Dina Marek‐Yagel

2.5k citations

26 papers · 507 indexed · h-index 12

Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders 4
Biochemistry top 10%
- Amino Acid Enzymes and Metabolism 3
Immunology
Nephrology
Molecular Biology
- Mitochondrial Function and Pathology 5
- RNA regulation and disease 2
- Congenital heart defects research 2
Physiology
- Lysosomal Storage Disorders Research 3
Genetics
- Genetics and Neurodevelopmental Disorders 3
Surgery
- Helicobacter pylori-related gastroenterology studies 2

Co-authors: Haike Reznik‐Wolf Shai Padeh Avi Livneh Elon Pras Yackov Berkun Mordechai Pras Yair Anikster Ortal Barel
Cited by: Clinical Biochemistry Biochemistry Immunology
Journals: Digestive Diseases and Sciences (1 paper)Human Mutation (1 paper)Human Genetics (2 papers)
Partner nations: Israel United States Netherlands

In The Last Decade

Dina Marek‐Yagel

24 papers receiving 501 citations

Peers

Countries citing papers authored by Dina Marek‐Yagel

Since Specialization

Citations

This map shows the geographic impact of Dina Marek‐Yagel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dina Marek‐Yagel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dina Marek‐Yagel more than expected).

Fields of papers citing papers by Dina Marek‐Yagel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dina Marek‐Yagel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dina Marek‐Yagel. The network helps show where Dina Marek‐Yagel may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Dina Marek‐Yagel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dina Marek‐Yagel Line = papers co-authored together Dina Marek‐Yagel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder European Journal of Human Genetics ·Asier Iturrate,Nurit Assia Batzir,Ranit Jaron,David Garcia-Valentin,Julián Nevado,Jair Tenorio,Pablo Lapunzina,K.‐R. Lee,Rotem Greenberg,Dvora Sassi,Sharon Aharoni,Alla Kuzminsky,Lina Basel‐Salmon,Naama Orenstein,Yakov Fellig,Shay Ben‐Shachar,Dina Marek‐Yagel,Víctor L. Ruiz‐Pérez	2025	0
2	Biallelic MED29 variants cause pontocerebellar hypoplasia with cataracts European Journal of Human Genetics ·Leo Arkush,Geeske M. van Woerden,Limor Ziv,Dina Marek‐Yagel,R Nunes da Fonseca,Esmee Brevé,Ortal Barel,Nechama Shalva,Alvit Veber,Yair Anikster,Dominique Ben-Ami Raichman,Banan Musallam,Shai Marcu,Andreea Nissenkorn,Hanna Mandel,Steven A. Kushner,Bruria Ben Zeev,Gali Heimer	2025	0
3	Biallelic PIGM Coding Variant Causes Intractable Epilepsy and Intellectual Disability Without Thrombotic Events Clinical Genetics ·Gali Heimer,Ben Pode‐Shakked,Dina Marek‐Yagel,Helly Vernitsky,Michal Tzadok,Ortal Barel,Eran Eyal,Bruria Ben Zeev,Gil Atzmon,Yair Anikster	2024	1
4	Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy Human Genetics ·Dina Marek‐Yagel,Emily Stenke,Ben Pode‐Shakked,Cara Dunne,Ellen Crushell,Anthea Bryce-Smith,Michael McDermott,Maureen J. O’Sullivan,Alvit Veber,Mansa Krishnamurthy,James M. Wells,Yair Anikster,Billy Bourke	2022	1
5	Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene Frontiers in Genetics ·Dina Marek‐Yagel,Shachar Abudi-Sinreich,Michal Macarov,Alvit Veber,Nechama Shalva,Amit M. Philosoph,Ben Pode‐Shakked,May Christine V. Malicdan,Yair Anikster	2022	2
6	Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly European Journal of Medical Genetics ·Lina Basel‐Salmon,Noa Ruhrman‐Shahar,Ortal Barel,Ofir Hagari,Dina Marek‐Yagel,Noy Azulai,Lily Bazak,Ran Svirsky,Haike Reznik‐Wolf,Gabriel Lidzbarsky,Mordechai Shohat	2021	7
7	Four patients with D-bifunctional protein (DBP) deficiency: Expanding the phenotypic spectrum of a highly variable disease Molecular Genetics and Metabolism Reports ·Yuval E. Landau,Gali Heimer,Ortal Barel,Nechama Shalva,Dina Marek‐Yagel,Alvit Veber,Elisheva Javasky,Aya Shilon,Andreea Nissenkorn,Bruria Ben‐Zeev,Yair Anikster	2020	13
8	A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds American Journal of Medical Genetics Part A ·Dina Marek‐Yagel,Yoav Bolkier,Ortal Barel,Amir Vardi,David Mishali,Uriel Katz,Yishay Salem,Shachar Abudi,Omri Nayshool,Nitzan Kol,Annick Raas‐Rothschild,Gideon Rechavi,Yair Anikster,Ben Pode‐Shakked	2020	3
9	Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature BMC Medical Genetics ·Ben Pode‐Shakked,Asaf Vivante,Ortal Barel,Shai Padeh,Dina Marek‐Yagel,Alvit Veber,Shachar Abudi,Aviva Eliyahu,Irit Tirosh,Shiri Shpilman,Shirlee Shril,Friedhelm Hildebrandt,Mordechai Shohat,Yair Anikster	2019	13
