154
A genome-wide association study of anorexia nervosa

V Boraska
C S Franklin
C M Bulik
Research11 Feb 2014
Molecular Psychiatry

Volume: 19, P: 1085-1094
Genetic Association of Recovery from Eating Disorders: The Role of GABA Receptor SNPs

Cinnamon S Bloss
Wade Berrettini
Walter H Kaye
Research13 Jul 2011
Neuropsychopharmacology

Volume: 36, P: 2222-2232
Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder

Zeynep Yilmaz
Matthew Halvorsen
James J. Crowley
Research07 Aug 2018
Molecular Psychiatry

Volume: 25, P: 2036-2046
Capecitabine plus oxaliplatin as first-line treatment in patients with advanced biliary system adenocarcinoma: a prospective multicentre phase II trial

O Nehls
H Oettle
B Klump
ResearchOpen Access08 Jan 2008
British Journal of Cancer

Volume: 98, P: 309-315
Self-inactivating retroviral vectors with improved RNA processing

J Kraunus
DHS Schaumann
C Baum
Research16 Sept 2004
Gene Therapy

Volume: 11, P: 1568-1578
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

L M Huckins
K Hatzikotoulas
E Zeggini
ResearchOpen Access25 Jul 2017
Molecular Psychiatry

Volume: 23, P: 1169-1180
Evidence for the role of EP HX2 gene variants in anorexia nervosa

A A Scott-Van Zeeland
C S Bloss
N J Schork
ResearchOpen Access03 Sept 2013
Molecular Psychiatry

Volume: 19, P: 724-732
Candidate genes for anorexia nervosa in the 1p33–36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa

A W Bergen
M B M van den Bree
W H Kaye
Research09 May 2003
Molecular Psychiatry

Volume: 8, P: 397-406
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Dong Li
Xiao Chang
Hakon Hakonarson
Amendments and CorrectionsOpen Access21 Aug 2017
Scientific Reports

Volume: 7, P: 1-4
A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

K Wang
H Zhang
H Hakonarson
Research16 Nov 2010
Molecular Psychiatry

Volume: 16, P: 949-959

Search

Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

The Earliest Published Figures (1613–1758) of the Oblong or Truncate-tailed Ocean Sunfish, Ranzania truncata

Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes

Methylation status of p14ARF and p16INK4a as detected in pancreatic secretions

Studies on p53, BAX and Bcl-2 protein expression and microsatellite instability in stage III (UICC) colon cancer treated by adjuvant chemotherapy: major prognostic impact of proapoptotic BAX

A landscape of response to drug combinations in non-small cell lung cancer

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

KRAS mutation detection and prognostic potential in sporadic colorectal cancer using high-resolution melting analysis

Oxaliplatin, fluorouracil and leucovorin for advanced biliary system adenocarcinomas: a prospective phase II trial

Leveraging transdiagnostic genetic liability to psychiatric disorders to dissect clinical outcomes of anorexia nervosa

Discovery of species-wide tool use in the Hawaiian crow

ANIMAL-SPOT enables animal-independent signal detection and classification using deep learning

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

The MHC and non-random mating in a captive population of Chinook salmon

Retroviral vector-mediated expression of HoxB4 in hematopoietic cells using a novel coexpression strategy

Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts

Genetic association study of childhood aggression across raters, instruments, and age

Association of Multiple DRD2 Polymorphisms with Anorexia Nervosa

Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

Genetic and environmental influences on height from infancy to early adulthood: An individual-based pooled analysis of 45 twin cohorts

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education

Using ancestry-informative markers to identify fine structure across 15 populations of European origin

Extremozymes: Expanding the Limits of Biocatalysis

Defining suicidality phenotypes for genetic studies: perspectives of the Psychiatric Genomics Consortium Suicide Working Group

A genome-wide association study of anorexia nervosa

Genetic Association of Recovery from Eating Disorders: The Role of GABA Receptor SNPs

Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder

Capecitabine plus oxaliplatin as first-line treatment in patients with advanced biliary system adenocarcinoma: a prospective multicentre phase II trial

Self-inactivating retroviral vectors with improved RNA processing

Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

Evidence for the role of EP HX2 gene variants in anorexia nervosa

Candidate genes for anorexia nervosa in the 1p33–36 linkage region: serotonin 1D and delta opioid receptor loci exhibit significant association to anorexia nervosa

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa

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