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	1	Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies Enthalten in European journal of human genetics 23.12.2022: 1-9
	2	Barriers and facilitators for the implementation of patient-centered care in cardiogenetics: a Delphi study among ERN GUARD-heart members Enthalten in European journal of human genetics 21.12.2022: 1-10
	3	Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ Enthalten in European journal of human genetics 19.12.2022: 1
	4	Panel testing for the molecular genetic diagnosis of congenital hypogonadotropic hypogonadism – a clinical perspective Enthalten in European journal of human genetics 15.12.2022: 1-8
	5	The implementation of large-scale genomic screening or diagnostic programmes: A rapid evidence review Enthalten in European journal of human genetics 14.12.2022: 1-14
	6	Non-invasive prenatal testing in Germany: a unique ethical and policy landscape Enthalten in European journal of human genetics 12.12.2022: 1-6
	7	Experiences of pregnant women with genome-wide non-invasive prenatal testing in a national screening program Enthalten in European journal of human genetics 9.12.2022: 1-7
	8	Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye Enthalten in European journal of human genetics 2.12.2022: 1
	9	ARHGAP35 is a novel factor disrupted in human developmental eye phenotypes Enthalten in European journal of human genetics 1.12.2022: 1-5
	10	Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ Enthalten in European journal of human genetics 1.12.2022: 1-3

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