Concepedia

Author

Lena Sagi‐Dain

Carmel Medical CenterORCID

Also Known As

L Dain, L Sagi-Dain, L Sagi‐Dain, L. Dain, L. Sagi-Dain, L. Sagi‐Dain, Lena DAIN, Lena Dain, Lena Sagi Dain, Lena Sagi-Dain

175

Publications

2.2K

Citations

24

H-Index

77

Concepts

All Affiliations

Carmel Medical CenterTechnion – Israel Institute of TechnologyRabin Medical CenterTel Aviv UniversityIsrael Ministry of Health
LS

About

Lena Sagi‐Dain is an author at Carmel Medical Center specializing in medicine, public health, and obstetrics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

14

17

628

2

Public Health

8

8

241

3

Anatomy

1

1

23

4

Biology

1

1

17

5

Biomedical Engineering

1

1

65

Lena Sagi‐Dain

×

36

Publications

1.2K

Citations

20

H-Index

YearCitations

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants

Jennifer J. Johnston, Jasper J. van der Smagt, Jill A. Rosenfeld,

Genetics in Medicine

2018

211

Anti-cyclic citrullinated protein antibodies as a predictor of response to anti-tumor necrosis factor-alpha therapy in patients with rheumatoid arthritis.

Yolanda Braun‐Moscovici, Doron Markovits, Oren Zinder,

PubMed

2006

116

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

Lena Sagi‐Dain, Lital Cohen Vig, Sarit Kahana,

Genetics in Medicine

2019

66

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

Lena Sagi‐Dain, David Bider, Jacob Levron,

Fertility and Sterility

2013

65

<scp><i>EIF2AK2</i></scp> Missense Variants Associated with Early Onset Generalized Dystonia

Demy J.S. Kuipers, Wim Mandemakers, Chin‐Song Lu,

Annals of Neurology

2020

63

Early exploration of COVID-19 vaccination safety and effectiveness during pregnancy: interim descriptive data from a prospective observational study

Inna Bleicher, Einav Kadour‐Peero, Lena Sagi‐Dain,

Vaccine

2021

54

Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy

Marialetizia Motta, Lena Sagi‐Dain, Oliver H.F. Krumbach,

Human Molecular Genetics

2019

50

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

Amihood Singer, Lena Sagi‐Dain

Acta Obstetricia Et Gynecologica Scandinavica

2020

42

Biallelic <i>ADAM22</i> pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy

Marieke M van der Knoop, Reza Maroofian, Yuko Fukata,

Brain

2022

41

<i>KCNK9</i> imprinting syndrome—further delineation of a possible treatable disorder

John M. Graham, Neda Zadeh, Melissa Kelley,

American Journal of Medical Genetics Part A

2016

39

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