Langping He

4.3k citations

52 papers · 2.1k · h-index 25

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Molecular Biology top 5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA Research and Splicing

Papers in

Molecular Biology 49
- Mitochondrial Function and Pathology 43
- ATP Synthase and ATPases Research 15
- RNA modifications and cancer 11
- RNA and protein synthesis mechanisms 4
- RNA Research and Splicing 3
Clinical Biochemistry 26
- Metabolism and Genetic Disorders 26

Co-authors: Robert W. Taylor (52 shared papers)Robert McFarland (24 shared papers)Emma L. Blakely (20 shared papers)Douglass M. Turnbull (16 shared papers)Patrick F. Chinnery (10 shared papers)Andrew M. Schaefer (6 shared papers)Roger G. Whittaker (1 shared paper)Charlotte L. Alston (18 shared papers)
Journals: Neuromuscular Disorders (5 papers)European Journal of Human Genetics (4 papers)Neurology Genetics (3 papers)Journal of Neuropathology & Experimental Neurology (2 papers)Annals of Neurology (2 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Langping He

51 papers receiving 2.1k citations

Peers

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-authors

The 25 scholars most cited alongside Langping He, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Langping He Line = papers co-authored together Langping He links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 52 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Prevalence of mitochondrial DNA disease in adults Annals of Neurology ·Andrew M. Schaefer, Robert McFarland, Emma L. Blakely, Langping He, Roger G. Whittaker, Robert W. Taylor, Patrick F. Chinnery, Douglass M. Turnbull	2007	459
2	Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance Brain ·Gavin Hudson, Patrizia Amati‐Bonneau, Emma L. Blakely, Joanna D. Stewart, Langping He, Andrew M. Schaefer, Philip G. Griffiths, Kati J. Ahlqvist, Anu Suomalainen, Pascal Reynier, Robert McFarland, Douglass M. Turnbull, Patrick F. Chinnery, Robert W. Taylor	2007	327
3	Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA PLoS Genetics ·John W. Yarham, Tek N. Lamichhane, Angela Pyle, Sandy Mattijssen, Enrico Baruffini, Francesco Bruni, Claudia Donnini, Alex Vassilev, Langping He, Emma L. Blakely, Helen Griffin, Mauro Santibanez‐Koref, Laurence A. Bindoff, Ileana Ferrero, Patrick F. Chinnery, Robert McFarland, Richard J Maraia, Robert W. Taylor	2014	105
4	Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure Cardiovascular Pathology ·Annalinda Pisano, Bruna Cerbelli, Elena Perli, Maria Pelullo, Valentina Bargelli, Carmela Preziuso, Massimiliano Mancini, Langping He, Matthew Bates, J. Lucena, Paola Lilla Della Monica, Giuseppe Familiari, Vincenzo Petrozza, Chiara Nediani, Robert W. Taylor, Giulia d’Amati, Carla Giordano	2015	75
5	The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families Brain ·Helen Tuppen, Vanessa Hogan, Langping He, Emma L. Blakely, Lisa Worgan, Mazhor Aldosary, Gabriele Saretzki, Charlotte L. Alston, Andrew A. M. Morris, Michael A. Clarke, Simon Jones, Anita Devlin, Sahar Mansour, Zofia M. Chrzanowska‐Lightowlers, David R. Thorburn, Robert McFarland, Robert W. Taylor	2010	71
6	Metabolic effects of bezafibrate in mitochondrial disease EMBO Molecular Medicine ·Hannah E. Steele, Aurora Gómez-Durán, Angela Pyle, Sila Hopton, Jane Newman, Renae J. Stefanetti, Sarah J. Charman, Jehill Parikh, Langping He, Carlo Viscomi, Djordje G. Jakovljević, Kieren G. Hollingsworth, Alan J. Robinson, Robert W. Taylor, Leonardo Bottolo, Rita Horváth, Patrick F. Chinnery	2020	60
7	Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Abdulraheem Ali Almalki, Charlotte L. Alston, Alasdair Parker, Ingrid Simonic, Sarju Mehta, Langping He, Mojgan Reza, Jorge M.A. Oliveira, Robert N. Lightowlers, Robert McFarland, Robert W. Taylor, Zofia M. Chrzanowska‐Lightowlers	2013	56
8	MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle Neuromuscular Disorders ·Emma L. Blakely, Anna Butterworth, Robert D. M. Hadden, István Bódi, Langping He, Robert McFarland, Robert W. Taylor	2012	54
