These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 26443248)

  • 1. Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome Sequencing.
    Mehrjoo Z; Akbari MR; Abedini SS; Vaziri S; Kahrizi K; Najmabadi H
    Arch Iran Med; 2015 Oct; 18(10):643-69. PubMed ID: 26443248
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Contribution of Iran in Elucidating the Genetic Causes of Autosomal Recessive Intellectual Disability.
    Ataei R; Khoshbakht S; Beheshtian M; Abedini SS; Behravan H; Esmaeili Dizghandi S; Godratpour F; Mirzaei S; Bahrami F; Akbari M; Keshavarzi F; Kahrizi K; Najmabadi H
    Arch Iran Med; 2019 Aug; 22(8):461-471. PubMed ID: 31679349
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Effect of inbreeding on intellectual disability revisited by trio sequencing.
    Kahrizi K; Hu H; Hosseini M; Kalscheuer VM; Fattahi Z; Beheshtian M; Suckow V; Mohseni M; Lipkowitz B; Mehvari S; Mehrjoo Z; Akhtarkhavari T; Ghaderi Z; Rahimi M; Arzhangi S; Jamali P; Falahat Chian M; Nikuei P; Sabbagh Kermani F; Sadeghinia F; Jazayeri R; Tonekaboni SH; Khoshaeen A; Habibi H; Pourfatemi F; Mojahedi F; Khodaie-Ardakani MR; Najafipour R; Wienker TF; Najmabadi H; Ropers HH
    Clin Genet; 2019 Jan; 95(1):151-159. PubMed ID: 30315573
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
    Ahmed I; Rafiq MA; Vincent JB; Bhatti A; Ayub M; John P
    Acta Neuropsychiatr; 2015 Feb; 27(1):38-47. PubMed ID: 25434728
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
    Harripaul R; Vasli N; Mikhailov A; Rafiq MA; Mittal K; Windpassinger C; Sheikh TI; Noor A; Mahmood H; Downey S; Johnson M; Vleuten K; Bell L; Ilyas M; Khan FS; Khan V; Moradi M; Ayaz M; Naeem F; Heidari A; Ahmed I; Ghadami S; Agha Z; Zeinali S; Qamar R; Mozhdehipanah H; John P; Mir A; Ansar M; French L; Ayub M; Vincent JB
    Mol Psychiatry; 2018 Apr; 23(4):973-984. PubMed ID: 28397838
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The
    Cheraghi S; Moghbelinejad S; Najmabadi H; Kahrizi K; Najafipour R
    Arch Iran Med; 2021 Oct; 24(10):747-751. PubMed ID: 34816696
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identifying genes responsible for intellectual disability in consanguineous families.
    Iqbal Z; van Bokhoven H
    Hum Hered; 2014; 77(1-4):150-60. PubMed ID: 25060278
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.
    Davarniya B; Hu H; Kahrizi K; Musante L; Fattahi Z; Hosseini M; Maqsoud F; Farajollahi R; Wienker TF; Ropers HH; Najmabadi H
    PLoS One; 2015; 10(8):e0129631. PubMed ID: 26308914
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetics of intellectual disability in consanguineous families.
    Hu H; Kahrizi K; Musante L; Fattahi Z; Herwig R; Hosseini M; Oppitz C; Abedini SS; Suckow V; Larti F; Beheshtian M; Lipkowitz B; Akhtarkhavari T; Mehvari S; Otto S; Mohseni M; Arzhangi S; Jamali P; Mojahedi F; Taghdiri M; Papari E; Soltani Banavandi MJ; Akbari S; Tonekaboni SH; Dehghani H; Ebrahimpour MR; Bader I; Davarnia B; Cohen M; Khodaei H; Albrecht B; Azimi S; Zirn B; Bastami M; Wieczorek D; Bahrami G; Keleman K; Vahid LN; Tzschach A; Gärtner J; Gillessen-Kaesbach G; Varaghchi JR; Timmermann B; Pourfatemi F; Jankhah A; Chen W; Nikuei P; Kalscheuer VM; Oladnabi M; Wienker TF; Ropers HH; Najmabadi H
    Mol Psychiatry; 2019 Jul; 24(7):1027-1039. PubMed ID: 29302074
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of disease-causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families.
