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Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice

Cell metabolism, 2014-05, Vol.19 (5), p.767-779

2014

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The metabolic conditioning of obesity: A review of the pathogenesis of obesity and the epigenetic pathways that "program" obesity from conception

Frontiers in endocrinology (Lausanne), 2022-10, Vol.13, p.1032491

2022

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Hypomorphism of Fto and Rpgrip1l causes obesity in mice

The Journal of clinical investigation, 2016-05, Vol.126 (5), p.1897-1910

2016

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Cut-like Homeobox 1 (CUX1) Regulates Expression of the Fat Mass and Obesity-associated and Retinitis Pigmentosa GTPase Regulator-interacting Protein-1-like (RPGRIP1L) Genes and Coordinates Leptin Receptor Signaling

The Journal of biological chemistry, 2011-01, Vol.286 (3), p.2155-2170

2011

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The Role of Leptin in the Development of Energy Homeostatic Systems and the Maintenance of Body Weight

Frontiers in physiology, 2021-12, Vol.12, p.789519-789519

2021

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Differentiation of hypothalamic-like neurons from human pluripotent stem cells

The Journal of clinical investigation, 2015-02, Vol.125 (2), p.796-808

2015

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FTO mediates cell-autonomous effects on adipogenesis and adipocyte lipid content by regulating gene expression via 6mA DNA modifications

Journal of lipid research, 2018-08, Vol.59 (8), p.1446-1460

2018

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Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes

Human molecular genetics, 2017-12, Vol.26 (23), p.4606-4616

2017

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Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry

Journal of Pediatric Endocrinology and Metabolism, 2021-05, Vol.34 (5), p.633-638

2021

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Genetic loss of SH2B3 in acute lymphoblastic leukemia

Blood, 2013-10, Vol.122 (14), p.2425-2432

2013

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Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy

American journal of human genetics, 2016-03, Vol.98 (3), p.562-570

2016

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DMSO increases efficiency of genome editing at two non-coding loci

PloS one, 2018-06, Vol.13 (6), p.e0198637

2018

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A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

American journal of human genetics, 2013-06, Vol.92 (6), p.996-1000

2013

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Effects of ambient temperature on adaptive thermogenesis during maintenance of reduced body weight in mice

American journal of physiology. Regulatory, integrative and comparative physiology, 2012-08, Vol.303 (4), p.R438-R448

2012

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Biallelic Loss-of-Function Variants in BICD1 Are Associated with Peripheral Neuropathy and Hearing Loss

International journal of molecular sciences, 2023-05, Vol.24 (10), p.8897

2023

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Energy homeostasis in leptin deficient Lepob/ob mice

PloS one, 2017, Vol.12 (12), p.e0189784-e0189784

2017

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ILDR2 has a negligible role in hepatic steatosis

PloS one, 2018-05, Vol.13 (5), p.e0197548-e0197548

2018

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ZNF70, a novel ILDR2-interacting protein, contributes to the regulation of HES1 gene expression

Biochemical and biophysical research communications, 2016-09, Vol.477 (4), p.712-716

2016

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A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis

Journal of inherited metabolic disease, 2011-10, Vol.34 (5), p.1013-1022

2011

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Rare predicted loss of function alleles in Bassoon (BSN) are associated with obesity

Npj genomic medicine, 2023-10, Vol.8 (1), p.33-33, Article 33

2023

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Weight Perturbation Alters Leptin Signal Transduction in a Region-Specific Manner throughout the Brain

PloS one, 2017-01, Vol.12 (1), p.e0168226-e0168226

2017

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178-LB: Association of Pregnancy Oral Glucose Tolerance Test (OGTT) Glucose Response with Metabolic Profile in Mother and Child—Hyperglycemia and Adverse Pregnancy Outcomes Follow-up Study (HAPO-FUS)

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

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ILDR2: an endoplasmic reticulum resident molecule mediating hepatic lipid homeostasis

PloS one, 2013-06, Vol.8 (6), p.e67234-e67234

2013

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Neurodevelopmental Programming of Adiposity: Contributions to Obesity Risk

Endocrine reviews, 2024-03, Vol.45 (2), p.253-280

2024

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Absence epilepsy in apathetic , a spontaneous mutant mouse lacking the h channel subunit, HCN2

Neurobiology of disease, 2009-03, Vol.33 (3), p.499-508

2009

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Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice

The metabolic conditioning of obesity: A review of the pathogenesis of obesity and the epigenetic pathways that "program" obesity from conception

Hypomorphism of Fto and Rpgrip1l causes obesity in mice

Cut-like Homeobox 1 (CUX1) Regulates Expression of the Fat Mass and Obesity-associated and Retinitis Pigmentosa GTPase Regulator-interacting Protein-1-like (RPGRIP1L) Genes and Coordinates Leptin Receptor Signaling

The Role of Leptin in the Development of Energy Homeostatic Systems and the Maintenance of Body Weight

Differentiation of hypothalamic-like neurons from human pluripotent stem cells

FTO mediates cell-autonomous effects on adipogenesis and adipocyte lipid content by regulating gene expression via 6mA DNA modifications

Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes

Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry

Genetic loss of SH2B3 in acute lymphoblastic leukemia

Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy

DMSO increases efficiency of genome editing at two non-coding loci

A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

Effects of ambient temperature on adaptive thermogenesis during maintenance of reduced body weight in mice

Biallelic Loss-of-Function Variants in BICD1 Are Associated with Peripheral Neuropathy and Hearing Loss

Energy homeostasis in leptin deficient Lepob/ob mice

ILDR2 has a negligible role in hepatic steatosis

ZNF70, a novel ILDR2-interacting protein, contributes to the regulation of HES1 gene expression

A complete deficiency of Hyaluronoglucosaminidase 1 (HYAL1) presenting as familial juvenile idiopathic arthritis

Rare predicted loss of function alleles in Bassoon (BSN) are associated with obesity

Weight Perturbation Alters Leptin Signal Transduction in a Region-Specific Manner throughout the Brain

178-LB: Association of Pregnancy Oral Glucose Tolerance Test (OGTT) Glucose Response with Metabolic Profile in Mother and Child—Hyperglycemia and Adverse Pregnancy Outcomes Follow-up Study (HAPO-FUS)

ILDR2: an endoplasmic reticulum resident molecule mediating hepatic lipid homeostasis

Neurodevelopmental Programming of Adiposity: Contributions to Obesity Risk

Absence epilepsy in apathetic , a spontaneous mutant mouse lacking the h channel subunit, HCN2

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