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For: Qiao Y, Wen J, Tang F, Martell S, Shomer N, Leung PC, Stephenson MD, Rajcan-Separovic E. Whole exome sequencing in recurrent early pregnancy loss. Mol Hum Reprod. 2016;22:364-372. [PMID: 26826164 DOI: 10.1093/molehr/gaw008] [Cited by in Crossref: 33] [Cited by in F6Publishing: 29] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Dong Z, Yan J, Xu F, Yuan J, Jiang H, Wang H, Chen H, Zhang L, Ye L, Xu J, Shi Y, Yang Z, Cao Y, Chen L, Li Q, Zhao X, Li J, Chen A, Zhang W, Wong HG, Qin Y, Zhao H, Chen Y, Li P, Ma T, Wang WJ, Kwok YK, Jiang Y, Pursley AN, Chung JPW, Hong Y, Kristiansen K, Yang H, Piña-Aguilar RE, Leung TY, Cheung SW, Morton CC, Choy KW, Chen ZJ. Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage. Am J Hum Genet 2019;105:1102-11. [PMID: 31679651 DOI: 10.1016/j.ajhg.2019.10.003] [Cited by in Crossref: 31] [Cited by in F6Publishing: 21] [Article Influence: 10.3] [Reference Citation Analysis]
2 Feichtinger M, Reiner A, Hartmann B, Philipp T. Embryoscopy and karyotype findings of repeated miscarriages in recurrent pregnancy loss and spontaneous pregnancy loss. J Assist Reprod Genet 2018;35:1401-6. [PMID: 29916100 DOI: 10.1007/s10815-018-1226-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
3 Westerfield LE, Braxton AA, Walkiewicz M. Prenatal Diagnostic Exome Sequencing: a Review. Curr Genet Med Rep 2017;5:75-83. [DOI: 10.1007/s40142-017-0120-y] [Cited by in Crossref: 3] [Article Influence: 0.6] [Reference Citation Analysis]
4 Massalska D, Zimowski JG, Bijok J, Pawelec M, Czubak-barlik M, Jakiel G, Roszkowski T. First trimester pregnancy loss: Clinical implications of genetic testing: Pregnancy loss and genetic testing. J Obstet Gynaecol Res 2017;43:23-9. [DOI: 10.1111/jog.13179] [Cited by in Crossref: 18] [Cited by in F6Publishing: 14] [Article Influence: 3.0] [Reference Citation Analysis]
5 Zhao S, Lu J, Chen Y, Wang Z, Cao J, Dong Y. Exploration of the potential roles of m6A regulators in the uterus in pregnancy and infertility. J Reprod Immunol 2021;146:103341. [PMID: 34116483 DOI: 10.1016/j.jri.2021.103341] [Reference Citation Analysis]
6 Najafi K, Mehrjoo Z, Ardalani F, Ghaderi-Sohi S, Kariminejad A, Kariminejad R, Najmabadi H. Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities. Sci Rep 2021;11:6952. [PMID: 33772059 DOI: 10.1038/s41598-021-86309-9] [Reference Citation Analysis]
7 Pan H, Xiang H, Wang J, Wei Z, Zhou Y, Liu B, Li T, Ma X, Cao Y, Wang B. CAPS Mutations Are Potentially Associated with Unexplained Recurrent Pregnancy Loss. The American Journal of Pathology 2019;189:124-31. [DOI: 10.1016/j.ajpath.2018.09.010] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
8 Guo W, Zhu X, Yan L, Qiao J. The present and future of whole-exome sequencing in studying and treating human reproductive disorders. Journal of Genetics and Genomics 2018;45:517-25. [DOI: 10.1016/j.jgg.2018.08.004] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
9 Robbins SM, Thimm MA, Valle D, Jelin AC. Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes. J Assist Reprod Genet 2019;36:1539-48. [PMID: 31273585 DOI: 10.1007/s10815-019-01499-6] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 4.7] [Reference Citation Analysis]
10 Qiao Y, Bagheri H, Tang F, Badduke C, Martell S, Lewis SME, Robinson W, Connolly MB, Arbour L, Rajcan-Separovic E. Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. Eur J Med Genet 2019;62:103-8. [PMID: 29908350 DOI: 10.1016/j.ejmg.2018.06.010] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
