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For: Wojcik MH, Schwartz TS, Thiele KE, Paterson H, Stadelmaier R, Mullen TE, VanNoy GE, Genetti CA, Madden JA, Gubbels CS, Yu TW, Tan WH, Agrawal PB. Infant mortality: the contribution of genetic disorders. J Perinatol 2019;39:1611-9. [PMID: 31395954 DOI: 10.1038/s41372-019-0451-5] [Cited by in Crossref: 12] [Cited by in F6Publishing: 17] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Li M, Chien T, Liao K, Lai F. Using the Sankey diagram to visualize article features on the topics of whole-exome sequencing (WES) and whole-genome sequencing (WGS) since 2012: Bibliometric analysis. Medicine 2022;101:e30682. [DOI: 10.1097/md.0000000000030682] [Reference Citation Analysis]
2 Wojcik MH, Bresnahan M, Del Rosario MC, Ojeda MM, Kritzer A, Fraiman YS. Rare diseases, common barriers: disparities in pediatric clinical genetics outcomes. Pediatr Res 2022. [PMID: 35963884 DOI: 10.1038/s41390-022-02240-3] [Reference Citation Analysis]
3 Wojcik MH, D'Gama AM, Agrawal PB. A model to implement genomic medicine in the neonatal intensive care unit. J Perinatol 2022. [PMID: 35750755 DOI: 10.1038/s41372-022-01428-z] [Reference Citation Analysis]
4 Sanford Kobayashi EF, Dimmock DP. Better and faster is cheaper. Hum Mutat 2022. [PMID: 35723630 DOI: 10.1002/humu.24422] [Reference Citation Analysis]
5 Wojcik MH, Del Rosario MC, Agrawal PB. Perspectives of United States neonatologists on genetic testing practices. Genet Med 2022;24:1372-7. [PMID: 35304021 DOI: 10.1016/j.gim.2022.02.009] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Muniesa-Vargas A, Theil AF, Ribeiro-Silva C, Vermeulen W, Lans H. XPG: a multitasking genome caretaker. Cell Mol Life Sci 2022;79:166. [PMID: 35230528 DOI: 10.1007/s00018-022-04194-5] [Reference Citation Analysis]
7 Kotecha UH, Mistri M, Rayabarapu P, Shah P, Shah N. The diagnostic utility of exome-based carrier screening in families with a positive family history. Am J Med Genet A 2022. [PMID: 34997808 DOI: 10.1002/ajmg.a.62633] [Reference Citation Analysis]
8 Al-Hamed MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes. Hum Genet 2021. [PMID: 34853893 DOI: 10.1007/s00439-021-02406-9] [Reference Citation Analysis]
9 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] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 McKenzie-Sampson S, Baer RJ, Blebu BE, Karasek D, Oltman SP, Pantell MS, Rand L, Rogers EE, Torres JM, Jelliffe-Pawlowski LL, Scott KA, Chambers BD. Maternal nativity and risk of adverse perinatal outcomes among Black women residing in California, 2011-2017. J Perinatol 2021. [PMID: 34282261 DOI: 10.1038/s41372-021-01149-9] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
11 Owen MJ, Lenberg J, Feigenbaum A, Gold J, Chau K, Bezares-Orin Z, Ding Y, Chowdhury S, Kingsmore SF. Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency. Cold Spring Harb Mol Case Stud 2021;7:a006091. [PMID: 34117075 DOI: 10.1101/mcs.a006091] [Reference Citation Analysis]
12 Tolusso LK, Hazelton P, Wong B, Swarr DT. Beyond diagnostic yield: prenatal exome sequencing results in maternal, neonatal, and familial clinical management changes. Genet Med 2021;23:909-17. [PMID: 33442022 DOI: 10.1038/s41436-020-01067-9] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
13 Dimmock DP, Clark MM, Gaughran M, Cakici JA, Caylor SA, Clarke C, Feddock M, Chowdhury S, Salz L, Cheung C, Bird LM, Hobbs C, Wigby K, Farnaes L, Bloss CS, Kingsmore SF; RCIGM Investigators. An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm. Am J Hum Genet 2020;107:942-52. [PMID: 33157007 DOI: 10.1016/j.ajhg.2020.10.003] [Cited by in Crossref: 37] [Cited by in F6Publishing: 40] [Article Influence: 18.5] [Reference Citation Analysis]
14 Dempsey E, Pryce J, Thilaganathan B, Mansour S, Homfray T, Drury S. Diagnosis of fetal abnormalities using exome sequencing: translating research into practice. Ultrasound Obstet Gynecol 2020;56:779. [PMID: 31875334 DOI: 10.1002/uog.21959] [Reference Citation Analysis]
15 Kingsmore SF, Henderson A, Owen MJ, Clark MM, Hansen C, Dimmock D, Chambers CD, Jeliffe-Pawlowski LL, Hobbs C. Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing. NPJ Genom Med 2020;5:49. [PMID: 33154820 DOI: 10.1038/s41525-020-00155-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
16 Wojcik MH, Agrawal PB. Deciphering congenital anomalies for the next generation. Cold Spring Harb Mol Case Stud 2020;6:a005504. [PMID: 32826208 DOI: 10.1101/mcs.a005504] [Reference Citation Analysis]
17 de Castro MJ, González-Vioque E, Barbosa-Gouveia S, Salguero E, Rite S, López-Suárez O, Pérez-Muñuzuri A, Couce ML. Rapid Phenotype-Driven Gene Sequencing with the NeoSeq Panel: A Diagnostic Tool for Critically Ill Newborns with Suspected Genetic Disease. J Clin Med 2020;9:E2362. [PMID: 32718099 DOI: 10.3390/jcm9082362] [Cited by in Crossref: 1] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]