Citation Impact
Citing Papers
Chromosome Abnormalities and Genetic Counseling
2011
Beyond the fourth wave of genome-wide obesity association studies
2012
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
An integrated map of genetic variation from 1,092 human genomes
2012 StandoutNature
Chipping Away the ‘Missing Heritability’: GIANT Steps Forward in the Molecular Elucidation of Obesity – but Still Lots to Go
2010
Benefits and limitations of genome-wide association studies
2019
A guide to genome engineering with programmable nucleases
2014 Standout
Oxyl radicals, redox-sensitive signalling cascades and antioxidants
2007 Standout
Large multiallelic copy number variations in humans
2015
The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans
2002 StandoutNobel
Novel droplet platforms for the detection of disease biomarkers
2014
The scent of disease: volatile organic compounds of the human body related to disease and disorder
2011 Standout
Targeted chromosomal duplications and inversions in the human genome using zinc finger nucleases
2011
Rare and Common Genetic Events in Type 2 Diabetes: What Should Biologists Know?
2015
Investigation of Mendelian forms of obesity holds out the prospect of personalized medicine
2010
Fibrosis and Adipose Tissue Dysfunction
2013 Standout
Clinical practice guidelines for the perioperative nutritional, metabolic, and nonsurgical support of the bariatric surgery patient—2013 update: Cosponsored by american association of clinical endocrinologists, The obesity society, and american society for metabolic & bariatric surgery*
2013 Standout
The ground state of embryonic stem cell self-renewal
2008 StandoutNature
ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering
2013 Standout
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism
2016 StandoutNobel
REPuter: the manifold applications of repeat analysis on a genomic scale
2001 Standout
Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond
2014
Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes
2012
Mendelian randomization: genetic anchors for causal inference in epidemiological studies
2014 Standout
Clan Genomics and the Complex Architecture of Human Disease
2011
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia
2011
Reactive oxygen species (ROS) as pleiotropic physiological signalling agents
2020 Standout
A role of PIEZO1 in iron metabolism in mice and humans
2021 StandoutNobel
Management of Malignant Fungating Wounds in Advanced Cancer
2006
Biochemical and cellular properties of insulin receptor signalling
2017
Type 2 diabetes
2017 Standout
Genetic architecture in autism spectrum disorder
2012
Autism
2013 Standout
The conundrums of understanding genetic risks for autism spectrum disorders
2011
Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies
2010
Genomic Copy Number Variation in Disorders of Cognitive Development
2010
Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study
2013 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
22q11.2 deletion syndrome
2015 Standout
Genetics and epigenetics in obesity
2018
Gut microbiota in human metabolic health and disease
2020 Standout
Identification of copy number variants in whole-genome data using Reference Coverage Profiles
2015 StandoutNobel
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
The Fibroblast Growth Factor signaling pathway
2015 Standout
Improving detection of copy-number variation by simultaneous bias correction and read-depth segmentation
2012
Mechanisms of Insulin Action and Insulin Resistance
2018 Standout
Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion
2011
Sex and Gender Differences in Risk, Pathophysiology and Complications of Type 2 Diabetes Mellitus
2016 Standout
Genetic Syndromes of Severe Insulin Resistance
2011
AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome
2002 StandoutNobel
Pathophysiology of Type 2 Diabetes Mellitus
2020 Standout
Recent Findings on the Genetics of Obesity: Is there Public Health Relevance?
2012
Conditional Deletion of Focal Adhesion Kinase Leads to Defects in Ventricular Septation and Outflow Tract Alignment
2007 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Insulin Resistance and the Polycystic Ovary Syndrome Revisited: An Update on Mechanisms and Implications
2012 Standout
Regulation of insulin and type 1 insulin‐like growth factor signaling and action by the G rb10/14 and SH 2B 1/B 2 adaptor proteins
2012
Childhood Obesity
2012
Obesity: global epidemiology and pathogenesis
2019 Standout
Emerging Droplet Microfluidics
2017 Standout
Works of Sadia Saeed being referenced
High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families
2012
Cutaneous metastasis: a clinical, pathological, and immunohistochemical appraisal
2004
Large, rare chromosomal deletions associated with severe early-onset obesity
2009 Nature
Genetics of Obesity in Consanguineous Populations: Toward Precision Medicine and the Discovery of Novel Obesity Genes
2018
Highly Sensitive Diagnosis of 43 Monogenic Forms of Diabetes or Obesity Through One-Step PCR-Based Enrichment in Combination With Next-Generation Sequencing
2013