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Impact of a national genetic carrier‐screening program for reproductive purposes

Acta obstetricia et gynecologica Scandinavica, 2020-06, Vol.99 (6), p.802-808

2020

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Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review

Prenatal diagnosis, 2017-11, Vol.37 (11), p.1061-1066

2017

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The effect of paternal age on assisted reproduction outcome

Fertility and sterility, 2011, Vol.95 (1), p.1-8

2011

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The value of routine hemoglobin level evaluation following elective cesarean section: Is it worthwhile?

International journal of gynecology and obstetrics, 2024-08

2024

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What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?

Acta obstetricia et gynecologica Scandinavica, 2020-06, Vol.99 (6), p.757-764

2020

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Effect of paternal age on reproductive outcomes in oocyte donation model: a systematic review

Fertility and sterility, 2015-10, Vol.104 (4), p.857-865.e1

2015

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Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies

Genetics in medicine, 2019-11, Vol.21 (11), p.2462-2467

2019

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The impact of endometrial injury on reproductive outcomes: results of an updated meta‐analysis

Reproductive medicine and biology, 2020-10, Vol.19 (4), p.334-349

2020

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High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?

Genetics in medicine, 2020-07, Vol.22 (7), p.1276-1277

2020

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Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions

European journal of human genetics : EJHG, 2021-08, Vol.29 (8), p.1292-1300

2021

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Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a "virtual fetus" model-a pilot study

Prenatal diagnosis, 2024-04, Vol.44 (4), p.511-518

2024

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Numerous Confounders Affecting the Alleged Association Between Cesarean Deliveries Under General Anesthesia and Autism Spectrum Disorder

Journal of autism and developmental disorders, 2020-02, Vol.50 (2), p.688-690

2020

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Ten points to consider when providing genetic counseling for variants of incomplete penetrance and variable expressivity detected in a prenatal setting

Acta obstetricia et gynecologica Scandinavica, 2020-11, Vol.99 (11), p.1427-1429

2020

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The effect of opting-in versus opting-out forming on the rate of reported variants of questionable significance in prenatal microarray

International journal of gynecology and obstetrics, 2024-07

2024

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A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly

American journal of medical genetics. Part A, 2021-10, Vol.185 (10), p.3161-3166

2021

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Thin endometrium in donor oocyte recipients: enigma or obstacle for implantation?

Fertility and sterility, 2013-11, Vol.100 (5), p.1289-1295.e2

2013

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A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature

American journal of medical genetics. Part A, 2020-01, Vol.182 (1), p.205-212

2020

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The impact of intentional endometrial injury on reproductive outcomes: a systematic review and meta-analysis

Human reproduction update, 2019-01, Vol.25 (1), p.95-113

2019

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Combination of early pushing with extended second stage increases the rates of spontaneous vaginal deliveries, but might be associated with adverse maternal and neonatal outcomes

Archives of gynecology and obstetrics, 2022, Vol.305 (1), p.39-45

2022

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In women with spontaneous vaginal delivery, repair of perineal tears might be easier compared to episiotomy

International Urogynecology Journal, 2021-07, Vol.32 (7), p.1727-1732

2021

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Diagnostic yield and recognized barriers of an adult neurogenetics clinic

Journal of community genetics, 2021-10, Vol.12 (4), p.569-576

2021

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The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions–A new syndrome or still an enigma?

American journal of medical genetics. Part A, 2021-05, Vol.185 (5), p.1461-1467

2021

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Whole‐exome sequencing reveals a novel missense mutation in the MARS gene related to a rare Charcot‐Marie‐Tooth neuropathy type 2U

Journal of the peripheral nervous system, 2018-06, Vol.23 (2), p.138-142

2018

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Risk factors associated with accidental fetal skin lacerations during cesarean delivery

International journal of gynecology and obstetrics, 2023-01, Vol.160 (1), p.131-135

2023

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Impact of a national genetic carrier‐screening program for reproductive purposes

Risk for chromosomal aberrations in apparently isolated intrauterine growth restriction: A systematic review

The effect of paternal age on assisted reproduction outcome

The value of routine hemoglobin level evaluation following elective cesarean section: Is it worthwhile?

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?

Effect of paternal age on reproductive outcomes in oocyte donation model: a systematic review

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies

EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia

The impact of endometrial injury on reproductive outcomes: results of an updated meta‐analysis

High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?

Is it time to report carrier state for recessive disorders in every microarray analysis?-A pilot model based on hearing loss genes deletions

Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a "virtual fetus" model-a pilot study

Numerous Confounders Affecting the Alleged Association Between Cesarean Deliveries Under General Anesthesia and Autism Spectrum Disorder

Ten points to consider when providing genetic counseling for variants of incomplete penetrance and variable expressivity detected in a prenatal setting

The effect of opting-in versus opting-out forming on the rate of reported variants of questionable significance in prenatal microarray

A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly

Thin endometrium in donor oocyte recipients: enigma or obstacle for implantation?

A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature

The impact of intentional endometrial injury on reproductive outcomes: a systematic review and meta-analysis

Combination of early pushing with extended second stage increases the rates of spontaneous vaginal deliveries, but might be associated with adverse maternal and neonatal outcomes

In women with spontaneous vaginal delivery, repair of perineal tears might be easier compared to episiotomy

Diagnostic yield and recognized barriers of an adult neurogenetics clinic

The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions–A new syndrome or still an enigma?

Whole‐exome sequencing reveals a novel missense mutation in the MARS gene related to a rare Charcot‐Marie‐Tooth neuropathy type 2U

Risk factors associated with accidental fetal skin lacerations during cesarean delivery

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