    Beheshtian M; Fattahi Z; Fadaee M; Vazehan R; Jamali P; Parsimehr E; Kamgar M; Zonooz MF; Mahdavi SS; Kalhor Z; Arzhangi S; Abedini SS; Kermani FS; Mojahedi F; Kalscheuer VM; Ropers HH; Kariminejad A; Najmabadi H; Kahrizi K
    Clin Genet; 2019 Jun; 95(6):718-725. PubMed ID: 30950035
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.
    Rafiullah R; Aslamkhan M; Paramasivam N; Thiel C; Mustafa G; Wiemann S; Schlesner M; Wade RC; Rappold GA; Berkel S
    J Med Genet; 2016 Feb; 53(2):138-44. PubMed ID: 26566883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort.
    Zare Ashrafi F; Akhtarkhavari T; Fattahi Z; Asadnezhad M; Beheshtian M; Arzhangi S; Najmabadi H; Kahrizi K
    Arch Iran Med; 2023 Apr; 26(4):186-197. PubMed ID: 38301078
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability.
    Riazuddin S; Hussain M; Razzaq A; Iqbal Z; Shahzad M; Polla DL; Song Y; van Beusekom E; Khan AA; Tomas-Roca L; Rashid M; Zahoor MY; Wissink-Lindhout WM; Basra MAR; Ansar M; Agha Z; van Heeswijk K; Rasheed F; Van de Vorst M; Veltman JA; Gilissen C; Akram J; Kleefstra T; Assir MZ; ; Grozeva D; Carss K; Raymond FL; O'Connor TD; Riazuddin SA; Khan SN; Ahmed ZM; de Brouwer APM; van Bokhoven H; Riazuddin S
    Mol Psychiatry; 2017 Nov; 22(11):1604-1614. PubMed ID: 27457812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability.
    Santos-Cortez RLP; Khan V; Khan FS; Mughal ZU; Chakchouk I; Lee K; Rasheed M; Hamza R; Acharya A; Ullah E; Saqib MAN; Abbe I; Ali G; Hassan MJ; Khan S; Azeem Z; Ullah I; Bamshad MJ; Nickerson DA; Schrauwen I; Ahmad W; Ansar M; Leal SM
    Hum Genet; 2018 Sep; 137(9):735-752. PubMed ID: 30167849
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel variants underlying autosomal recessive intellectual disability in Pakistani consanguineous families.
    Ilyas M; Efthymiou S; Salpietro V; Noureen N; Zafar F; Rauf S; Mir A; Houlden H
    BMC Med Genet; 2020 Mar; 21(1):59. PubMed ID: 32209057
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability in Iranian consanguineous families.
    Moudi M; Vahidi Mehrjardi MY; Hozhabri H; Metanat Z; Kalantar SM; Taheri M; Ghasemi N; Dehghani M
    J Clin Lab Anal; 2022 Feb; 36(2):e24241. PubMed ID: 35019165
    [TBL] [Abstract][Full Text] [Related]  

  • 17. First steps in exploring prospective exome sequencing of consanguineous couples.
    Teeuw M; Waisfisz Q; Zwijnenburg PJ; Sistermans EA; Weiss MM; Henneman L; ten Kate LP; Cornel MC; Meijers-Heijboer H
    Eur J Med Genet; 2014; 57(11-12):613-6. PubMed ID: 25281896
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with Ataxia.
    Jazayeri R; Hu H; Fattahi Z; Musante L; Abedini SS; Hosseini M; Wienker TF; Ropers HH; Najmabadi H; Kahrizi K
    Arch Iran Med; 2015 Oct; 18(10):670-82. PubMed ID: 26443249
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus.
    Alazami AM; Hijazi H; Al-Dosari MS; Shaheen R; Hashem A; Aldahmesh MA; Mohamed JY; Kentab A; Salih MA; Awaji A; Masoodi TA; Alkuraya FS
    J Med Genet; 2013 Jul; 50(7):425-30. PubMed ID: 23620220
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exome sequencing identifies three novel candidate genes implicated in intellectual disability.
    Agha Z; Iqbal Z; Azam M; Ayub H; Vissers LE; Gilissen C; Ali SH; Riaz M; Veltman JA; Pfundt R; van Bokhoven H; Qamar R
    PLoS One; 2014; 9(11):e112687. PubMed ID: 25405613
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.