BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 38469147)

  • 1. Whole-exome sequencing combined with postoperative data identify c.1614dup (CAMKK2) as a novel candidate monogenic obesity variant.
    Wang Y; Yang C; Wen J; Ju L; Ren Z; Zhang T; Liu Y
    Front Endocrinol (Lausanne); 2024; 15():1334342. PubMed ID: 38469147
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Monogenic Obesity Mutations Lead to Less Weight Loss After Bariatric Surgery: a 6-Year Follow-Up Study.
    Li Y; Zhang H; Tu Y; Wang C; Di J; Yu H; Zhang P; Bao Y; Jia W; Yang J; Hu C
    Obes Surg; 2019 Apr; 29(4):1169-1173. PubMed ID: 30719650
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional analysis of an R311C variant of Ca
    Xy Ling N; Langendorf CG; Hoque A; Galic S; Loh K; Kemp BE; Gundlach AL; Oakhill JS; Scott JW
    Bipolar Disord; 2020 Dec; 22(8):841-848. PubMed ID: 32216002
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole exome sequencing reveals novel LEPR frameshift mutation in severely obese children from Western India.
    Bhatt A; Purani C; Bhargava P; Patel K; Agarbattiwala T; Puvar A; Shah K; Joshi CG; Dhamecha N; Prabhakar M; Joshi M
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00692. PubMed ID: 31070016
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted gene panel provides advantages over whole-exome sequencing for diagnosing obesity and diabetes mellitus.
    Yu H; Yu H; Zhang R; Peng D; Yan D; Gu Y; Bao Y; Jia W; Zhang H; Hu C
    J Mol Cell Biol; 2023 Nov; 15(6):. PubMed ID: 37327085
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification and Characteristics of Novel Mutations in Nonsyndromic Monogenic Obesity.
    Shi P; Shi Y; Liu X; Wang S; Yuan J; Zhao W; Fang L; Wang R; Yan F; Xu C
    Adv Biol (Weinh); 2023 Aug; 7(8):e2300061. PubMed ID: 37083215
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole exome sequencing in unexplained recurrent miscarriage families identified novel pathogenic genetic causes of euploid miscarriage.
    Wang X; Shi W; Zhao S; Gong D; Li S; Hu C; Chen ZJ; Li Y; Yan J
    Hum Reprod; 2023 May; 38(5):1003-1018. PubMed ID: 36864708
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data.
    Khan AO; Stapley RJ; Pike JA; Wijesinghe SN; Reyat JS; Almazni I; Machlus KR; Morgan NV;
    J Thromb Haemost; 2021 Jan; 19(1):262-268. PubMed ID: 33021027
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole exome sequencing reveals novel candidate gene variants for MODY.
    Yalçın Çapan Ö; Aydın N; Yılmaz T; Berber E
    Clin Chim Acta; 2020 Nov; 510():97-104. PubMed ID: 32645390
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid Obesity.
    Cooiman MI; Kleinendorst L; Aarts EO; Janssen IMC; van Amstel HKP; Blakemore AI; Hazebroek EJ; Meijers-Heijboer HJ; van der Zwaag B; Berends FJ; van Haelst MM
    Obes Surg; 2020 Feb; 30(2):470-477. PubMed ID: 31650404
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
    Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
    Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency.
    Bestetti I; Barbieri C; Sironi A; Specchia V; Yatsenko SA; De Donno MD; Caslini C; Gentilini D; Crippa M; Larizza L; Marozzi A; Rajkovic A; Toniolo D; Bozzetti MP; Finelli P
    Hum Reprod; 2021 Oct; 36(11):2975-2991. PubMed ID: 34480478
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing.
    Liao CY; Yu HW; Cheng CN; Chen JS; Lin CW; Chen PC; Shieh CC
    J Microbiol Immunol Infect; 2020 Feb; 53(1):99-105. PubMed ID: 29551298
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene.
    Goksen D; Evin F; Isik E; Ozen S; Atik T; Ozkinay F; Akcan N; Ozkan B; Buyukinan M; Nuri Ozbek M; Darcan S; Onay H
    Diabetes Res Clin Pract; 2023 Nov; 205():110953. PubMed ID: 37838154
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
    Warejko JK; Tan W; Daga A; Schapiro D; Lawson JA; Shril S; Lovric S; Ashraf S; Rao J; Hermle T; Jobst-Schwan T; Widmeier E; Majmundar AJ; Schneider R; Gee HY; Schmidt JM; Vivante A; van der Ven AT; Ityel H; Chen J; Sadowski CE; Kohl S; Pabst WL; Nakayama M; Somers MJG; Rodig NM; Daouk G; Baum M; Stein DR; Ferguson MA; Traum AZ; Soliman NA; Kari JA; El Desoky S; Fathy H; Zenker M; Bakkaloglu SA; Müller D; Noyan A; Ozaltin F; Cadnapaphornchai MA; Hashmi S; Hopcian J; Kopp JB; Benador N; Bockenhauer D; Bogdanovic R; Stajić N; Chernin G; Ettenger R; Fehrenbach H; Kemper M; Munarriz RL; Podracka L; Büscher R; Serdaroglu E; Tasic V; Mane S; Lifton RP; Braun DA; Hildebrandt F
    Clin J Am Soc Nephrol; 2018 Jan; 13(1):53-62. PubMed ID: 29127259
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models.
    Wang C; Seltzsam S; Zheng B; Wu CW; Nicolas-Frank C; Yousef K; Au KS; Mann N; Pantel D; Schneider S; Schierbaum L; Kitzler TM; Connaughton DM; Mao Y; Dai R; Nakayama M; Kari JA; El Desoky S; Shalaby M; Eid LA; Awad HS; Tasic V; Mane SM; Lifton RP; Baum MA; Shril S; Estrada CR; Hildebrandt F
    Am J Med Genet A; 2022 May; 188(5):1355-1367. PubMed ID: 35040250
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole Exome Sequencing in Early-onset Systemic Lupus Erythematosus.
    Batu ED; Koşukcu C; Taşkıran E; Sahin S; Akman S; Sözeri B; Ünsal E; Bilginer Y; Kasapcopur O; Alikaşifoğlu M; Ozen S
    J Rheumatol; 2018 Dec; 45(12):1671-1679. PubMed ID: 30008451
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
    Vivante A; Ityel H; Pode-Shakked B; Chen J; Shril S; van der Ven AT; Mann N; Schmidt JM; Segel R; Aran A; Zeharia A; Staretz-Chacham O; Bar-Yosef O; Raas-Rothschild A; Landau YE; Lifton RP; Anikster Y; Hildebrandt F
    Pediatr Nephrol; 2017 Dec; 32(12):2273-2282. PubMed ID: 28779239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impact of Genetic Variation on Human CaMKK2 Regulation by Ca
    O'Brien MT; Oakhill JS; Ling NX; Langendorf CG; Hoque A; Dite TA; Means AR; Kemp BE; Scott JW
    Sci Rep; 2017 Feb; 7():43264. PubMed ID: 28230171
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome Sequencing.
    Chang LH; Chi NF; Chen CY; Lin YS; Hsu SL; Tsai JY; Huang HC; Lin CJ; Chung CP; Tung CY; Jeng CJ; Lee YC; Liu YT; Lee IH
    Cell Mol Neurobiol; 2023 Aug; 43(6):2769-2783. PubMed ID: 36580209
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.