M. Tuchman

491 total citations
8 papers, 238 citations indexed

About

M. Tuchman is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, M. Tuchman has authored 8 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Genetics. Recurrent topics in M. Tuchman's work include Genetic and Kidney Cyst Diseases (3 papers), Metabolism and Genetic Disorders (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). M. Tuchman is often cited by papers focused on Genetic and Kidney Cyst Diseases (3 papers), Metabolism and Genetic Disorders (3 papers) and Amino Acid Enzymes and Metabolism (2 papers). M. Tuchman collaborates with scholars based in United States, United Kingdom and Denmark. M. Tuchman's co-authors include William A. Gahl, Meral Gunay‐Aygun, Joy Bryant, Esperanza Font–Montgomery, Theo Heller, Barış Türkbey, Peter L. Choyke, Kailash Daryanani, Marjan Huizing and Orit Reish and has published in prestigious journals such as The Journal of Pediatrics, Molecular Genetics and Metabolism and Cytogenetic and Genome Research.

In The Last Decade

M. Tuchman

8 papers receiving 234 citations

Peers

M. Tuchman

GENET

MB

SURGE

CB

PPCH

Matanel Yheskel United States

Fernanda Caroline Soardi Brazil

C. R. Greenberg Canada

Masaki Wake Japan

Nithiwat Vatanavicharn Thailand

Philip L. Beales United Kingdom

Sherly Pardo Puerto Rico

Aristeidis Giannakopoulos Greece

Yael Wilnai United States

Shun‐Ping Chang Taiwan

Matanel Yheskel United States

M. Tuchman

191 ×1.3

GENET

260 ×1.8

MB

26 ×0.5

SURGE

13 ×0.3

CB

17 ×0.5

PPCH

Citations per year, relative to M. Tuchman M. Tuchman (= 1×) peers Matanel Yheskel

Countries citing papers authored by M. Tuchman

Since Specialization

Citations

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

Fields of papers citing papers by M. Tuchman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Tuchman

This figure shows the co-authorship network connecting the top 25 collaborators of M. Tuchman. A scholar is included among the top collaborators of M. Tuchman 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 M. Tuchman. M. Tuchman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Gunay‐Aygun, Meral, M. Tuchman, Esperanza Font–Montgomery, et al.. (2009). PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis. Molecular Genetics and Metabolism. 99(2). 160–173. 66 indexed citations

2.

Gunay‐Aygun, Meral, Melissa A. Parisi, Dan Doherty, et al.. (2009). MKS3-Related Ciliopathy with Features of Autosomal Recessive Polycystic Kidney Disease, Nephronophthisis, and Joubert Syndrome. The Journal of Pediatrics. 155(3). 386–392.e1. 20 indexed citations

3.

Westbroek, Wendy, M. Tuchman, Olivier De Wever, et al.. (2008). A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome. Molecular Genetics and Metabolism. 94(2). 248–254. 23 indexed citations

4.

Türkbey, Barış, İclal Ocak, Kailash Daryanani, et al.. (2008). Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF). Pediatric Radiology. 39(2). 100–111. 69 indexed citations

5.

Tuchman, M., et al.. (1998). Polymorphisms in the human ornithine transcarbamylase gene useful for allele tracking. Mutations in brief no. 193. Online.. PubMed. 12(4). 289–90. 6 indexed citations

6.

Summar, Marshall, et al.. (1995). Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35. Cytogenetic and Genome Research. 71(3). 266–267. 29 indexed citations

7.

Reish, Orit, Robert Plante, & M. Tuchman. (1993). Four New Mutations in the Ornithine Transcarbamylase Gene. Biochemical Medicine and Metabolic Biology. 50(2). 169–175. 18 indexed citations

8.

Sofer, Cyril & M. Tuchman. (1970). Appraisal Interviews and the Structure of Colleague Relations. The Sociological Review. 18(3). 365–391. 7 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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