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For: Filges I, Friedman JM. Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypes. Prenat Diagn 2015;35:1005-9. [PMID: 25046514 DOI: 10.1002/pd.4464] [Cited by in Crossref: 62] [Cited by in F6Publishing: 68] [Article Influence: 6.9] [Reference Citation Analysis]
Number Citing Articles
1 Filges I, Jünemann S, Viehweger E, Tercanli S. Fetal arthrogryposis-what do we tell the prospective parents? Prenat Diagn 2023. [PMID: 36588183 DOI: 10.1002/pd.6299] [Reference Citation Analysis]
2 Cacheiro P, Westerberg CH, Mager J, Dickinson ME, Nutter LMJ, Muñoz-Fuentes V, Hsu CW, Van den Veyver IB, Flenniken AM, McKerlie C, Murray SA, Teboul L, Heaney JD, Lloyd KCK, Lanoue L, Braun RE, White JK, Creighton AK, Laurin V, Guo R, Qu D, Wells S, Cleak J, Bunton-Stasyshyn R, Stewart M, Harrisson J, Mason J, Haseli Mashhadi H, Parkinson H, Mallon AM, Smedley D; International Mouse Phenotyping Consortium., Genomics England Research Consortium. Mendelian gene identification through mouse embryo viability screening. Genome Med 2022;14:119. [PMID: 36229886 DOI: 10.1186/s13073-022-01118-7] [Reference Citation Analysis]
3 Dhombres F, Morgan P, Chaudhari BP, Filges I, Sparks TN, Lapunzina P, Roscioli T, Agarwal U, Aggarwal S, Beneteau C, Cacheiro P, Carmody LC, Collardeau-Frachon S, Dempsey EA, Dufke A, Duyzend MH, El Ghosh M, Giordano JL, Glad R, Grinfelde I, Iliescu DG, Ladewig MS, Munoz-Torres MC, Pollazzon M, Radio FC, Rodo C, Silva RG, Smedley D, Sundaramurthi JC, Toro S, Valenzuela I, Vasilevsky NA, Wapner RJ, Zemet R, Haendel MA, Robinson PN. Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology. Am J Med Genet C Semin Med Genet 2022;190:231-42. [PMID: 35872606 DOI: 10.1002/ajmg.c.31989] [Reference Citation Analysis]
4 Yang Y, Wang M, Wang H. Prenatal trio-based whole exome sequencing in fetuses with abnormalities of the skeletal system. Mol Genet Genomics 2022. [PMID: 35583673 DOI: 10.1007/s00438-022-01899-x] [Reference Citation Analysis]
5 Buonaiuto S, Biase ID, Aleotti V, Ravaei A, Marino A, Damaggio G, Chierici M, Pulijala M, D'Ambrosio P, Esposito G, Ayub Q, Furlanello C, Greco P, Capalbo A, Rubini M, Biase SD, Colonna V. Prioritization of putatively detrimental variants in euploid miscarriages. Sci Rep 2022;12:1997. [PMID: 35132093 DOI: 10.1038/s41598-022-05737-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Cacheiro P, Westerberg CH, Mager J, Dickinson ME, Nutter LM, Muñoz-fuentes V, Hsu C, Van den Veyver IB, Flenniken AM, Mckerlie C, Murray SA, Teboul L, Heaney JD, Lloyd KCK, Lanoue L, Braun RE, White JK, Creighton AK, Laurin V, Guo R, Qu D, Wells S, Cleak J, Bunton-stasyshyn R, Stewart M, Harrisson J, Mason J, Mashhadi HH, Parkinson H, Mallon A, Smedley D, International Mouse Phenotyping Consortium, Genomics England Research Consortium. Mendelian gene identification through mouse embryo viability screening.. [DOI: 10.1101/2022.01.07.22268899] [Reference Citation Analysis]
7 Filges I, Miny P, Holzgreve W, Tercanli S. How genomics is changing the practice of prenatal testing. J Perinat Med 2021. [PMID: 34214293 DOI: 10.1515/jpm-2021-0220] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
8 Aggarwal S. Role of whole exome sequencing for unidentified genetic syndromes. Curr Opin Obstet Gynecol 2021;33:112-22. [PMID: 33620889 DOI: 10.1097/GCO.0000000000000688] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
9 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] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 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] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Guadagnolo D, Mastromoro G, Di Palma F, Pizzuti A, Marchionni E. Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives-A Systematic Review. Diagnostics (Basel) 2021;11:224. [PMID: 33540854 DOI: 10.3390/diagnostics11020224] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 4.5] [Reference Citation Analysis]
