Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Affected individuals have distinct physical features, and growth hormone (GH) deficiency occurs in some individuals with PWS. 31782896

2020

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Growth hormone (GH) replacement positively influences stature and body composition in PWS. 31698873

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Methods A total of 14 patients with PWS started treatment with GH under the age of 2 years and were followed over a 2-year period. 31271556

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Recent evidence indicates healthy outcomes of weight and height can be achieved with growth hormone therapy and dietary restriction and should be the current target for all individuals with PWS. 31257692

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Patients with PWS present with a decreased physical performance and impaired cardiorespiratory (maximal oxygen consumption, heart rate recovery after exercise) and hormonal (growth hormone release) responses to exercise. 30788853

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass index. 31313492

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE The present study demonstrated favorable evolution of hip radiographic parameters in the PWS population treated with growth hormone early in development. 31479030

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Human Prader-Willi syndrome (PWS) is characterised by impairments of multiple systems including the growth hormone (GH) axis and skeletal growth. 31454785

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE This study aimed to investigate the GH/insulin-like growth factor (IGF-I) axis and the prevalence of GHD in previously GH-treated young adults with PWS. 30973645

2019

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Increased sensitivity may accelerate spinal growth and contribute to scoliosis, particularly in GH-deficient and treated populations such as Prader-Willi syndrome (PWS). 29273483

2018

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Twenty-seven young adults with PWS were stratified for gender and BMI and then randomly and blindly assigned to receive GH (0.67 mg/m<sup>2</sup> /day) or placebo for 1 year, after which they crossed over to the alternative treatment for another year. 29418016

2018

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Growth hormone (GH) therapy in Poland is conducted within the nationwide framework of the Therapeutic Programme: "Treatment of Prader-Willi Syndrome". 30209801

2018

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE A 1 year, 1-month-old boy with Prader-Willi syndrome treated with growth hormone had ITGCN in both cryptorchid testes. 27606906

2017

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE To investigate the effects of GH vs placebo on metabolic health, in young adults with PWS who were GH-treated for many years during childhood and had attained adult height (AH). 27689944

2017

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE We also reported the onset of diabetes mellitus (DM), scoliosis, and respiratory problems in patients with Prader-Willi syndrome who were treated with GH. 28516752

2017

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE There were no differences in rates of aspiration for gender, genetic subtype, or GH use.A high incidence of aspiration was identified indicating swallow dysfunction may frequently be present in infants with PWS. 29390364

2017

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE This study emphasizes the importance of evaluating bone mineralization in individuals with PWS and the beneficial effects of prolonged treatment with growth hormone. 24515997

2014

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Therefore, cessation of GH therapy in PWS patients worsened BMI. 24443368

2014

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE The presence of the d3 allele and its impact on growth and medical care of individuals with PWS while on GH therapy should be further investigated. 23696513

2013

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE We evaluated the GH secretion in pediatric patients with PWS. 22585665

2012

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Paediatric GH is currently licensed in six different conditions: growth hormone deficiency (GHD), Turner syndrome (TS), small for gestational age (SGA), Prader-Willi-syndrome (PWS), chronic renal insufficiency (CRI), and short stature due to SHOX deficiency; all of these have been ratified by the most recent (2010) NICE review. 21540481

2012

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Curves for height/length, weight and body mass index were constructed and compared between Prader-Willi syndrome patients treated with and without growth hormone to determine how growth hormone treatment affected body composition. 22948460

2012

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 Biomarker BEFREE Growth hormone secretion among adult patients with Prader-Willi syndrome due to different genetic subtypes. 20651469

2012

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE However, patients with PWS carrying a d3 allele had significantly greater height standard deviation scores (SDS) (P = 0.025) and higher insulin-like growth factor I (IGF-I) level (P = 0.041), although the age at the start of GH therapy, weight, BMI, and body fat were not different. 22052808

2011

Entrez Id: 2688
Gene Symbol: GH1
GH1
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome
0.100 GeneticVariation BEFREE Thirty children with PWS (median age 7.1 yr, 18 males, 12 females) that were being treated with GH and 32 obese children not receiving GH treatment (median age 9.1 yr, 15 males, 17 females) for comparison were enrolled. 20061428

2010