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1 April 1997
THE GILBERT SYNDROME ALLELE: A RISK FACTOR FOR JAUNDICE IN G-6-PD DEFICIENT AND NORMAL NEONATES. † 928
Pediatric Research 41 , 157–157

Rights & permissionsfor article THE GILBERT SYNDROME ALLELE: A RISK FACTOR FOR JAUNDICE IN G-6-PD DEFICIENT AND NORMAL NEONATES. † 928 . Opens in a new window.
Amendments and Corrections | 19 December 2019
Correction: Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral
- Sari Lieberman
- , Ariela Tomer
- , Avi Ben-Chetrit
- , Oded Olsha
- , Shalom Strano
- , Rachel Beeri
- , Sivan Koka
- , Hila Fridman
- , Karen Djemal
- , Itzhak Glick
- , Todd Zalut
- , Shlomo Segev
- , Miri Sklair
- , Bella Kaufman
- , Amnon Lahad
- , Aviad Raz
- & Ephrat Levy-Lahad
Genetics in Medicine 22 , 672–672

Rights & permissionsfor article Correction: Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral . Opens in a new window.
1 June 2008
Response to ACMG guideline: Carrier screening in individuals of Ashkenazi Jewish decent
Genetics in Medicine 10 , 462–462

Rights & permissionsfor article Response to ACMG guideline: Carrier screening in individuals of Ashkenazi Jewish decent . Opens in a new window.
17 August 2009
Population-based BRCA1/BRCA2 screening in Ashkenazi Jews: A call for evidence
- Ephrat Levy-Lahad
Genetics in Medicine 11 , 620–621

Rights & permissionsfor article Population-based BRCA1/BRCA2 screening in Ashkenazi Jews: A call for evidence . Opens in a new window.
Research | 1 January 2001
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
- Robert S. Wildin
- , Fred Ramsdell
- , Jane Peake
- , Francesca Faravelli
- , Jean-Laurent Casanova
- , Neil Buist
- , Ephrat Levy-Lahad
- , Massimo Mazzella
- , Olivier Goulet
- , Lucia Perroni
- , Franca Dagna Bricarelli
- , Geoffrey Byrne
- , Mark McEuen
- , Sean Proll
- , Mark Appleby
- & Mary E. Brunkow
Nature Genetics 27 , 18–20

Rights & permissionsfor article X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy . Opens in a new window.
1 January 2008
(TA)_n UDP-Glucuronosyltransferase 1A1 Promoter Polymorphism in Nigerian Neonates
- Michael Kaplan
- , Tina Slusher
- , Paul Renbaum
- , Dominic F Essiet
- , Sunday Pam
- , Ephrat Levy-Lahad
- & Cathy Hammerman
Pediatric Research 63 , 109–111

Rights & permissionsfor article (TA)n UDP-Glucuronosyltransferase 1A1 Promoter Polymorphism in Nigerian Neonates . Opens in a new window.
News and Views | 1 May 2010
Fanconi anemia and breast cancer susceptibility meet again
- Ephrat Levy-Lahad
Nature Genetics 42 , 368–369

Rights & permissionsfor article Fanconi anemia and breast cancer susceptibility meet again . Opens in a new window.
Research | 17 October 2019
Preconception carrier screening yield: effect of variants of unknown significance in partners of carriers with clinically significant variants
Genetics in Medicine 22 , 646–653

Rights & permissionsfor article Preconception carrier screening yield: effect of variants of unknown significance in partners of carriers with clinically significant variants . Opens in a new window.
Research | 11 April 2019
Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delay
European Journal of Human Genetics 27 , 1315–1319

Rights & permissionsfor article Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delay . Opens in a new window.
Research | 29 October 2018 | Open
Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation
- David A. Zeevi
- , Fouad Zahdeh
- , Yehuda Kling
- , Tzvia Rosen
- , Paul Renbaum
- , Raphael Ron-El
- , Talia Eldar-Geva
- , Hananel E. G. Holzer
- , Ephrat Levy-Lahad
- & Gheona Altarescu
Scientific Reports 8 , 1–9

Rights & permissionsfor article Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation . Opens in a new window.
Research | 15 February 2018 | Open
Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices
npj Genomic Medicine 3 , 1–8

Rights & permissionsfor article Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices . Opens in a new window.
Research | 29 March 2018
Familial communication and cascade testing among relatives of BRCA population screening participants
- Sari Lieberman
- , Amnon Lahad
- , Ariela Tomer
- , Sivan Koka
- , Malka BenUziyahu
- , Aviad Raz
- & Ephrat Levy-Lahad
Genetics in Medicine 20 , 1446–1454

Rights & permissionsfor article Familial communication and cascade testing among relatives of BRCA population screening participants . Opens in a new window.
1 December 2016
Population screening for BRCA1/BRCA2 mutations: lessons from qualitative analysis of the screening experience
- Sari Lieberman
- , Amnon Lahad
- , Ariela Tomer
- , Carmit Cohen
- , Ephrat Levy-Lahad
- & Aviad Raz
Genetics in Medicine 19 , 628–634