12 Buonaiuto S, Di Biase I, Aleotti V, Ravaei A, Marino AD, Damaggio G, Chierici M, Pulijala M, D’ambrosio P, Esposito G, Ayub Q, Furlanello C, Greco P, Capalbo A, Rubini M, Biase SD, Colonna V. Prioritization of putatively detrimental variants in euploid miscarriages.. [DOI: 10.1101/2021.01.02.20248961] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Diderich KEM, Romijn K, Joosten M, Govaerts LCP, Polak M, Bruggenwirth HT, Wilke M, van Slegtenhorst MA, van Bever Y, Brooks AS, Mancini GMS, van de Laar IMBH, Kromosoeto JNR, Knapen MFCM, Go ATJI, Van Opstal D, Hoefsloot LH, Galjaard RH, Srebniak MI. The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies. Acta Obstet Gynecol Scand 2021;100:1106-15. [PMID: 33249554 DOI: 10.1111/aogs.14053] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
14 Lefebvre M, Bruel AL, Tisserant E, Bourgon N, Duffourd Y, Collardeau-Frachon S, Attie-Bitach T, Kuentz P, Assoum M, Schaefer E, El Chehadeh S, Antal MC, Kremer V, Girard-Lemaitre F, Mandel JL, Lehalle D, Nambot S, Jean-Marçais N, Houcinat N, Moutton S, Marle N, Lambert L, Jonveaux P, Foliguet B, Mazutti JP, Gaillard D, Alanio E, Poirisier C, Lebre AS, Aubert-Lenoir M, Arbez-Gindre F, Odent S, Quélin C, Loget P, Fradin M, Willems M, Bigi N, Perez MJ, Blesson S, Francannet C, Beaufrere AM, Patrier-Sallebert S, Guerrot AM, Goldenberg A, Brehin AC, Lespinasse J, Touraine R, Capri Y, Saint-Frison MH, Laurent N, Philippe C, Tran Mau-Them F, Thevenon J, Faivre L, Thauvin-Robinet C, Vitobello A. Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations. J Med Genet 2021;58:400-13. [PMID: 32732226 DOI: 10.1136/jmedgenet-2020-106867] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
15 Zhao C, Chai H, Zhou Q, Wen J, Reddy UM, Kastury R, Jiang Y, Mak W, Bale AE, Zhang H, Li P. Whole-exome sequencing analysis on products of conception: A cohort study to evaluate clinical utility and genetic etiology for pregnancy loss.. [DOI: 10.1101/2020.07.19.20150144] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
16 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: 9] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
17 Kalantari S, Filges I. 'Kinesinopathies': emerging role of the kinesin family member genes in birth defects. J Med Genet 2020;57:797-807. [PMID: 32430361 DOI: 10.1136/jmedgenet-2019-106769] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
18 Wojcik MH, Reimers R, Poorvu T, Agrawal PB. Genetic diagnosis in the fetus. J Perinatol 2020;40:997-1006. [PMID: 32094481 DOI: 10.1038/s41372-020-0627-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
19 Rinaldi B, Race V, Corveleyn A, Van Hoof E, Bauters M, Van Den Bogaert K, Denayer E, de Ravel T, Legius E, Baldewijns M, Aertsen M, Lewi L, De Catte L, Breckpot J, Devriendt K. Next-generation sequencing in prenatal setting: Some examples of unexpected variant association. Eur J Med Genet 2020;63:103875. [PMID: 32058062 DOI: 10.1016/j.ejmg.2020.103875] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
20 Vora NL, Gilmore K, Brandt A, Gustafson C, Strande N, Ramkissoon L, Hardisty E, Foreman AKM, Wilhelmsen K, Owen P, Weck KE, Berg JS, Powell CM, Powell BC. An approach to integrating exome sequencing for fetal structural anomalies into clinical practice. Genet Med 2020;22:954-61. [PMID: 31974414 DOI: 10.1038/s41436-020-0750-4] [Cited by in Crossref: 29] [Cited by in F6Publishing: 32] [Article Influence: 9.7] [Reference Citation Analysis]
