Paldeep S. Atwal

3.1k citations

88 papers · 1.6k indexed · h-index 18

Co-authors: Sarah Macklin Stephanie L. Hines Patrick R. Blackburn Jennifer Gass Fernando Scaglia Eric W. Klee DeLisa Fairweather Jon Sin
Topics: Metabolism and Genetic Disorders (15 papers)Mitochondrial Function and Pathology (10 papers)Connective tissue disorders research (9 papers)
Cited by: Clinical Biochemistry Genetics Molecular Biology
Journals: Proceedings of the National Academy of SciencesSHILAP Revista de lepidopterologíaHepatology
Partner nations: United States United Kingdom Italy

In The Last Decade

Paldeep S. Atwal

85 papers receiving 1.6k citations

Peers

Countries citing papers authored by Paldeep S. Atwal

Since Specialization

Citations

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

Fields of papers citing papers by Paldeep S. Atwal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paldeep S. Atwal. 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 Paldeep S. Atwal. The network helps show where Paldeep S. Atwal may publish in the future.

Co-authorship network of co-authors of Paldeep S. Atwal

This figure shows the co-authorship network connecting the top 25 collaborators of Paldeep S. Atwal. A scholar is included among the top collaborators of Paldeep S. Atwal 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 Paldeep S. Atwal. Paldeep S. Atwal 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

