صدف فاروقي طبيبة استشارية بريطانية
Farooqi, I. Sadaf
Farooqi, I. Sadaf, 19..-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
فاروقي، صدف
VIAF ID: 56073998 (Personal)
Permalink: http://viaf.org/viaf/56073998
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Farooqi
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I. Sadaf
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100 1 _ ‡a Farooqi, I. Sadaf
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100 1 _ ‡a Farooqi, I. Sadaf
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100 1 _
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Farooqi, I. Sadaf
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100 1 _
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Farooqi, I. Sadaf
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100 1 _ ‡a Farooqi, I. Sadaf
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100 1 _
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Farooqi, I. Sadaf,
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19..-....
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صدف فاروقي
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طبيبة استشارية بريطانية
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100 1 _ ‡a فاروقي، صدف
4xx's: Alternate Name Forms (5)
Works
| Title | Sources |
|---|---|
| Genetics of obesity syndromes |
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| Human SH2B1 mutations are associated with maladaptive behaviors and obesity |
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| Hyperphagia, severe obesity, impaired cognitive function, and hyperactivity associated with functional loss of one copy of the brain-derived neurotrophic factor (BDNF) gene |
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| Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis. |
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| Hypothalamic Reproductive Endocrine Pulse Generator Activity Independent of Neurokinin B and Dynorphin Signaling |
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| Iatrogenic chest pain: a case of 5-fluorouracil cardiotoxicity |
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| Increased body mass index is associated with specific regional alterations in brain structure |
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| Influence of leptin on arterial distensibility: a novel link between obesity and cardiovascular disease? |
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| Insulin resistance, high prevalence of diabetes, and cardiovascular risk in immigrant Asians |
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| Is leptin an important physiological regulator of CRP? |
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| Leptin regulates peripheral lipid metabolism primarily through central effects on food intake |
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| Leptin regulates striatal regions and human eating behavior |
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| Leptin substitution results in the induction of menstrual cycles in an adolescent with leptin deficiency and hypogonadotropic hypogonadism. |
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| Leptin therapy in a congenital leptin-deficient patient leads to acute and long-term changes in homeostatic, reward, and food-related brain areas. |
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| Lipid Metabolism and Survival Across the Frontotemporal Dementia-Amyotrophic Lateral Sclerosis Spectrum: Relationships to Eating Behavior and Cognition |
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| Long-term stabilization effects of leptin on brain functions in a leptin-deficient patient |
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| Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations |
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| Melanocortin-4 receptor signaling is required for weight loss after gastric bypass surgery |
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| A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism |
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| Modulation of blood pressure by central melanocortinergic pathways |
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| Molecular characterization of an interstitial deletion of 1p31.3 in a patient with obesity and psychiatric illness and a review of the literature |
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| Molecular Genetic Analysis of Normosmic Hypogonadotropic Hypogonadism in a Turkish Population: Identification and Detailed Functional Characterization of a Novel Mutation in the Gonadotropin-Releasing Hormone Receptor Gene |
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| Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesis |
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| Mutational analysis of the serotonin receptor 5HT2c in severe early-onset human obesity. |
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| Mutations in the amino-terminal region of proopiomelanocortin (POMC) in patients with early-onset obesity impair POMC sorting to the regulated secretory pathway |
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| Neural and behavioral effects of a novel mu opioid receptor antagonist in binge-eating obese people |
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| Neural deletion of Sh2b1 results in brain growth retardation and reactive aggression. |
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| Neural networks associated with body composition in frontotemporal dementia |
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| A New Drug Target for Type 2 Diabetes. |
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| A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. |
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| Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction |
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| A novel mutation in the leptin gene (W121X) in an Egyptian family. |
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| OBEDIS Core Variables Project: European Expert Guidelines on a Minimal Core Set of Variables to Include in Randomized, Controlled Clinical Trials of Obesity Interventions |
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| The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase |
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| Obesity associated genetic variation in FTO is associated with diminished satiety |
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| Obesity-associated melanocortin-4 receptor mutations are associated with changes in the brain response to food cues |
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| Obesity associated with increased brain age from midlife |
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| Obesity due to melanocortin 4 receptor (MC4R) deficiency is associated with increased linear growth and final height, fasting hyperinsulinemia, and incompletely suppressed growth hormone secretion |