21 Hollenbach SJ, Westen EA, Thornburg LL. Obstetric Management in Life-Limiting Fetal Conditions. Perinatal Palliative Care 2020. [DOI: 10.1007/978-3-030-34751-2_5] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
22 Aggarwal S, Vineeth VS, Das Bhowmik A, Tandon A, Kulkarni A, Narayanan DL, Bhattacherjee A, Dalal A. Exome sequencing for perinatal phenotypes: The significance of deep phenotyping. Prenat Diagn 2020;40:260-73. [PMID: 31742715 DOI: 10.1002/pd.5616] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
23 Sabbagh R, Van den Veyver IB. The current and future impact of genome-wide sequencing on fetal precision medicine. Hum Genet 2020;139:1121-30. [PMID: 31754893 DOI: 10.1007/s00439-019-02088-4] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.5] [Reference Citation Analysis]
24 Guo W, Lai Y, Yan Z, Wang Y, Nie Y, Guan S, Kuo Y, Zhang W, Zhu X, Peng M, Zhi X, Wei Y, Yan L, Qiao J. Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations. Hum Mutat 2020;41:432-48. [PMID: 31680349 DOI: 10.1002/humu.23935] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
25 Abou Tayoun A, Mason-Suares H. Considerations for whole exome sequencing unique to prenatal care. Hum Genet 2020;139:1149-59. [PMID: 31701237 DOI: 10.1007/s00439-019-02085-7] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 2.8] [Reference Citation Analysis]
26 Lamont RE, Xi Y, Popko C, Lazier J, Bernier FP, Lauzon JL, Innes AM, Parboosingh JS, Thomas MA. Next-Generation Sequencing Using a Cardiac Gene Panel in Prenatally Diagnosed Cardiac Anomalies. J Obstet Gynaecol Can 2018;40:1417-23. [PMID: 30473118 DOI: 10.1016/j.jogc.2018.02.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
27 Fallet-Bianco C, De Bie I, Désilets V, Oligny LL. No. 365-Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities with Normal Chromosome Analysis. J Obstet Gynaecol Can 2018;40:1358-1366.e5. [PMID: 30390949 DOI: 10.1016/j.jogc.2018.05.017] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
28 Filges I, Tercanli S, Hall JG. Fetal arthrogryposis: Challenges and perspectives for prenatal detection and management. Am J Med Genet C Semin Med Genet 2019;181:327-36. [PMID: 31318155 DOI: 10.1002/ajmg.c.31723] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [Reference Citation Analysis]
29 Ferretti L, Mellis R, Chitty LS. Update on the use of exome sequencing in the diagnosis of fetal abnormalities. Eur J Med Genet 2019;62:103663. [PMID: 31085342 DOI: 10.1016/j.ejmg.2019.05.002] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 8.0] [Reference Citation Analysis]
30 Dawes R, Lek M, Cooper ST. Gene discovery informatics toolkit defines candidate genes for unexplained infertility and prenatal or infantile mortality. NPJ Genom Med 2019;4:8. [PMID: 30993004 DOI: 10.1038/s41525-019-0081-z] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [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: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
32 Meier N, Bruder E, Lapaire O, Hoesli I, Kang A, Hench J, Hoeller S, De Geyter J, Miny P, Heinimann K, Chaoui R, Tercanli S, Filges I. Exome sequencing of fetal anomaly syndromes: novel phenotype-genotype discoveries. Eur J Hum Genet 2019;27:730-7. [PMID: 30679815 DOI: 10.1038/s41431-018-0324-y] [Cited by in Crossref: 34] [Cited by in F6Publishing: 35] [Article Influence: 8.5] [Reference Citation Analysis]
33 Borrell A. A new comprehensive paradigm for prenatal diagnosis: seeing the forest through the trees. Ultrasound Obstet Gynecol 2018;52:563-8. [PMID: 29484739 DOI: 10.1002/uog.19035] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