11 Lynch MT, Maloney KA, Pollin TI, Streeten EA, Puffenberger EG, Strauss KA, Shuldiner AR, Mitchell BD; Regeneron Genetics Center. Impact of parental relatedness on reproductive outcomes among the Old Order Amish of Lancaster County. Am J Med Genet A 2022. [PMID: 35442562 DOI: 10.1002/ajmg.a.62757] [Reference Citation Analysis]
12 Li Y, Wang R, Wang M, Huang W, Liu C, Fang Z, Liao S, Jin L. RNA Sequencing of Decidua Reveals Differentially Expressed Genes in Recurrent Pregnancy Loss. Reprod Sci 2021;28:2261-9. [DOI: 10.1007/s43032-021-00482-w] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Wang MZ, Lin FQ, Li M, He D, Yu QH, Yang XX, Wu YS. Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage. Med Sci Monit 2017;23:5550-7. [PMID: 29162795 DOI: 10.12659/msm.905094] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
14 Kline J, Vardarajan B, Abhyankar A, Kytömaa S, Levin B, Sobreira N, Tang A, Thomas-Wilson A, Zhang R, Jobanputra V. Embryonic lethal genetic variants and chromosomally normal pregnancy loss. Fertil Steril 2021;116:1351-8. [PMID: 34756330 DOI: 10.1016/j.fertnstert.2021.06.039] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Fan L, Wu J, Wu Y, Shi X, Xin X, Li S, Zeng W, Deng D, Feng L, Chen S, Xiao J. Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation Sequencing. Front Genet 2020;11:545856. [PMID: 33193619 DOI: 10.3389/fgene.2020.545856] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
16 Hochstenbach R, van Binsbergen E, Schuring-Blom H, Buijs A, Ploos van Amstel HK. A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing. Eur J Med Genet 2019;62:103543. [PMID: 30248410 DOI: 10.1016/j.ejmg.2018.09.010] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
17 Rajcan-Separovic E. Next generation sequencing in recurrent pregnancy loss-approaches and outcomes. Eur J Med Genet 2020;63:103644. [PMID: 30991114 DOI: 10.1016/j.ejmg.2019.04.001] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 3.7] [Reference Citation Analysis]
18 Xu Q, Chan Y, Feng Y, Zhu B, Yang B, Zhu S, Su L, Zou L, Feng N, Li Y. Factors associated with fetal karyotype in spontaneous abortion: a case-case study. BMC Pregnancy Childbirth 2022;22. [DOI: 10.1186/s12884-022-04491-8] [Reference Citation Analysis]
19 Qiao Y, Badduke C, Tang F, Cowieson D, Martell S, Lewis SME, Peñaherrera MS, Robinson WP, Volchuk A, Rajcan-separovic E. Whole exome sequencing of families with 1q21.1 microdeletion or microduplication. Am J Med Genet 2017;173:1782-91. [DOI: 10.1002/ajmg.a.38247] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
20 Colley E, Hamilton S, Smith P, Morgan NV, Coomarasamy A, Allen S. Potential genetic causes of miscarriage in euploid pregnancies: a systematic review. Human Reproduction Update 2019;25:452-72. [DOI: 10.1093/humupd/dmz015] [Cited by in Crossref: 32] [Cited by in F6Publishing: 23] [Article Influence: 10.7] [Reference Citation Analysis]
21 Gourhant L, Bocher O, De Saint Martin L, Ludwig TE, Boland A, Deleuze JF, Merviel P, Dupré PF, Lemarié CA, Couturaud F, Le Maréchal C, Génin E, Pasquier E. Whole exome sequencing, a hypothesis-free approach to investigate recurrent early miscarriage. Reprod Biomed Online 2021;42:789-98. [PMID: 33658156 DOI: 10.1016/j.rbmo.2021.01.008] [Reference Citation Analysis]
22 Carey AZ, Blue NR, Varner MW, Page JM, Chaiyakunapruk N, Quinlan AR, Branch DW, Silver RM, Workalemahu T. A Systematic Review to Guide Future Efforts in the Determination of Genetic Causes of Pregnancy Loss. Front Reprod Health 2021;3:770517. [DOI: 10.3389/frph.2021.770517] [Reference Citation Analysis]