#	Work	Indexed citations
1	Discovery of a MET-driven monogenic cause of steatotic liver disease 2025 ·Hepatology ·Filippo Pinto e Vairo,Michael T. Zimmermann,(unknown),Salomão Dória Jorge,Shulan Tian,Robert A. Vierkant,(unknown),Thiago M. de Assuncao,Angela Mathison,Paldeep S. Atwal,(unknown),Alina M. Allen,Eric W. Klee,Raúl Urrutia,Konstantinos N. Lazaridis	0
2	STRIPE partners in precision medicine series: provider perspective 2024 ·The Pharmacogenomics Journal ·Christine M. Formea,Paldeep S. Atwal,(unknown),Martin Dawes,Gary E. Marchant,(unknown),J. Shawn Jones,(unknown)	1
3	A patient with a novel pathogenic variant in COL5A1 exhibiting prominent vascular and cardiac features 2022 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Houssam Farres,Paldeep S. Atwal	2
4	Importance of Family History in the Era of Exome Analysis: A Report of a Family with Multiple Concurrent Genetic Diseases 2021 ·Human Heredity ·(unknown),(unknown),Jessica K. Abbott,(unknown),Paldeep S. Atwal	1
5	Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling 2020 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),Sarah Macklin,(unknown),(unknown),Daniel F. Broderick,(unknown),Stephanie L. Hines,(unknown),Paldeep S. Atwal,Thomas R. Caulfield	2
6	The infantile neuroaxonal dystrophy rating scale (INAD-RS) 2020 ·Orphanet Journal of Rare Diseases ·Paldeep S. Atwal,Mark Midei,Darius J. Adams,(unknown),(unknown),Peter Milner	8
7	Poirier–Bienvenu neurodevelopmental syndrome: A report of a patient with a pathogenic variant in CSNK2B with abnormal linear growth 2020 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),(unknown),Irman Forghani,Paldeep S. Atwal	11
8	Examination of Molecular Effects ofMYLKDeletion in a Patient with Extensive Aortic, Carotid, and Abdominal Dissections That Underlie the Genetic Dysfunction 2020 ·SHILAP Revista de lepidopterología ·Sarah Macklin,Katelyn A. Bruno,(unknown),(unknown),(unknown),(unknown),Stephanie L. Hines,Paldeep S. Atwal,Thomas R. Caulfield	1
9	Structural Models for the Dynamic Effects of Loss-of-Function Variants in the Human SIM1 Protein Transcriptional Activation Domain 2020 ·Biomolecules ·(unknown),Patrick R. Blackburn,Murray L. Whitelaw,Mieke M. van Haelst,Paldeep S. Atwal,Thomas R. Caulfield	42
10	Protein molecular modeling shows residue T599 is critical to wild-type function of POLG and description of a novel variant associated with the SANDO phenotype 2018 ·Human Genome Variation ·(unknown),(unknown),Elizabeth A. Mauricio,(unknown),Paldeep S. Atwal,Thomas R. Caulfield	6
11	Protein modeling and clinical description of a novel in‐frame GLB1 deletion causing GM1 gangliosidosis type II 2018 ·Molecular Genetics & Genomic Medicine ·(unknown),Michael T. Zimmermann,Patrick R. Blackburn,(unknown),Eric W. Klee,Laura Pollard,Colleen Macmurdo,Paldeep S. Atwal,Thomas R. Caulfield	4
12	Novel variants in COL4A4 and COL4A5 are rare causes of FSGS in two unrelated families 2018 ·Human Genome Variation ·Stephanie L. Hines,(unknown),(unknown),Nabeel Aslam,(unknown),Paldeep S. Atwal	4
13	Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1 2017 ·Hereditary Cancer in Clinical Practice ·Charu Kaiwar,Sarah Macklin,Jennifer Gass,(unknown),Eric W. Klee,Stephanie L. Hines,John Stauffer,Paldeep S. Atwal	1
14	Co‐occurrence of a novel PDGFRB variant and likely pathogenic variant in CASR in an individual with extensive intracranial calcifications and hypocalcaemia 2017 ·Clinical Case Reports ·(unknown),Jeremy D. Burgess,Patrick R. Blackburn,Jennifer Gass,(unknown),(unknown),Jay A. van Gerpen,Paldeep S. Atwal	7
15	BARD1 nonsense variant c.1921C>T in a patient with recurrent breast cancer 2017 ·Clinical Case Reports ·Jennifer Gass,(unknown),Patrick R. Blackburn,Stephanie L. Hines,Paldeep S. Atwal	4
16	Ornithine Transcarbamylase Deficiency: If at First You Do Not Diagnose, Try and Try Again 2017 ·Case Reports in Critical Care ·(unknown),(unknown),(unknown),Paldeep S. Atwal,(unknown)	1
17	Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1 2017 ·Molecular Genetics & Genomic Medicine ·Patrick R. Blackburn,Duygu Selcen,Jennifer Gass,(unknown),Sarah Macklin,Margot A. Cousin,Nicole J. Boczek,Eric W. Klee,Elliot L. Dimberg,Kathleen D. Kennelly,Paldeep S. Atwal	4
18	Expanded phenotype in a patient with spastic paraplegia 7 2017 ·Clinical Case Reports ·Jennifer Gass,Patrick R. Blackburn,(unknown),Sarah Macklin,Jay Van Gerpen,Paldeep S. Atwal	8
19	Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome 2017 ·SHILAP Revista de lepidopterología ·Michael T. Zimmermann,Raúl Urrutia,Patrick R. Blackburn,Margot A. Cousin,Nicole J. Boczek,Eric W. Klee,Colleen Macmurdo,Paldeep S. Atwal	3
20	Mosaic paternal genome‐wide uniparental isodisomy with down syndrome 2015 ·American Journal of Medical Genetics Part A ·(unknown),Paldeep S. Atwal,(unknown),Inder Gadi,Robert Wallerstein	26

About Paldeep S. Atwal

Paldeep S. Atwal is a scholar working on Clinical Biochemistry, Neurology and Genetics, having authored 88 papers that have together received 1.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (10 papers) and Connective tissue disorders research (9 papers). The work is most often cited by research in Clinical Biochemistry (366 citations), Genetics (457 citations) and Molecular Biology (821 citations). Paldeep S. Atwal has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Sarah Macklin, Stephanie L. Hines, Patrick R. Blackburn, Jennifer Gass, Fernando Scaglia, Eric W. Klee, DeLisa Fairweather, Jon Sin, Michael J. Coronado and Damian N. Di Florio. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Hepatology.

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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