Harinder Gill

905 total citations
21 papers, 346 citations indexed

About

Harinder Gill is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Harinder Gill has authored 21 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Hematology. Recurrent topics in Harinder Gill's work include Myeloproliferative Neoplasms: Diagnosis and Treatment (7 papers), Chronic Myeloid Leukemia Treatments (4 papers) and Eosinophilic Disorders and Syndromes (3 papers). Harinder Gill is often cited by papers focused on Myeloproliferative Neoplasms: Diagnosis and Treatment (7 papers), Chronic Myeloid Leukemia Treatments (4 papers) and Eosinophilic Disorders and Syndromes (3 papers). Harinder Gill collaborates with scholars based in Canada, Hong Kong and United States. Harinder Gill's co-authors include Miranda Splitt, John Simpson, Gurleen Sharland, Judith Goodship, Michael Wright, Andrew P. Jackson, Gisele E. Ishak, Tracy Dudding, Thomas D. Cushion and Jennifer C. Dempsey and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Journal of the American College of Cardiology.

In The Last Decade

Harinder Gill

16 papers receiving 330 citations

Peers

Countries citing papers authored by Harinder Gill

Since Specialization

Citations

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

Fields of papers citing papers by Harinder Gill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harinder Gill

This figure shows the co-authorship network connecting the top 25 collaborators of Harinder Gill. A scholar is included among the top collaborators of Harinder Gill 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 Harinder Gill. Harinder Gill 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	A clinico-genomic prognostic model for primary myelodysplastic neoplasm in Asia 2025 ·The HKU Scholars Hub (University of Hong Kong) ·Harinder Gill, Rita Yim, Paul Lee, Cheng‐Hong Tsai, (unknown), Garret M. K. Leung, Melissa Ooi, (unknown), Radha Raghupathy, (unknown), (unknown), Qi Zhang, (unknown), Carmen Lee, Wee Joo Chng, Hwei‐Fang Tien, Hsin‐An Hou, Yok‐Lam Kwong	0
2	PARADIGM-PV: a randomized, multicenter phase 4 study to assess the efficacy and safety of ropeginterferon alfa-2b in patients with low- or high-risk polycythemia vera 2025 ·Annals of Hematology ·Abdulraheem Yacoub, Ghaith Abu‐Zeinah, Albert Qin, Tsewang Tashi, (unknown), Weichung Joe Shih, Oleh Zagrijtschuk, (unknown), Robert B. Geller, Norio Komatsu, Ruben A. Mesa, Harinder Gill	0
3	Results from VERIFY, a phase 3, double-blind, placebo (PBO)-controlled study of rusfertide for treatment of polycythemia vera (PV). 2025 ·Journal of Clinical Oncology ·Andrew Kuykendall, Naveen Pemmaraju, Kristen Pettit, Joseph J. Shatzel, Alessandro Lucchesi, Valentín García‐Gutiérrez, Jiří Mayer, Abdulraheem Yacoub, Harinder Gill, (unknown), Daniel Sasca, Joseph M. Scandura, Marina Kremyanskaya, (unknown), Sarita Khanna, Suneel K. Gupta, Arturo Molina, (unknown), (unknown)	0
4	A randomized, double-blind, placebo-controlled phase 3 study to assess efficacy and safety of ropeginterferon alfa-2b in patients with early/lower-risk primary myelofibrosis 2024 ·Annals of Hematology ·Ghaith Abu‐Zeinah, Albert Qin, Harinder Gill, Norio Komatsu, John Mascarenhas, Weichung Joe Shih, Oleh Zagrijtschuk, Toshiaki Sato, Kazuya Shimoda, Richard T. Silver, Ruben A. Mesa	3
5	Bomedemstat (MK3543) in Combination with Ruxolitinib in Patients with Advanced Myelofibrosis 2024 ·Blood ·Harinder Gill, (unknown), (unknown), Rita Yim, Vivian Li, Paul Lee, (unknown), Qi Zhang, (unknown), (unknown), Hugh Young Rienhoff	2
6	Implications of Clonal Hematopoiesis in Hematological and Non-Hematological Disorders 2024 ·Cancers ·Qi Zhang, Rita Yim, Paul Lee, (unknown), (unknown), Harinder Gill	1
