Ning He

1.0k total citations
16 papers, 610 citations indexed

About

Ning He is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ning He has authored 16 papers receiving a total of 610 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Surgery. Recurrent topics in Ning He's work include Genetic and Kidney Cyst Diseases (8 papers), Renal and related cancers (8 papers) and Genetic Syndromes and Imprinting (5 papers). Ning He is often cited by papers focused on Genetic and Kidney Cyst Diseases (8 papers), Renal and related cancers (8 papers) and Genetic Syndromes and Imprinting (5 papers). Ning He collaborates with scholars based in Canada, United States and China. Ning He's co-authors include York Pei, Patrick S. Parfrey, Peter St George‐Hyslop, Gregory G. Germino, Terry Watnick, Kairong Wang, Andrew D. Paterson, Yan Liang, Stefan Somlo and Donna Hefferton and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and Kidney International.

In The Last Decade

Ning He

15 papers receiving 598 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ning He Canada	11	443	441	106	86	66	16	610
Anne Grall-Jézéquel France	3	257 0.6×	348 0.8×	71 0.7×	74 0.9×	32 0.5×	3	424
Loes van Keimpema Netherlands	10	250 0.6×	610 1.4×	29 0.3×	126 1.5×	285 4.3×	12	643
Xiangyi Jing China	13	197 0.4×	171 0.4×	14 0.1×	20 0.2×	68 1.0×	52	410
Magdalena Żołędziewska Italy	12	135 0.3×	176 0.4×	16 0.2×	27 0.3×	33 0.5×	30	382
Christian Vasseur France	4	459 1.0×	65 0.1×	84 0.8×	7 0.1×	54 0.8×	6	553
Lauren Weintraub United States	11	118 0.3×	52 0.1×	40 0.4×	20 0.2×	66 1.0×	28	408
Jalel Chemli Tunisia	11	73 0.2×	75 0.2×	19 0.2×	40 0.5×	21 0.3×	44	359
V. Steinbicker Germany	7	196 0.4×	183 0.4×	13 0.1×	26 0.3×	39 0.6×	16	301
Sophie Gié France	6	87 0.2×	77 0.2×	247 2.3×	16 0.2×	16 0.2×	7	447
Anna Materna‐Kiryluk Poland	13	153 0.3×	170 0.4×	4 0.0×	33 0.4×	100 1.5×	37	403

Countries citing papers authored by Ning He

Since Specialization

Citations

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

Fields of papers citing papers by Ning He

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ning He

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

He, Yuanfang, Xiaoliang He, Ning He, et al.. (2025). Epidemiological trends and pathogen analysis of pediatric acute respiratory infections in Hanzhong Hospital, China: insights from 2023 to 2024. Frontiers in Public Health. 13. 1557076–1557076.

Huang, Feng, et al.. (2023). Identification and fine mapping of a new bacterial blight resistance gene, Xa43(t), in Zhangpu wild rice (Oryza rufipogon). Plant Biology. 25(3). 433–439. 7 indexed citations

Iliuta, Ioan-Andrei, Matthew B. Lanktree, Marina Pourafkari, et al.. (2023). Atypical Polycystic Kidney Disease as defined by Imaging. Scientific Reports. 13(1). 2952–2952. 11 indexed citations

Lanktree, Matthew B., Elsa Guiard, Marina Pourafkari, et al.. (2021). Patients with Protein-Truncating PKD1 Mutations and Mild ADPKD. Clinical Journal of the American Society of Nephrology. 16(3). 374–383. 19 indexed citations

Hayes, Kaleen N., Ning He, Kevin A. Brown, et al.. (2021). Over half of seniors who start oral bisphosphonate therapy are exposed for 3 or more years: novel rolling window approach and patterns of use. Osteoporosis International. 32(7). 1413–1420. 10 indexed citations

Hussain, Hamidah, et al.. (2019). Tuberculosis in Canada: 2017. Canada Communicable Disease Report. 45(2/3). 68–74. 44 indexed citations

Lanktree, Matthew B., Elsa Guiard, Weili Li, et al.. (2019). Intrafamilial Variability of ADPKD. Kidney International Reports. 4(7). 995–1003. 39 indexed citations

Hussain, Hamidah, et al.. (2019). La tuberculose au Canada : 2017. Relevé des maladies transmissibles au Canada. 45(2/3). 73–80. 1 indexed citations

Robitaille, Pierre, Aïcha Mérouani, Ning He, & York Pei. (2011). Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness. European Journal of Pediatrics. 170(9). 1209–1211. 10 indexed citations

10.

Pei, York, Lan Zheng, Kairong Wang, et al.. (2011). A missense mutation in PKD1 attenuates the severity of renal disease. Kidney International. 81(4). 412–417. 46 indexed citations

11.

Çil, Onur, et al.. (2009). Evidence for Pathogenicity of Atypical Splice Mutations in Autosomal Dominant Polycystic Kidney Disease. Clinical Journal of the American Society of Nephrology. 4(2). 442–449. 12 indexed citations

12.

He, Ning, Alireza Zahirieh, Brian Lee, et al.. (2006). Recessive NPHS2 (Podocin) Mutations Are Rare in Adult-Onset Idiopathic Focal Segmental Glomerulosclerosis. Clinical Journal of the American Society of Nephrology. 2(1). 31–37. 44 indexed citations

13.

Paterson, Andrew D., Riccardo Magistroni, Ning He, et al.. (2005). Progressive Loss of Renal Function Is an Age-Dependent Heritable Trait in Type 1 Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology. 16(3). 755–762. 63 indexed citations

14.

Zahirieh, Alireza, M. Andrew Nesbit, Asif Ali, et al.. (2005). Functional Analysis of a Novel GATA3 Mutation in a Family with the Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome. The Journal of Clinical Endocrinology & Metabolism. 90(4). 2445–2450. 42 indexed citations

15.

Pei, York, Andrew D. Paterson, Ning He, et al.. (2001). Bilineal Disease and Trans-Heterozygotes in Autosomal Dominant Polycystic Kidney Disease. The American Journal of Human Genetics. 68(2). 355–363. 117 indexed citations

16.

Pei, York, Terry Watnick, Ning He, et al.. (1999). Somatic PKD2 Mutations in Individual Kidney and Liver Cysts Support a “Two-Hit” Model of Cystogenesis in Type 2 Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology. 10(7). 1524–1529. 145 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.

Explore authors with similar magnitude of impact