34 Normand EA, Van den Veyver IB. Next-Generation Sequencing for Gene Panels and Clinical Exomes. Human Reproductive and Prenatal Genetics 2019. [DOI: 10.1016/b978-0-12-813570-9.00025-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
35 Van den Veyver IB. Exome and Genome Sequencing. Perinatal Genetics 2019. [DOI: 10.1016/b978-0-323-53094-1.00013-8] [Reference Citation Analysis]
36 Fallet-Bianco C, De Bie I, Désilets V, Oligny LL. N° 365 -Autopsies fœtales et périnatales en cas d'anomalies fœtales diagnostiquées avant la naissance avec une analyse chromosomique normale. J Obstet Gynaecol Can 2018;40:1367-1377.e6. [PMID: 30390950 DOI: 10.1016/j.jogc.2018.08.006] [Reference Citation Analysis]
37 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: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.6] [Reference Citation Analysis]
38 Miny P, Filges I, Tercanli S, Holzgreve W. Foetal Diagnosis. In: John Wiley & Sons Ltd, editor. eLS. Chichester: John Wiley & Sons, Ltd; 2001. pp. 1-7. [DOI: 10.1002/9780470015902.a0027053] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
39 Wojcik MH, Brodsky D, Stewart JE, Picker J. Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technology. J Perinatol 2018;38:1125-34. [PMID: 30076402 DOI: 10.1038/s41372-018-0187-7] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
40 Vora NL, Hui L. Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development. Genet Med 2018;20:791-9. [PMID: 30032162 DOI: 10.1038/s41436-018-0087-4] [Cited by in Crossref: 19] [Cited by in F6Publishing: 21] [Article Influence: 3.8] [Reference Citation Analysis]
41 Renga B. Non invasive prenatal diagnosis of fetal aneuploidy using cell free fetal DNA. European Journal of Obstetrics & Gynecology and Reproductive Biology 2018;225:5-8. [DOI: 10.1016/j.ejogrb.2018.03.033] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 4.8] [Reference Citation Analysis]
42 Roessler E, Hu P, Muenke M. Holoprosencephaly in the genomics era. Am J Med Genet C Semin Med Genet 2018;178:165-74. [PMID: 29770992 DOI: 10.1002/ajmg.c.31615] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 7.0] [Reference Citation Analysis]
43 Pinar MH, Gibbins K, He M, Kostadinov S, Silver R. Early Pregnancy Losses: Review of Nomenclature, Histopathology, and Possible Etiologies. Fetal Pediatr Pathol 2018;37:191-209. [PMID: 29737906 DOI: 10.1080/15513815.2018.1455775] [Cited by in Crossref: 29] [Cited by in F6Publishing: 23] [Article Influence: 5.8] [Reference Citation Analysis]
44 Aggarwal S, Tandon A, Das Bhowmik A, Safarulla JMNJ, Dalal A. A Dysmorphology Based Systematic Approach Toward Perinatal Genetic Diagnosis in a Fetal Autopsy Series. Fetal Pediatr Pathol 2018;37:49-68. [PMID: 29336636 DOI: 10.1080/15513815.2017.1397070] [Reference Citation Analysis]
45 Hayward J, Chitty LS. Beyond screening for chromosomal abnormalities: Advances in non-invasive diagnosis of single gene disorders and fetal exome sequencing. Semin Fetal Neonatal Med 2018;23:94-101. [PMID: 29305293 DOI: 10.1016/j.siny.2017.12.002] [Cited by in Crossref: 44] [Cited by in F6Publishing: 44] [Article Influence: 8.8] [Reference Citation Analysis]
46 Quinlan-jones E, Kilby MD. Exome Sequencing in the Evaluation of the Fetus With Structural Anomalies. Noninvasive Prenatal Testing (NIPT) 2018. [DOI: 10.1016/b978-0-12-814189-2.00017-7] [Reference Citation Analysis]
47 Hardisty EE, Vora N, Korpi-Steiner N. Unveiling Fetal Development by Use of "Omics". Clin Chem 2017;63:1549. [PMID: 32100829 DOI: 10.1373/clinchem.2017.274910] [Reference Citation Analysis]
48 Shim SH, Kim JY, Sung SR, Park JE, Shin YJ, Shim SH, Cha DH. Prenatally diagnosed TTN mutation with repeated bilateral club foot by whole exome sequencing. BioChip J 2017;11:240-5. [DOI: 10.1007/s13206-017-1309-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