7	Somatic mosaicism detected by genome-wide sequencing in 500 parent–child trios with suspected genetic disease: clinical and genetic counseling implications 2021 ·Molecular Case Studies ·(unknown), Linlea Armstrong, Cornelius F. Boerkoel, L. Clarke, Christèle du Souich, Michelle Demos, William T. Gibson, Harinder Gill, Elena Lopez‐Rangel, Millan S. Patel, Kathryn Selby, (unknown), (unknown), Alison M. Elliott, Jan M. Friedman	6
8	Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report 2021 ·BMC Pediatrics ·Géraldine Blanchard‐Rohner, Robert J. Ragotte, Anne Junker, Mehul Sharma, Kate L. Del Bel, Henry Y. Lu, (unknown), (unknown), Harinder Gill, Lori B. Tucker, Richard A. Schreiber, Jacob Rozmus, Catherine M. Biggs, Kyla J. Hildebrand, John K. Wu, Sylvia Stöckler‐Ipsiroglu, Stuart E. Turvey	3
9	The expanding clinical phenotype of germline ABL1 ‐associated congenital heart defects and skeletal malformations syndrome 2020 ·Human Mutation ·Chun‐An Chen, (unknown), Harinder Gill, Tanya N. Nelson, Laurie Robak, Marjolijn C.J. Jongmans, Rolph Pfundt, Chitra Prasad, Roberta Berard, Madeleine Fannemel, Eirik Frengen, Doriana Misceo, Keri Ramsey, Yaping Yang, Christian P. Schaaf, Xia Wang, (unknown)	11
10	Prenatal Autoimmune Disease, Multisystem, Infantile Onset-like Phenotype and Proximal Renal Tubular Dysplasia Associated With STAT3 Mutation 2019 ·Pediatric and Developmental Pathology ·Jefferson Terry, Sylvie Langlois, Rosemarie Rupps, Harinder Gill	3
11	Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder Phenotype 2018 ·Neuroscience ·Gabriella Horváth, Yulin Zhao, Maja Tarailo‐Graovac, Cyrus Boelman, Harinder Gill, Casper Shyr, James Lee, (unknown), Britt I. Drögemöller, (unknown), Colin J.D. Ross, Wyeth W. Wasserman, Andrea Masotti, Paul A. Slesinger, Clara van Karnebeek	20
12	Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes 2015 ·Human Molecular Genetics ·Renske Oegema, Thomas D. Cushion, Ian G. Phelps, Seo‐Kyung Chung, Jennifer C. Dempsey, Sarah Collins, Jonathan G.L. Mullins, Tracy Dudding, Harinder Gill, Andrew Green, William B. Dobyns, Gisele E. Ishak, Mark I. Rees, Dan Doherty	61
13	MG-115 Compound heterozygous SCN4A mutation underlies severe congenital hypotonia and biophysical alteration in the encoded voltage-gated NAV1.4 sodium channel 2015 ·Journal of Medical Genetics ·Clara D.M. van Karnebeek, Xin Ye, Mena Abdelsayed, (unknown), Linhua Zhang, Chieko Chijiwa, Glenda Hendson, Bryan Sayson, Harinder Gill, (unknown), Patrice Eydoux, Colin J.D. Ross, Hilary Vallance, Wyeth W. Wasserman, Peter C. Ruben, M. E. Suzanne Lewis	1
14	Rhabdoid tumor: the Irish experience 1986–2013 2014 ·Cancer Genetics ·(unknown), Harinder Gill, Patrick G. Buckley, (unknown), Michael Capra, (unknown), Michael McDermott, Francesca Brett, Michael Farrell, Jane Pears, Maureen J. O’Sullivan	21
15	Familial distal foregut atresia in a family with likely autosomal dominant inheritance pattern 2012 ·Pediatric Surgery International ·Ian Robinson, Harinder Gill, (unknown), Roisin Hayes	1
16	Delayed diagnosis of 22q11.2 deletion syndrome in an adult Chinese lady. 2012 ·PubMed ·Yat Fung Shea, Chi‐Ho Lee, Harinder Gill, Wing-Sun Chow, Yui‐Ming Lam, Ho‐Ming Luk, (unknown), Leung‐Wing Chu	5
17	Quiz Page October 2010 2010 ·American Journal of Kidney Diseases ·Harinder Gill, (unknown), (unknown), Wai-Kei Lo	2
18	Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart 2009 ·European Journal of Human Genetics ·Harinder Gill, (unknown), C. Mirella Spalluto, Angela Davies, (unknown), (unknown), Bee Ling Ng, Nigel P. Carter, Caroline Mackie Ogilvie, David I. Wilson, Roland G. Roberts	9
19	Patterns of recurrence of congenital heart disease 2003 ·Journal of the American College of Cardiology ·Harinder Gill, Miranda Splitt, Gurleen Sharland, John Simpson	121
20	Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24 2000 ·The American Journal of Human Genetics ·Judith Goodship, Harinder Gill, (unknown), Andrew P. Jackson, Miranda Splitt, Michael Wright	76

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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