Maian Roifman

1.8k total citations
20 papers, 354 citations indexed

About

Maian Roifman is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Maian Roifman has authored 20 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pediatrics, Perinatology and Child Health, 7 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Maian Roifman's work include Prenatal Screening and Diagnostics (5 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Epigenetics and DNA Methylation (2 papers). Maian Roifman is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Epigenetics and DNA Methylation (2 papers). Maian Roifman collaborates with scholars based in Canada, United States and United Kingdom. Maian Roifman's co-authors include Rosanna Weksberg, Sanaa Choufani, Michal Inbar‐Feigenberg, Darci T. Butcher, David Chitayat, Karen Chong, John‏ Kingdom, Michael Brudno, Andrei L. Turinsky and Sascha Drewlo and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Maian Roifman

18 papers receiving 346 citations

Peers

Maian Roifman

PPCH

GENET

Ana Arpón Spain

Mashael Al‐Shafai Qatar

Bengt Hamark Sweden

Carol Jenkins United Kingdom

Raffael Ott Germany

Ke Hao United States

Shengtian Zhao China

S. Jabara United States

Nicole Y. Souren Netherlands

Amir Hakim United Kingdom

Ana Arpón Spain

Maian Roifman

178 ×0.9

70 ×0.6

PPCH

83 ×1.1

GENET

11 ×0.3

7 ×0.2

Citations per year, relative to Maian Roifman Maian Roifman (= 1×) peers Ana Arpón

Countries citing papers authored by Maian Roifman

Since Specialization

Citations

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

Fields of papers citing papers by Maian Roifman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maian Roifman

This figure shows the co-authorship network connecting the top 25 collaborators of Maian Roifman. A scholar is included among the top collaborators of Maian Roifman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Maian Roifman. Maian Roifman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Yoganathan, Sangeetha, Shaguna Seth, Vivek Pai, et al.. (2025). Cortical Myoclonus in an Adolescent Boy With a De Novo Pathogenic Variant in NUS1 Gene. Neurology. 104(3). e210309–e210309. 2 indexed citations

Ashwal‏, Eran, Susan Blasér, Pradeep Krishnan, et al.. (2023). Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcome. Prenatal Diagnosis. 43(6). 756–762. 1 indexed citations

Roifman, Maian, et al.. (2023). STAT5B germline heterozygous variant presenting with lymphadenopathy, atopy, and short stature. 11(1). 12–18. 1 indexed citations

Merico, Daniele, et al.. (2023). Identification of novel compound heterozygous LRBA mutations associated with recurrent hemophagocytic lymphohistiocytosis and CNS manifestations. 10(1). 20–26.

McCuaig, Jeanna, et al.. (2023). Challenges experienced by genetic counselors while they provided counseling about mosaic embryos. F&S Reports. 4(4). 353–360. 1 indexed citations

Watkins, Nicholas A., Syed Hassan Ejaz Zaidi, Christian R. Marshall, et al.. (2022). Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies. Prenatal Diagnosis. 42(7). 822–830. 14 indexed citations

Roifman, Maian, Brian Hon‐Yin Chung, Diane Reid, et al.. (2021). Heterozygous NOTCH1 deletion associated with variable congenital heart defects. Clinical Genetics. 99(6). 836–841. 8 indexed citations

Li, Dong, Rebecca C. Ahrens‐Nicklas, Janice Baker, et al.. (2020). The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?. American Journal of Medical Genetics Part A. 182(9). 2058–2067. 14 indexed citations

Sinajon, Pierre, David Chitayat, Maian Roifman, et al.. (2019). Microarray and RASopathy‐disorder testing in fetuses with increased nuchal translucency. Ultrasound in Obstetrics and Gynecology. 55(3). 383–390. 35 indexed citations

10.

Chitayat, David, Johannes Keunen, Maian Roifman, et al.. (2019). Impact of introduction of noninvasive prenatal testing on uptake of genetic testing in fetuses with central nervous system anomalies. Prenatal Diagnosis. 39(7). 544–548. 4 indexed citations

11.

Suzuki, Yoshiro, David Chitayat, Hirotake Sawada, et al.. (2018). TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism. The American Journal of Human Genetics. 102(6). 1104–1114. 54 indexed citations

12.

Roifman, Maian, Sanaa Choufani, Andrei L. Turinsky, et al.. (2016). Genome-wide placental DNA methylation analysis of severely growth-discordant monochorionic twins reveals novel epigenetic targets for intrauterine growth restriction. Clinical Epigenetics. 8(1). 70–70. 45 indexed citations

13.

Roifman, Maian, Carlo Marcelis, Tara Paton, et al.. (2014). De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. Clinical Genetics. 87(1). 34–41. 37 indexed citations

14.

Upton, Julia, Bo Ngan, Maian Roifman, et al.. (2014). Hematopoietic stem cell transplantation completely reversed colitis but not arthritis in IL-10Rα deficiency. 1(2). 77–86.

15.

Inbar‐Feigenberg, Michal, Sanaa Choufani, Darci T. Butcher, Maian Roifman, & Rosanna Weksberg. (2013). Basic concepts of epigenetics. Fertility and Sterility. 99(3). 607–615. 117 indexed citations

16.

Ratnapalan, Savithiri, et al.. (2003). Measuring a toddler's mouthful: Toxicologic considerations. The Journal of Pediatrics. 142(6). 729–730. 12 indexed citations

17.

Roifman, Maian, et al.. (2001). Physical Development in Tuvinian Adolescents. International Journal of Circumpolar Health. 60(1). 6–15. 5 indexed citations

18.

Roifman, Maian, et al.. (1989). Elasticity changes in the large arteries of human limbs in response to cycle ergometry performed with upper and lower limbs. European Journal of Applied Physiology. 59(5). 390–397. 1 indexed citations

19.

Roifman, Maian, et al.. (1985). Noninvasive quantitative evaluation of the characteristic impedance modulus of human limb arteries. Bulletin of Experimental Biology and Medicine. 100(4). 1305–1308. 1 indexed citations

20.

Roifman, Maian, et al.. (1983). Effect of posture on elastic properties of the arteries and hemodynamics of human limbs. Bulletin of Experimental Biology and Medicine. 95(1). 5–8. 2 indexed citations

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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