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| Obesity genes-it's all about the parents! |
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| Oral glutamine increases circulating glucagon-like peptide 1, glucagon, and insulin concentrations in lean, obese, and type 2 diabetic subjects |
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| The orphan G protein-coupled receptor GPR139 is activated by the peptides: Adrenocorticotropic hormone (ACTH), α-, and β-melanocyte stimulating hormone (α-MSH, and β-MSH), and the conserved core motif HFRW. |
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| Oxytocin administration suppresses hypothalamic activation in response to visual food cues |
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| Palmitic Acid Hydroxystearic Acids Activate GPR40, Which Is Involved in Their Beneficial Effects on Glucose Homeostasis. |
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| Partial leptin deficiency and human adiposity. |
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| Pediatric Obesity-Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline. |
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| Pharmacological Chaperones Restore Function to MC4R Mutants Responsible for Severe Early-Onset Obesity |
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| A POMC variant implicates beta-melanocyte-stimulating hormone in the control of human energy balance |
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| Postprandial total ghrelin suppression is modulated by melanocortin signaling in humans |
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| Prevalence and functionality of paucimorphic and privateMC4Rmutations in a large, unselected European British population, scanned by meltMADGE |
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| Prevalence of loss-of-function FTO mutations in lean and obese individuals |
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| Prevalence of melanocortin-4 receptor deficiency in Europeans and their age-dependent penetrance in multigenerational pedigrees. |
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| Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue. |
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| ProxECAT: Proxy External Controls Association Test. A new case-control gene region association test using allele frequencies from public controls |
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| Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. |
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| Quantitative mass spectrometry for human melanocortin peptides in vitro and in vivo suggests prominent roles for β-MSH and desacetyl α-MSH in energy homeostasis |
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| A Quantitative Trait Locus on Chromosome 18q for Physical Activity and Dietary Intake in Hispanic Children* |
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| Rapid improvement of hepatic steatosis after initiation of leptin substitution in a leptin-deficient girl. |
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| Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood |
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| Rare variants in single-minded 1 (SIM1) areassociated with severe obesity. |
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| Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagia |
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| Role of melanocortin signalling in the preference for dietary macronutrients in human beings |
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| Screening the human prepro-orexin gene in a single-centre narcolepsy cohort |
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| Sequence variants in the melatonin-related receptor gene (GPR50) associate with circulating triglyceride and HDL levels |
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| Sequential alterations in haemorheology, endothelial dysfunction, platelet activation and thrombogenesis in relation to prognosis following acute stroke: The West Birmingham Stroke Project |
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| Serum ghrelin levels are inversely correlated with body mass index, age, and insulin concentrations in normal children and are markedly increased in Prader-Willi syndrome. |
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| Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene |
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| Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency |
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| The Sleep/Wake Cycle is Directly Modulated by Changes in Energy Balance |
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| Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency |
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| Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension. |
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| Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis |
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| Studies of the neuromedin U-2 receptor gene in human obesity: evidence for the existence of two ancestral forms of the receptor |
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| Studies of the SIM1 gene in relation to human obesity and obesity-related traits. |
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| Studying food reward and motivation in humans |
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| Sudden infant death syndrome among Asians in Britain |
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| TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency |
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| Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity |
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| Traversing the highs and lows of muslim marriage = Kayfa tataʻāmalu maʻa najāhāt wa-intikāsāt al-zawāj al-Islāmī |
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| Treating obesity: Does antagonism of NPY fit the bill? |
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| Triple H syndrome: a novel autoimmune endocrinopathy characterized by dysfunction of the hippocampus, hair follicle, and hypothalamic-pituitary adrenal axis |
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| Uncoupling protein 3 genetic variants in human obesity: the c-55t promoter polymorphism is negatively correlated with body mass index in a UK Caucasian population |
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| The V103I polymorphism of the MC4R gene and obesity: population based studies and meta-analysis of 29 563 individuals |
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| Wired for obesity? |
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