Langping He

4.2k total citations
52 papers, 2.0k citations indexed

About

Langping He is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Langping He has authored 52 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 35 papers in Clinical Biochemistry and 6 papers in Genetics. Recurrent topics in Langping He's work include Mitochondrial Function and Pathology (44 papers), Metabolism and Genetic Disorders (35 papers) and ATP Synthase and ATPases Research (22 papers). Langping He is often cited by papers focused on Mitochondrial Function and Pathology (44 papers), Metabolism and Genetic Disorders (35 papers) and ATP Synthase and ATPases Research (22 papers). Langping He collaborates with scholars based in United Kingdom, United States and Germany. Langping He's co-authors include Robert W. Taylor, Robert McFarland, Emma L. Blakely, Douglass M. Turnbull, Patrick F. Chinnery, Andrew M. Schaefer, Roger G. Whittaker, Charlotte L. Alston, Philip G. Griffiths and Gavin Hudson and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Langping He

50 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Langping He United Kingdom	25	1.8k	959	172	152	98	52	2.0k
Emmanuelle Sarzi France	17	1.6k 0.9×	865 0.9×	153 0.9×	109 0.7×	103 1.1×	25	1.7k
Annette Feigenbaum Canada	28	1.7k 0.9×	1.1k 1.2×	160 0.9×	252 1.7×	192 2.0×	61	2.3k
Daria Diodato Italy	18	868 0.5×	535 0.6×	84 0.5×	89 0.6×	88 0.9×	44	1.2k
M. Rimoldi Italy	21	1.2k 0.6×	892 0.9×	183 1.1×	63 0.4×	213 2.2×	58	1.6k
Lynne A. Wolfe United States	15	742 0.4×	297 0.3×	77 0.4×	264 1.7×	120 1.2×	49	1.1k
Alberto Blázquez Spain	18	750 0.4×	323 0.3×	84 0.5×	141 0.9×	129 1.3×	50	1.1k
Alessandra Maresca Italy	18	1.0k 0.6×	264 0.3×	142 0.8×	91 0.6×	132 1.3×	38	1.3k
K Naess Sweden	15	740 0.4×	466 0.5×	76 0.4×	112 0.7×	117 1.2×	41	974
Carla Carducci Italy	17	948 0.5×	818 0.9×	139 0.8×	173 1.1×	216 2.2×	47	1.5k
Saba Tadesse United States	20	1.3k 0.7×	625 0.7×	147 0.9×	116 0.8×	70 0.7×	28	1.5k

Countries citing papers authored by Langping He

Since Specialization

Citations

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

Fields of papers citing papers by Langping He

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Langping He

This figure shows the co-authorship network connecting the top 25 collaborators of Langping He. A scholar is included among the top collaborators of Langping 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 Langping He. Langping He 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

Cabrera‐Orefice, Alfredo, Geoffray Monteuuis, Maria Stensland, et al.. (2025). COA5 has an essential role in the early stage of mitochondrial complex IV assembly. Life Science Alliance. 8(3). e202403013–e202403013.

Edwards, Rachel, Eve Miller‐Hodges, Dawn O’Sullivan, et al.. (2025). Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of Scotland. Neuromuscular Disorders. 49. 105343–105343. 4 indexed citations

Smith, Thomas B., Huw B. Thomas, Kyle Thompson, et al.. (2023). Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54. European Journal of Human Genetics. 31(10). 1190–1194. 3 indexed citations

Steele, Hannah E., Aurora Gómez-Durán, Angela Pyle, et al.. (2020). Metabolic effects of bezafibrate in mitochondrial disease.. Apollo (University of Cambridge).

Steele, Hannah E., Aurora Gómez-Durán, Angela Pyle, et al.. (2020). Metabolic effects of bezafibrate in mitochondrial disease. EMBO Molecular Medicine. 12(3). e11589–e11589. 56 indexed citations

Sommerville, Ewen W., Ilaria Dalla Rosa, Masha M. Rosenberg, et al.. (2019). Identification of a novel heterozygous guanosine monophosphate reductase ( GMPR ) variant in a patient with a late‐onset disorder of mitochondrial DNA maintenance. Clinical Genetics. 97(2). 276–286. 7 indexed citations

Lim, Albert Z., Emma L. Blakely, Langping He, et al.. (2019). A novel pathogenic m.4412G>A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes. Mitochondrion. 47. 18–23. 4 indexed citations

Agnew, Thomas, Michelle Goldsworthy, Carlos Aguilar, et al.. (2018). A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways. Cell Reports. 25(12). 3315–3328.e6. 32 indexed citations

Alston, Charlotte L., Sila Hopton, Langping He, et al.. (2017). Using a quantitative quadruple immunofluorescent assay to diagnose isolated mitochondrial Complex I deficiency. Scientific Reports. 7(1). 15676–15676. 19 indexed citations

10.

Colmenero, Isabel, Nicola Ragge, Emma L. Blakely, et al.. (2016). Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report. BMC Research Notes. 9(1). 325–325. 16 indexed citations

11.

Lax, Nichola Z., Charlotte L. Alston, Katherine Schon, et al.. (2015). Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to NovelRARS2Mutations. Journal of Neuropathology & Experimental Neurology. 74(7). 688–703. 25 indexed citations

12.

Alston, Charlotte L., Emma L. Blakely, Monika Oláhová, et al.. (2015). A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. Human Genetics. 134(8). 869–879. 40 indexed citations

13.

Casey, Jillian P., Ellen Crushell, Kyle Thompson, et al.. (2015). Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1?. JIMD Reports. 26. 13–19. 5 indexed citations

14.

Al‐Hussaini, Abdulrahman, Eissa Faqeih, Ayman W. El‐Hattab, et al.. (2013). Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure. The Journal of Pediatrics. 164(3). 553–559.e2. 36 indexed citations

15.

Lax, Nichola Z., Sharmilee Gnanapavan, Charlotte L. Alston, et al.. (2013). Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA^Glu(MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study. Journal of Neuropathology & Experimental Neurology. 72(2). 164–175. 13 indexed citations

16.

Blakely, Emma L., Robert D. M. Hadden, István Bódi, et al.. (2012). MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle. Neuromuscular Disorders. 22(7). 587–591. 49 indexed citations

17.

Tuppen, Helen, Janev Fehmi, Birgit Czermin, et al.. (2010). Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation. Molecular Genetics and Metabolism. 100(4). 345–348. 24 indexed citations

18.

Swalwell, Helen, Emma L. Blakely, Katarzyna Tońska, et al.. (2008). A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?. European Journal of Human Genetics. 16(10). 1265–1274. 28 indexed citations

19.

Hudson, Gavin, Patrizia Amati‐Bonneau, Emma L. Blakely, et al.. (2007). Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. Brain. 131(2). 329–337. 304 indexed citations

20.

Deschauer, Marcus, Reinhard Kiefer, Emma L. Blakely, et al.. (2003). A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia. Neuromuscular Disorders. 13(7-8). 568–572. 40 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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