Rights & permissionsfor article Population screening for BRCA1/BRCA2 mutations: lessons from qualitative analysis of the screening experience . Opens in a new window.
8 December 2016
Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral
- Sari Lieberman
- , Ariela Tomer
- , Avi Ben-Chetrit
- , Oded Olsha
- , Shalom Strano
- , Rachel Beeri
- , Sivan Koka
- , Hila Fridman
- , Karen Djemal
- , Itzhak Glick
- , Todd Zalut
- , Shlomo Segev
- , Miri Sklair
- , Bella Kaufman
- , Amnon Lahad
- , Aviad Raz
- & Ephrat Levy-Lahad
Genetics in Medicine 19 , 754–762

Rights & permissionsfor article Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral . Opens in a new window.
1 June 2007
(TA)_n UGT 1A1 Promoter Polymorphism: A Crucial Factor in the Pathophysiology of Jaundice in G-6-PD Deficient Neonates
Pediatric Research 61 , 727–731

Rights & permissionsfor article (TA)n UGT 1A1 Promoter Polymorphism: A Crucial Factor in the Pathophysiology of Jaundice in G-6-PD Deficient Neonates . Opens in a new window.
1 August 2010
Collaborative genomics for human health and cooperation in the Mediterranean region
Nature Genetics 42 , 641–645

Rights & permissionsfor article Collaborative genomics for human health and cooperation in the Mediterranean region . Opens in a new window.
5 April 2012
BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening
Genetics in Medicine 14 , 688–694

Rights & permissionsfor article BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening . Opens in a new window.
Research | 1 October 2001
Differing Pathogenesis of Perinatal Bilirubinemia in Glucose-6-Phosphate Dehydrogenase-Deficient Versus-Normal Neonates
Pediatric Research 50 , 532–537

Rights & permissionsfor article Differing Pathogenesis of Perinatal Bilirubinemia in Glucose-6-Phosphate Dehydrogenase-Deficient Versus-Normal Neonates . Opens in a new window.
15 January 2010
Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: A change of concept required
Genetics in Medicine 12 , 122–125

Rights & permissionsfor article Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: A change of concept required . Opens in a new window.
Research | 19 November 2018
Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy
- Daniel Backenroth
- , Fouad Zahdeh
- , Yehuda Kling
- , Aharon Peretz
- , Tzvia Rosen
- , Dina Kort
- , Sharon Zeligson
- , Tal Dror
- , Sophie Kirshberg
- , Efrat Burak
- , Reeval Segel
- , Ephrat Levy-Lahad
- , David Zangen
- , Gheona Altarescu
- , Shai Carmi
- & David A. Zeevi
Genetics in Medicine 21 , 1390–1399

Rights & permissionsfor article Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy . Opens in a new window.
Research | 26 July 2018 | Open
Vrk1 partial Knockdown in Mice Results in Reduced Brain Weight and Mild Motor Dysfunction, and Indicates Neuronal VRK1 Target Pathways
Scientific Reports 8 , 1–11

Rights & permissionsfor article Vrk1 partial Knockdown in Mice Results in Reduced Brain Weight and Mild Motor Dysfunction, and Indicates Neuronal VRK1 Target Pathways . Opens in a new window.
Research | 12 June 2015 | Open
VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle
Scientific Reports 5 , 1–18

Rights & permissionsfor article VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle . Opens in a new window.

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THE GILBERT SYNDROME ALLELE: A RISK FACTOR FOR JAUNDICE IN G-6-PD DEFICIENT AND NORMAL NEONATES. † 928

Correction: Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral

Response to ACMG guideline: Carrier screening in individuals of Ashkenazi Jewish decent

Population-based BRCA1/BRCA2 screening in Ashkenazi Jews: A call for evidence

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

(TA)_n UDP-Glucuronosyltransferase 1A1 Promoter Polymorphism in Nigerian Neonates

Fanconi anemia and breast cancer susceptibility meet again

Preconception carrier screening yield: effect of variants of unknown significance in partners of carriers with clinically significant variants

Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delay

Noninvasive paternal exclusion testing for cystic fibrosis in the first five to eight weeks of gestation

Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices

Familial communication and cascade testing among relatives of BRCA population screening participants

Population screening for BRCA1/BRCA2 mutations: lessons from qualitative analysis of the screening experience

Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referral

(TA)_n UGT 1A1 Promoter Polymorphism: A Crucial Factor in the Pathophysiology of Jaundice in G-6-PD Deficient Neonates

Collaborative genomics for human health and cooperation in the Mediterranean region

BRCA genetic testing of individuals from families with low prevalence of cancer: experiences of carriers and implications for population screening

Differing Pathogenesis of Perinatal Bilirubinemia in Glucose-6-Phosphate Dehydrogenase-Deficient Versus-Normal Neonates

Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: A change of concept required

Haploseek: a 24-hour all-in-one method for preimplantation genetic diagnosis (PGD) of monogenic disease and aneuploidy

Vrk1 partial Knockdown in Mice Results in Reduced Brain Weight and Mild Motor Dysfunction, and Indicates Neuronal VRK1 Target Pathways

VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle

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