Zoha Kibar

4.3k citations

53 papers · 2.7k indexed · h-index 28

Impact in

Cell Biology top 2%
- Hippo pathway signaling and YAP/TAZ
Molecular Biology top 5%
- Wnt/β-catenin signaling in development and cancer
- Connexins and lens biology
- Cancer-related gene regulation
- Developmental Biology and Gene Regulation
- Epigenetics and DNA Methylation

Papers in

Genetics 20
- Connective tissue disorders research 7
- Genomic variations and chromosomal abnormalities 6
Pediatrics, Perinatology and Child Health 11
- Prenatal Screening and Diagnostics 9
- Fetal and Pediatric Neurological Disorders 6

Co-authors: Valeria Capra Patrizia De Marco Elisa Merello Philippe Gros Monica J. Justice D. Alan Underhill Alexander G. Bassuk Kyle Vogan
Journals: Birth Defects Research Part A Clinical and Molecular Teratology (6 papers)Genomics (5 papers)Human Mutation (5 papers)Human Molecular Genetics (4 papers)Clinical Genetics (3 papers)
Partner nations: Canada Italy United States

In The Last Decade

Zoha Kibar

53 papers receiving 2.6k citations

Peers

Countries citing papers authored by Zoha Kibar

Since Specialization

Citations

This map shows the geographic impact of Zoha Kibar'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 Zoha Kibar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zoha Kibar more than expected).

