Junaid Shabbeer

1.3k total citations
17 papers, 933 citations indexed

About

Junaid Shabbeer is a scholar working on Physiology, Epidemiology and Organic Chemistry. According to data from OpenAlex, Junaid Shabbeer has authored 17 papers receiving a total of 933 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 9 papers in Epidemiology and 5 papers in Organic Chemistry. Recurrent topics in Junaid Shabbeer's work include Lysosomal Storage Disorders Research (11 papers), Trypanosoma species research and implications (9 papers) and Cellular transport and secretion (5 papers). Junaid Shabbeer is often cited by papers focused on Lysosomal Storage Disorders Research (11 papers), Trypanosoma species research and implications (9 papers) and Cellular transport and secretion (5 papers). Junaid Shabbeer collaborates with scholars based in United States, Tunisia and France. Junaid Shabbeer's co-authors include Robert J. Desnick, Makiko Yasuda, Stacy D. Benson, Christine M. Eng, Steve Picton, Wolfgang Schuch, Julie E. Gray, Don Grierson, Kenneth H. Astrin and Grace A. Ashley and has published in prestigious journals such as Nucleic Acids Research, Blood and The American Journal of Human Genetics.

In The Last Decade

Junaid Shabbeer

17 papers receiving 905 citations

Peers

Countries citing papers authored by Junaid Shabbeer

Since Specialization

Citations

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

Fields of papers citing papers by Junaid Shabbeer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Junaid Shabbeer

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Detection of Early Molecular Response (EMR) and Minimal Residual Disease (MRD) in Patients with Diffuse Large B-Cell Lymphoma (DLBCL) Using a Validated Next Generation Sequencing (NGS) Assay for the Detection of Tumor Variants in Circulating Tumor (ct)DNA 2022 ·Blood ·Renee Stokowski, (unknown), Patrick E. Bogard, Coleen R. Hacker, (unknown), Tieming Ji, Teng Li, Vladislava O. Melnikova, Ron McCord, Elizabeth A. Punnoose, Robert D. Loberg, Junaid Shabbeer	4
2	Maternal age trends support uptake of non-invasive prenatal testing (NIPT) in the low-risk population 2018 ·The Journal of Maternal-Fetal & Neonatal Medicine ·(unknown), (unknown), Junaid Shabbeer, (unknown)	20
3	Providing patients with pharmacogenetic test results affects adherence to statin therapy: results of the Additional KIF6 Risk Offers Better Adherence to Statins (AKROBATS) trial 2013 ·The Pharmacogenomics Journal ·(unknown), Barnabie Agatep, (unknown), Bruce J. Schrader, Felix W. Frueh, (unknown), Junaid Shabbeer, James J. Devlin, H. Robert Superko, Eric J. Stanek	35
4	Abstract 290: Statin Adherence in Males and Females, and the Impact of Knowledge of a Genetic Test: Results from the AKROBATS Trial 2012 ·Circulation Cardiovascular Quality and Outcomes ·Scott L. Charland, Barnabie Agatep, Bruce J. Schrader, Felix W. Frueh, Vivian Herrera, (unknown), Junaid Shabbeer, James J. Devlin, (unknown), Eric J. Stanek	2
5	Fabry disease: Identification of 50 novel α-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations 2006 ·Human Genomics ·Junaid Shabbeer, Makiko Yasuda, Stacy D. Benson, Robert J. Desnick	117
6	Detection of ?-galactosidase a mutations causing fabry disease by denaturing high performance liquid chromatography 2005 ·Human Mutation ·Junaid Shabbeer, (unknown), Robert J. Desnick	47
7	Mucopolysaccharidosis type IV: N-Acetylgalactosamine-6-sulfatase mutations in Tunisian patients 2005 ·Molecular Genetics and Metabolism ·Sandrine Laradi, Turgut Tükel, (unknown), Junaid Shabbeer, Mónica Erazo, (unknown), M Chaâbouni, Salima Ferchichi, Abdelhédi Miled, Robert J. Desnick	18
8	Mucopolysaccharidosis I: α‐L‐Iduronidase mutations in three Tunisian families 2005 ·Journal of Inherited Metabolic Disease ·Sandrine Laradi, Turgut Tükel, Mónica Erazo, Junaid Shabbeer, (unknown), (unknown), Salima Ferchichi, M Chaâbouni, Abdelhédi Miled, Robert J. Desnick	22
9	Fabry Disease: Novel α-Galactosidase A 3′-Terminal Mutations Result in Multiple Transcripts Due to Aberrant 3′-End Formation 2003 ·The American Journal of Human Genetics ·Makiko Yasuda, Junaid Shabbeer, Makiko Ōsawa, Robert J. Desnick	35
10	Fabry disease: Characterization of ?-galactosidase A double mutations and the D313Y plasma enzyme pseudodeficiency allele 2003 ·Human Mutation ·Makiko Yasuda, Junaid Shabbeer, Stacy D. Benson, Irène Maire, Roger M. Burnett, Robert J. Desnick	110
11	Fabry disease: 45 novel mutations in the α-galactosidase A gene causing the classical phenotype 2002 ·Molecular Genetics and Metabolism ·Junaid Shabbeer, Makiko Yasuda, Edlira Luca, Robert J. Desnick	78
12	Fabry Disease: Twenty Novel α-Galactosidase A Mutations and Genotype-Phenotype Correlations in Classical and Variant Phenotypes 2002 ·Molecular Medicine ·Dominique P. Germain, Junaid Shabbeer, (unknown), Robert J. Desnick	66
13	Fabry disease: twenty novel α-galactosidase A mutations causing the classical phenotype 2001 ·Journal of Human Genetics ·Grace A. Ashley, Junaid Shabbeer, Makiko Yasuda, Christine M. Eng, Robert J. Desnick	52
14	Fabry disease: twenty-two novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations in severely and mildly affected hemizygotes and heterozygotes. 2000 ·PubMed ·Patrícia Ashton‐Prolla, (unknown), Junaid Shabbeer, Kenneth H. Astrin, Christine M. Eng, Robert J. Desnick	89
15	Twenty Novel Mutations in the α-Galactosidase A Gene Causing Fabry Disease 1999 ·Molecular Medicine ·(unknown), Grace A. Ashley, (unknown), Junaid Shabbeer, Kenneth H. Astrin, Christine M. Eng, Robert J. Desnick	64
16	Analysis of the rabbit cardiac/slow twitch muscle sarcoplasmic reticulum calcium ATPase (SERCA2) gene promoter 1993 ·Nucleic Acids Research ·Drew A. Sukovich, Junaid Shabbeer, Muthu Periasamy	8
17	Molecular biology of fruit ripening and its manipulation with antisense genes 1992 ·Plant Molecular Biology ·Julie E. Gray, Steve Picton, Junaid Shabbeer, Wolfgang Schuch, Don Grierson	166

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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