119 related articles for article (PubMed ID: 22791212)
1. Variability in laboratory reporting practices for regions of homozygosity indicating parental relatedness as identified by SNP microarray testing.
Grote L; Myers M; Lovell A; Saal H; Lipscomb Sund K
Genet Med; 2012 Dec; 14(12):971-6. PubMed ID: 22791212
[TBL] [Abstract][Full Text] [Related]
2. Variable approaches to genetic counseling for microarray regions of homozygosity associated with parental relatedness.
Grote L; Myers M; Lovell A; Saal H; Sund KL
Am J Med Genet A; 2014 Jan; 164A(1):87-98. PubMed ID: 24243712
[TBL] [Abstract][Full Text] [Related]
3. Detection and reporting of homozygosity associated with consanguinity in the clinical laboratory.
Sund KL; Rehder CW
Hum Hered; 2014; 77(1-4):217-24. PubMed ID: 25060286
[TBL] [Abstract][Full Text] [Related]
4. Three clinical experiences with SNP array results consistent with parental incest: a narrative with lessons learned.
Helm BM; Langley K; Spangler B; Vergano S
J Genet Couns; 2014 Aug; 23(4):489-95. PubMed ID: 24222483
[TBL] [Abstract][Full Text] [Related]
5. Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships.
Sund KL; Zimmerman SL; Thomas C; Mitchell AL; Prada CE; Grote L; Bao L; Martin LJ; Smolarek TA
Genet Med; 2013 Jan; 15(1):70-8. PubMed ID: 22858719
[TBL] [Abstract][Full Text] [Related]
6. Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG).
Gonzales PR; Andersen EF; Brown TR; Horner VL; Horwitz J; Rehder CW; Rudy NL; Robin NH; Thorland EC; On Behalf Of The Acmg Laboratory Quality Assurance Committee
Genet Med; 2022 Feb; 24(2):255-261. PubMed ID: 34906464
[TBL] [Abstract][Full Text] [Related]
7. Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families.
Delgado F; Tabor HK; Chow PM; Conta JH; Feldman KW; Tsuchiya KD; Beck AE
Genet Med; 2015 May; 17(5):400-4. PubMed ID: 25232848
[TBL] [Abstract][Full Text] [Related]
8. The perils of SNP microarray testing: uncovering unexpected consanguinity.
Tarini BA; Konczal LL; Goldenberg AJ; Goldman EB; McCandless SE
Pediatr Neurol; 2013 Jul; 49(1):50-3. PubMed ID: 23827427
[TBL] [Abstract][Full Text] [Related]
9. Chromosomal microarray in a highly consanguineous population: diagnostic yield, utility of regions of homozygosity, and novel mutations.
Alabdullatif MA; Al Dhaibani MA; Khassawneh MY; El-Hattab AW
Clin Genet; 2017 Apr; 91(4):616-622. PubMed ID: 27717089
[TBL] [Abstract][Full Text] [Related]
10. Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients.
Wen J; Chai H; Grommisch B; DiAdamo A; Dykas D; Ma D; Popa A; Zhao C; Spencer-Manzon M; Jiang YH; McGrath J; Li P; Bale A; Zhang H
Am J Med Genet A; 2022 Jun; 188(6):1728-1738. PubMed ID: 35199448
[TBL] [Abstract][Full Text] [Related]
11. Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility.
Wang JC; Ross L; Mahon LW; Owen R; Hemmat M; Wang BT; El Naggar M; Kopita KA; Randolph LM; Chase JM; Matas Aguilera MJ; Siles JL; Church JA; Hauser N; Shen JJ; Jones MC; Wierenga KJ; Jiang Z; Haddadin M; Boyar FZ; Anguiano A; Strom CM; Sahoo T
Eur J Hum Genet; 2015 May; 23(5):663-71. PubMed ID: 25118026
[TBL] [Abstract][Full Text] [Related]
12. Diagnostic implications of excessive homozygosity detected by SNP-based microarrays: consanguinity, uniparental disomy, and recessive single-gene mutations.
Kearney HM; Kearney JB; Conlin LK
Clin Lab Med; 2011 Dec; 31(4):595-613, ix. PubMed ID: 22118739
[TBL] [Abstract][Full Text] [Related]
13. Identification of incestuous parental relationships by SNP-based DNA microarrays.
Schaaf CP; Scott DA; Wiszniewska J; Beaudet AL
Lancet; 2011 Feb; 377(9765):555-6. PubMed ID: 21315943
[No Abstract] [Full Text] [Related]
14. American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
Rehder CW; David KL; Hirsch B; Toriello HV; Wilson CM; Kearney HM
Genet Med; 2013 Feb; 15(2):150-2. PubMed ID: 23328890
[TBL] [Abstract][Full Text] [Related]
15. Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity.
Ben Halim N; Nagara M; Regnault B; Hsouna S; Lasram K; Kefi R; Azaiez H; Khemira L; Saidane R; Ammar SB; Besbes G; Weil D; Petit C; Abdelhak S; Romdhane L
Ann Hum Genet; 2015 Nov; 79(6):402-17. PubMed ID: 26420437
[TBL] [Abstract][Full Text] [Related]
16. A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.
O'Daniel JM; McLaughlin HM; Amendola LM; Bale SJ; Berg JS; Bick D; Bowling KM; Chao EC; Chung WK; Conlin LK; Cooper GM; Das S; Deignan JL; Dorschner MO; Evans JP; Ghazani AA; Goddard KA; Gornick M; Farwell Hagman KD; Hambuch T; Hegde M; Hindorff LA; Holm IA; Jarvik GP; Knight Johnson A; Mighion L; Morra M; Plon SE; Punj S; Richards CS; Santani A; Shirts BH; Spinner NB; Tang S; Weck KE; Wolf SM; Yang Y; Rehm HL
Genet Med; 2017 May; 19(5):575-582. PubMed ID: 27811861
[TBL] [Abstract][Full Text] [Related]
17. Analytical validation and chromosomal distribution of regions of homozygosity by oligonucleotide array comparative genomic hybridization from normal prenatal and postnatal case series.
Wen J; Comerford K; Xu Z; Wu W; Amato K; Grommisch B; DiAdamo A; Xu F; Chai H; Li P
Mol Cytogenet; 2019; 12():12. PubMed ID: 30886647
[TBL] [Abstract][Full Text] [Related]
18. How to study runs of homozygosity using PLINK? A guide for analyzing medium density SNP data in livestock and pet species.
Meyermans R; Gorssen W; Buys N; Janssens S
BMC Genomics; 2020 Jan; 21(1):94. PubMed ID: 31996125
[TBL] [Abstract][Full Text] [Related]
19. Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy.
Santoro SL; Hashimoto S; McKinney A; Mihalic Mosher T; Pyatt R; Reshmi SC; Astbury C; Hickey SE
Cytogenet Genome Res; 2017; 152(2):105-109. PubMed ID: 28746920
[TBL] [Abstract][Full Text] [Related]
20. Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray.
Fan YS; Ouyang X; Peng J; Sacharow S; Tekin M; Barbouth D; Bodamer O; Yusupov R; Navarrete C; Heller AH; Pena SDj
Mol Cytogenet; 2013 Sep; 6(1):38. PubMed ID: 24053112
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