23 Schmidts M, Mitchison HM. Severe skeletal abnormalities caused by defects in retrograde intraflagellar transport dyneins. Dyneins. Elsevier; 2018. pp. 356-401. [DOI: 10.1016/b978-0-12-809470-9.00015-1] [Cited by in Crossref: 5] [Article Influence: 1.3] [Reference Citation Analysis]
24 Xiang H, Wang C, Pan H, Hu Q, Wang R, Xu Z, Li T, Su Y, Ma X, Cao Y, Wang B. Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort. Front Genet 2021;12:746082. [PMID: 34925444 DOI: 10.3389/fgene.2021.746082] [Reference Citation Analysis]
25 Wang H, Yuan D, Wang S, Luo L, Zhang Y, Ye J, Zhu K. Cytogenetic and genetic investigation of miscarriage cases in Eastern China. J Matern Fetal Neonatal Med 2020;33:3385-90. [PMID: 30741046 DOI: 10.1080/14767058.2019.1572738] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
26 Kasak L, Rull K, Laan M. Genetics and Genomics of Recurrent Pregnancy Loss. Human Reproductive and Prenatal Genetics. Elsevier; 2019. pp. 463-94. [DOI: 10.1016/b978-0-12-813570-9.00021-8] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
27 Fatemi N, Ray PF, Ramezanali F, Shahani T, Amiri-Yekta A, Kherraf ZE, Cazin C, Almadani N, Varkiani M, Sarmadi S, Sodeifi N, Gourabi H, Biglari A, Totonchi M. KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole. Eur J Obstet Gynecol Reprod Biol 2021;259:100-4. [PMID: 33639414 DOI: 10.1016/j.ejogrb.2021.02.006] [Reference Citation Analysis]
28 Ali Alghamdi M, Alrasheedi A, Alghamdi E, Adly N, AlAali WY, Alhashem A, Alshahrani A, Shamseldin H, Alkuraya FS, Alfadhel M. Molecular autopsy by proxy in preconception counseling. Clin Genet 2021;100:678-91. [PMID: 34406647 DOI: 10.1111/cge.14049] [Reference Citation Analysis]
29 Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609 [PMID: 33728303 DOI: 10.12998/wjcc.v9.i7.1600] [Reference Citation Analysis]
30 Lisova KM, Kalinovska IV, Pryimak SH, Tokar PY, Varlas VN. Changes in the level of fetoplacental complex hormones in pregnant women with miscarriage. J Med Life 2021;14:487-91. [PMID: 34621371 DOI: 10.25122/jml-2021-0089] [Reference Citation Analysis]
31 Quintero-Ronderos P, Laissue P. Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches. Reprod Sci 2019;:1933719119831769. [PMID: 30879428 DOI: 10.1177/1933719119831769] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
32 Wang Y, Cheng Q, Meng L, Luo C, Hu H, Zhang J, Cheng J, Xu T, Jiang T, Liang D, Hu P, Xu Z. Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study: Clinical application of SNP array analysis in first-trimester pregnancy loss. Clin Genet 2017;91:849-58. [DOI: 10.1111/cge.12926] [Cited by in Crossref: 38] [Cited by in F6Publishing: 36] [Article Influence: 6.3] [Reference Citation Analysis]
33 Kar B, Catherine B L. Genetic Factors Associated With Recurrent Pregnancy Loss. OGIJ 2017;7. [DOI: 10.15406/ogij.2017.07.00272] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
34 Ryu CS, Sakong JH, Ahn EH, Kim JO, Ko D, Kim JH, Lee WS, Kim NK. Association study of the three functional polymorphisms (TAS2R46G>A, OR4C16G>A, and OR4X1A>T) with recurrent pregnancy loss. Genes Genomics 2019;41:61-70. [PMID: 30203366 DOI: 10.1007/s13258-018-0738-5] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 3.8] [Reference Citation Analysis]
35 Quintero-Ronderos P, Laissue P. Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches. Reprod Sci 2020;27:1541-52. [PMID: 32430708 DOI: 10.1007/s43032-020-00187-6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
36 Normand EA, Alaimo JT, Van den Veyver IB. Exome and genome sequencing in reproductive medicine. Fertil Steril 2018;109:213-20. [PMID: 29395096 DOI: 10.1016/j.fertnstert.2017.12.010] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]