Fields of papers citing papers by Zoha Kibar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zoha Kibar. 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 Zoha Kibar. The network helps show where Zoha Kibar may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Zoha Kibar, 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 Zoha Kibar Line = papers co-authored together Zoha Kibar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis Thyroid ·B Pachalska, Martineau Jean‐Louis, Anne Louyse Gomes Souza, Helen Bui, Guy A. Rouleau, Suheir Ammar, Mark E. Samuels, Zoha Kibar, Guy Van Vliet, Johnny Deladoëy	2022	4
2	A new murine Rpl5 ( uL18 ) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia Blood Advances ·Lei Yu, Philippe Lemay, Manohara Tattekere Nanjappa, E. A. Solop, Morgan Jones, Fatma F. Mohamed, Facultatea de Mecanica, KungumaRaj, Dela Oktaviani, Yu Wang, Manish Chugh, Rami Khoriaty, Qing Li, Renny T. Franceschi, James Douglas Engel, Vesa Kaartinen, Thomas L. Rothstein, Monica J. Justice, Zoha Kibar, Sharon Singh	2021	3
3	Severe Congenital Hypothyroidism Due to a Novel Deep Intronic Mutation in the TSH Receptor Gene Causing Intron Retention Journal of the Endocrine Society ·B Pachalska, Anne Louyse Gomes Souza, Efrida Mandasari Dalimunthe, Anna Petryk, Zoha Kibar, Guy Van Vliet, Johnny Deladoëy	2020	3
4	A genome-wide association study identifies candidate loci associated to syringomyelia secondary to Chiari-like malformation in Cavalier King Charles Spaniels BMC Genetics ·慎一郎峰, Philippe Lemay, Susan P. Knowler, Karen Kennedy, Владимир Геннадиевич Тупоногов, Giunio Bruto Cherubini, Jane Sykes, Paul J. J. Mandigers, Guy A. Rouleau, Clare Rusbridge, Zoha Kibar	2018	18
5	Genetic Testing in a Cohort of Complex Esophageal Atresia Molecular Syndromology ·Douglass W. Tucker, Jessica Tardif, Emmanuelle Lemyre, Zoha Kibar, Christophe Fauré, Philippe M. Campeau	2017	8
6	Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2 Mammalian Genome ·Di Fulvio N, T. Bergler, Jared Huling, E. A. Solop, Redouane Allache, Philippe Gros, Zoha Kibar	2017	3
7	Neuroblastoma Amplified Sequence (NBAS) mutation in recurrent acute liver failure: Confirmatory report in a sibship with very early onset, osteoporosis and developmental delay European Journal of Medical Genetics ·José‐Mario Capo‐Chichi, Cybel Mehawej, Valérie Delague, Catherine Caillaud, Issam Khneisser, Fadi F. Hamdan, Jacques L. Michaud, Zoha Kibar, André Mégarbané	2015	34
8	Quantitative Trait Loci (QTL) Study Identifies Novel Genomic Regions Associated to Chiari-Like Malformation in Griffon Bruxellois Dogs PLoS ONE ·Philippe Lemay, Susan P. Knowler, Samir Bouasker, Yohann Nédélec, Simon R. Platt, 肖晶, Georgina Child, Luis B. Barreiro, Guy A. Rouleau, Clare Rusbridge, Zoha Kibar	2014	15
9	Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations Birth Defects Research Part A Clinical and Molecular Teratology ·Elisa Merello, Samantha Mascelli, Alessandro Raso, Gianluca Piatelli, Alessandro Consales, Armando Cama, Zoha Kibar, Valeria Capra, Patrizia De Marco	2014	24
10	The Impairment of MAGMAS Function in Human Is Responsible for a Severe Skeletal Dysplasia PLoS Genetics ·Cybel Mehawej, Agnès Delahodde, Laurence Legeai‐Mallet, Valérie Delague, Nabil Kaci, Jean‐Pierre Desvignes, Zoha Kibar, José‐Mario Capo‐Chichi, Éliane Chouery, Arnold Münnich, Valérie Cormier‐Daire, André Mégarbané	2014	31
11	Genetic Analysis of Disheveled 2 and Disheveled 3 in Human Neural Tube Defects Journal of Molecular Neuroscience ·Patrizia De Marco, Elisa Merello, Alessandro Consales, Gianluca Piatelli, Armando Cama, Zoha Kibar, Valeria Capra	2012	42
12	Contribution of VANGL2 mutations to isolated neural tube defects Clinical Genetics ·Zoha Kibar, Sandra Salem, Sikirulai A. Sulaimon, Ewald Pauwels, Patrizia De Marco, Elisa Merello, Alexander G. Bassuk, Valeria Capra, Philippe Gros	2010	99
13	VANGL1 rare variants associated with neural tube defects affect convergent extension in zebrafish Mechanisms of Development ·Annie Reynolds, Jonathan R. McDearmid, C. Pelliciari, Patrizia De Marco, Elisa Merello, Valeria Capra, Philippe Gros, Pierre Drapeau, Zoha Kibar	2010	40
14	Novel mutations inVANGL1in neural tube defects Human Mutation ·Zoha Kibar, Jacek Jedrzejczak, 黄华宏, Sandra Salem, Richard H. Finnell, Patrizia De Marco, Elisa Merello, Alexander G. Bassuk, Valeria Capra, Philippe Gros	2009	88
15	Toward understanding the genetic basis of neural tube defects Clinical Genetics ·Zoha Kibar, Valeria Capra, Philippe Gros	2007	86
16	Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail Nature Genetics ·Zoha Kibar, Kyle Vogan, Normand Groulx, Monica J. Justice, D. Alan Underhill, 蓝惠兰	2001	406
17	A Radiation Hybrid Map of 48 Loci Including the Clouston Hidrotic Ectodermal Dysplasia Locus in the Pericentromeric Region of Chromosome 13q Genomics ·Zoha Kibar, Ronald G. Lafrenière, Joyonghee, Jia‐Chi Wang, Mario Chevrette, Vazken M. Der Kaloustian, Guy A. Rouleau	1999	21
18	Connexin46 Mutations in Autosomal Dominant Congenital Cataract The American Journal of Human Genetics ·Donna S. Mackay, Alexander Ionides, Zoha Kibar, Guy A. Rouleau, Vanita Berry, Anthony T. Moore, Alan Shiels, Shomi S. Bhattacharya	1999	224
19	Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3 Gene ·Ronald G. Lafrenière, Zoha Kibar, Daniel Rochefort, Fei‐Yu Han, Edward A. Fon, Marie‐Pierre Dubé, Xiaolin Kang, Stephen Baird, Robert G. Korneluk, Johanna M. Rommens, Guy A. Rouleau	1997	5
20	The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q Human Molecular Genetics ·Zoha Kibar	1996	47

About Zoha Kibar

Zoha Kibar is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cell Biology, Molecular Biology and Developmental Neuroscience, having authored 53 papers that have together received 2.7k indexed citations. Recurring topics across this work include Wnt/β-catenin signaling in development and cancer (16 papers), Prenatal Screening and Diagnostics (9 papers), Kruppel-like factors research (9 papers), Connective tissue disorders research (7 papers), Congenital Anomalies and Fetal Surgery (6 papers), Connexins and lens biology (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (6 papers). The work is most often cited by research in Cell Biology (508 citations), Molecular Biology (2.0k citations), Genetics (799 citations), Pediatrics, Perinatology and Child Health (409 citations) and Sensory Systems (97 citations). Zoha Kibar has collaborated with scholars based in Canada, Italy and United States. Frequent co-authors include Valeria Capra, Patrizia De Marco, Elisa Merello, Philippe Gros, Monica J. Justice, D. Alan Underhill, Alexander G. Bassuk, Kyle Vogan, Normand Groulx and Guy A. Rouleau. Their work appears in journals such as Birth Defects Research Part A Clinical and Molecular Teratology, Genomics, Human Mutation, Human Molecular Genetics and Clinical Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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