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Cited by in F6Publishing

For:	Mis EK, Al-Ali S, Ji W, Spencer-Manzon M, Konstantino M, Khokha MK, Jeffries L, Lakhani SA. The latest FADS: Functional analysis of GLDN patient variants and classification of GLDN-associated AMC as a type of viable fetal akinesia deformation sequence. Am J Med Genet A 2020;182:2291-6. [PMID: 32812332 DOI: 10.1002/ajmg.a.61783] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]

For:

Mis EK, Al-Ali S, Ji W, Spencer-Manzon M, Konstantino M, Khokha MK, Jeffries L, Lakhani SA. The latest FADS: Functional analysis of GLDN patient variants and classification of GLDN-associated AMC as a type of viable fetal akinesia deformation sequence. Am J Med Genet A 2020;182:2291-6. [PMID: 32812332 DOI: 10.1002/ajmg.a.61783] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]

Number	Citing Articles
1	Al-Ali S, Jeffries L, Faustino EVS, Ji W, Mis E, Konstantino M, Zerillo C, Jiang YH, Spencer-Manzon M, Bale A, Zhang H, McGlynn J, McGrath JM, Tremblay T, Brodsky NN, Lucas CL, Pierce R, Deniz E, Khokha MK, Lakhani SA. A retrospective cohort analysis of the Yale pediatric genomics discovery program. Am J Med Genet A 2022;188:2869-78. [PMID: 35899841 DOI: 10.1002/ajmg.a.62918] [Reference Citation Analysis]
2	Potrony M, Borrell A, Masoller N, Nadal A, Rodriguez-carunchio L, Saez de Gordoa Elizalde K, Quesada-espinosa JF, Villanueva-cañas JL, Pauta M, Jodar M, Madrigal I, Badenas C, Alvarez-mora MI, Rodriguez-revenga L. Lethal Congenital Contracture Syndrome 11: A Case Report and Literature Review. JCM 2022;11:3570. [DOI: 10.3390/jcm11133570] [Reference Citation Analysis]
3	Eurich B, Nitsche C, Lau M, Hanker B, Spiegler J, Stichtenoth G. Progressive Respiratory Insufficiency in a Teenager with Diaphragmatic Hypomotility Due to a Novel Combination of Gliomedin Gene Variants. Children 2022;9:797. [DOI: 10.3390/children9060797] [Reference Citation Analysis]
4	Hall JG. Deformations associated with arthrogryposis. Am J Med Genet A 2021;185:2676-82. [PMID: 33683011 DOI: 10.1002/ajmg.a.62151] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]