49 Feiglin A, Allen BK, Kohane IS, Kong SW. Comprehensive Analysis of Tissue-wide Gene Expression and Phenotype Data Reveals Tissues Affected in Rare Genetic Disorders. Cell Syst 2017;5:140-148.e2. [PMID: 28822752 DOI: 10.1016/j.cels.2017.06.016] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 2.3] [Reference Citation Analysis]
50 Best S, Wou K, Vora N, Van der Veyver IB, Wapner R, Chitty LS. Promises, pitfalls and practicalities of prenatal whole exome sequencing. Prenat Diagn 2018;38:10-9. [PMID: 28654730 DOI: 10.1002/pd.5102] [Cited by in Crossref: 190] [Cited by in F6Publishing: 205] [Article Influence: 31.7] [Reference Citation Analysis]
51 Altmüller J, Motameny S, Becker C, Thiele H, Chatterjee S, Wollnik B, Nürnberg P. A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product. Biol Chem 2016;397:791-801. [PMID: 27021259 DOI: 10.1515/hsz-2015-0300] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 2.2] [Reference Citation Analysis]
52 Meier N, Bruder E, Filges I. A novel homozygous splice‐site mutation in RYR1 causes fetal hydrops and affects skeletal and smooth muscle development. Prenat Diagn 2017;37:720-4. [DOI: 10.1002/pd.5073] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
53 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] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
54 Filges I. Gene Discovery in Lethal Foetal Disorders. eLS 2017. [DOI: 10.1002/9780470015902.a0026660] [Reference Citation Analysis]
55 Goldstein M, Svirsky R, Reches A, Yaron Y. Does the number of previous miscarriages influence the incidence of chromosomal aberrations in spontaneous pregnancy loss? J Matern Fetal Neonatal Med 2017;30:2956-60. [PMID: 27923289 DOI: 10.1080/14767058.2016.1269317] [Cited by in Crossref: 19] [Cited by in F6Publishing: 16] [Article Influence: 3.2] [Reference Citation Analysis]
56 Rajcan-separovic E. Candidate Genes for Pregnancy Loss. Early Pregnancy 2017. [DOI: 10.1017/9781139976787.011] [Reference Citation Analysis]
57 Van den Veyver IB. Recent advances in prenatal genetic screening and testing. F1000Res 2016;5:2591. [PMID: 27853526 DOI: 10.12688/f1000research.9215.1] [Cited by in Crossref: 42] [Cited by in F6Publishing: 44] [Article Influence: 6.0] [Reference Citation Analysis]
58 Shaheen R, Hashem A, Abdel-Salam GM, Al-Fadhli F, Ewida N, Alkuraya FS. Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans. Hum Genet 2016;135:1191-7. [PMID: 27503289 DOI: 10.1007/s00439-016-1722-2] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 3.6] [Reference Citation Analysis]
59 Pangalos C. Approches génomiques prénatales pour la détection des mutations géniques associées à des maladies génétiques liées à des anomalies échographiques. Bulletin de l'Académie Nationale de Médecine 2016;200:1179-1189. [DOI: 10.1016/s0001-4079(19)30638-7] [Reference Citation Analysis]
60 Pangalos C, Hagnefelt B, Lilakos K, Konialis C. First applications of a targeted exome sequencing approach in fetuses with ultrasound abnormalities reveals an important fraction of cases with associated gene defects. PeerJ 2016;4:e1955. [PMID: 27168972 DOI: 10.7717/peerj.1955] [Cited by in Crossref: 51] [Cited by in F6Publishing: 55] [Article Influence: 7.3] [Reference Citation Analysis]
61 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: 50] [Cited by in F6Publishing: 53] [Article Influence: 7.1] [Reference Citation Analysis]
62 Chitty LS, Friedman JM, Langlois S. Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus? Prenat Diagn 2016;36:15-9. [PMID: 26525746 DOI: 10.1002/pd.4718] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 1.8] [Reference Citation Analysis]
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