10	Genetic and Structural Analysis of a SKIV2L Mutation Causing Tricho-hepato-enteric Syndrome Digestive Diseases and Sciences ·Iddo Vardi,Ortal Barel,Michal Sperber,Michael Schvimer,M Nunberg,Michael Field,Jodie Ouahed,Dina Marek‐Yagel,Lael Werner,Yael Haberman,Avishay Lahad,Yair Anikster,Gideon Rechavi,Iris Barshack,Joshua McElwee,Joseph Maranville,Raz Somech,Scott B. Snapper,Batia Weiss,Dror S. Shouval	2018	8
11	Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin European Journal of Paediatric Neurology ·Gali Heimer,Eran Eyal,Xiaolin Zhu,Elizabeth K. Ruzzo,Dina Marek‐Yagel,Doron Sagiv,Yair Anikster,Haike Reznik‐Wolf,Eran Pras,Dikla Levi,Doron Lancet,Bruria Ben‐Zeev,Andreea Nissenkorn	2017	37
12	Congenital protein losing enteropathy: an inborn error of lipid metabolism due to DGAT1 mutations European Journal of Human Genetics ·Joshi Stephen,Thierry Vilboux,Yael Haberman,Hadass Pri‐Chen,Ben Pode‐Shakked,Sina Mazaheri,Dina Marek‐Yagel,Ortal Barel,Ayelet Di Segni,Eran Eyal,Goni Hout‐Siloni,Avishay Lahad,Tzippora Shalem,Gideon Rechavi,May Christine V. Malicdan,Batia Weiss,William A. Gahl,Yair Anikster	2016	34
13	Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy Clinical Genetics ·Ben Pode‐Shakked,Hila Barash,Limor Ziv,Karen W. Gripp,Elisabetta Flex,Ortal Barel,Karinne Spirandelli Carvalho,Mena Scavina,Giovanni Chillemi,Marcello Niceta,Eran Eyal,Nitzan Kol,Bruria Ben‐Zeev,Omer Bar‐Yosef,Dina Marek‐Yagel,Enrico Bertini,Angela L. Duker,Yair Anikster,Marco Tartaglia,Annick Raas‐Rothschild	2016	22
14	A novel mutation in the C7orf11 gene causes nonphotosensitive trichothiodystrophy in a multiplex highly consanguineous kindred European Journal of Medical Genetics ·Ben Pode‐Shakked,Dina Marek‐Yagel,Shoshana Greenberger,Naomi Pode‐Shakked,Elon Pras,Aviv Barzilai,Saeed Yassin,Yechezkel Sidi,Yair Anikster	2015	5
15	Glutaric Aciduria type I and acute renal failure — Coincidence or causality? Molecular Genetics and Metabolism Reports ·Ben Pode‐Shakked,Dina Marek‐Yagel,Marina Rubinshtein,Itai M. Pessach,Gideon Paret,Alexander Volkov,Yair Anikster,Danny Lotan	2014	7
16	Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia Human Genetics ·Ifat Bar-Joseph,Elon Pras,Haike Reznik‐Wolf,Dina Marek‐Yagel,Almogit Abu-Horvitz,Maya Dushnitzky,Nurit Goldstein,Shlomit Rienstein,Michal Dekel,Ben Pode‐Shakked,J Zlotnik,Anelia Benarrosh,Philippe Gillery,N Höfliger,Christiane Auray‐Blais,Roselyne Garnotel,Yair Anikster	2012	18
17	X inactivation testing for identifying a non-syndromic X-linked mental retardation gene Journal of Applied Genetics ·Hagith Yonath,Dina Marek‐Yagel,Haike Resnik‐Wolf,Almogit Abu-Horvitz,Hagit Baris,Mordechai Shohat,Moshe Frydman,Elon Pras	2011	4
18	Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean Fever Arthritis Care & Research ·Dina Marek‐Yagel,Yackov Berkun,Shai Padeh,Merav Lidar,Yael Shinar,Ifat Bar-Joseph,Haike Reznik‐Wolf,Pnina Langevitz,Avi Livneh,Elon Pras	2010	13
19	A Novel Mutation in theHCN4Gene Causes Symptomatic Sinus Bradycardia in Moroccan Jews Journal of Cardiovascular Electrophysiology ·Avishag Laish‐Farkash,Michael Glikson,Dovrat Brass,Dina Marek‐Yagel,Elon Pras,Nathan Dascal,Charles Antzelevitch,Eyal Nof,HAYA REZNIK,Michael Eldar,David Luria	2010	47
20	Clinical disease among patients heterozygous for familial mediterranean fever Arthritis & Rheumatism ·Dina Marek‐Yagel,Yackov Berkun,Shai Padeh,Almogit Abu,Haike Reznik‐Wolf,Avi Livneh,Mordechai Pras,Elon Pras	2009	152

About Dina Marek‐Yagel

Dina Marek‐Yagel is a scholar working on Clinical Biochemistry, Biochemistry and Gastroenterology, having authored 26 papers that have together received 507 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers), Amino Acid Enzymes and Metabolism (3 papers), Lysosomal Storage Disorders Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), RNA regulation and disease (2 papers), Congenital heart defects research (2 papers) and Helicobacter pylori-related gastroenterology studies (2 papers). The work is most often cited by research in Clinical Biochemistry (63 citations), Biochemistry (50 citations) and Immunology (122 citations). Dina Marek‐Yagel has collaborated with scholars based in Israel, United States and Netherlands. Frequent co-authors include Haike Reznik‐Wolf, Shai Padeh, Avi Livneh, Elon Pras, Yackov Berkun, Mordechai Pras, Yair Anikster, Ortal Barel, Gali Heimer and Eran Eyal. Their work appears in journals such as Digestive Diseases and Sciences, Human Mutation and Human Genetics.

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