9	Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure The Journal of Pediatrics ·Abdulrahman Al‐Hussaini, Eissa Faqeih, Ayman W. El‐Hattab, Majid Alfadhel, Ali Asery, Badr Alsaleem, Eman Bakhsh, Ashraf Ali, Ali Alasmari, Khurram Lone, Ahmed Nahari, Wafaa Eyaid, Mohammed Al Balwi, Kate Craig, Anna Butterworth, Langping He, Robert W. Taylor	2013	45
10	A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency Human Genetics ·Charlotte L. Alston, Camilla Ceccatelli Berti, Emma L. Blakely, Monika Oláhová, Langping He, Colin J. McMahon, S. E. Olpin, Iain P. Hargreaves, Cecilia Nolli, Robert McFarland, P Goffrini, Maureen J. O’Sullivan, Robert W. Taylor	2015	44
11	A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia Neuromuscular Disorders ·Marcus Deschauer, Reinhard Kiefer, Emma L. Blakely, Langping He, Stephan Zierz, Douglass M. Turnbull, Robert W. Taylor	2003	43
12	Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency The American Journal of Human Genetics ·Charlotte L. Alston, Mike T. Veling, Juliana Heidler, Lucie S Taylor, Joseph T. Alaimo, Andrew Y. Sung, Langping He, Sila Hopton, Alexander Broomfield, Julija Pavaine, Jullianne Diaz, Eyby Leon, Philipp Wolf, Robert McFarland, Holger Prokisch, Saskia B. Wortmann, Penelope E. Bonnen, Ilka Wittig, David J. Pagliarini, Robert W. Taylor	2019	42
13	A New Mitochondrial Transfer RNAPro Gene Mutation Associated With Myoclonic Epilepsy With Ragged-Red Fibers and Other Neurological Features Archives of Neurology ·Emma L. Blakely, S. Anand Trip, Helen Swalwell, Langping He, Damian Wren, Philip Rich, Douglass M. Turnbull, Salah Omer, Robert W. Taylor	2009	40
14	Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathy Neuromuscular Disorders ·Emma L. Blakely, Langping He, Julie L. Gardner, Gavin Hudson, John H. Walter, Imelda Hughes, Douglass M. Turnbull, Robert W. Taylor	2008	37
15	Somatic Mitochondrial DNA Deletions Accumulate to High Levels in Aging Human Extraocular Muscles Investigative Ophthalmology & Visual Science ·Patrick Yu‐Wai‐Man, Joey E. Lai‐Cheong, Gillian M. Borthwick, Langping He, Geoffrey A. Taylor, Laura C. Greaves, Robert W. Taylor, Philip G. Griffiths, Douglass M. Turnbull	2010	36
16	The m.5650G > A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy Neuromuscular Disorders ·Robert McFarland, Helen Swalwell, Emma L. Blakely, Langping He, Emma J. Groen, Douglass M. Turnbull, Kate Bushby, Robert W. Taylor	2007	35
17	Pathological mechanisms underlying single large‐scale mitochondrial DNA deletions Annals of Neurology ·Mariana C. Rocha, Hannah S. Rosa, John P. Grady, Emma L. Blakely, Langping He, Nadine Romain, Ronald G. Haller, Jane Newman, Robert McFarland, Yi Shiau Ng, Gráinne S. Gorman, Andrew M. Schaefer, Helen Tuppen, Robert W. Taylor, Douglass M. Turnbull	2017	34
18	The clinical spectrum of the m.10191T>C mutation in complex I‐deficient Leigh syndrome Developmental Medicine & Child Neurology ·Victoria Nesbitt, Patrick J. Morrison, Ellen Crushell, Deirdre E. Donnelly, Charlotte L. Alston, Langping He, Robert McFarland, Robert W. Taylor	2012	32
19	A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways Cell Reports ·Thomas Agnew, Michelle Goldsworthy, Carlos Aguilar, Anna Morgan, Michelle Simon, Helen Hilton, Chris Esapa, Yixing Wu, Heather Cater, Liz Bentley, Cheryl L. Scudamore, Joanna Poulton, Karl Morten, Kyle Thompson, Langping He, Steve D. M. Brown, Robert W. Taylor, Michael R. Bowl, Roger Cox	2018	32
20	Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Petter Schandl Sanaker, Marina Toompuu, Vanessa Hogan, Langping He, Charalampos Tzoulis, Zofia M. Chrzanowska‐Lightowlers, Robert W. Taylor, Laurence A. Bindoff	2010	30

About Langping He

Langping He is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine, having authored 52 papers that have together received 2.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (43 papers), Metabolism and Genetic Disorders (26 papers), ATP Synthase and ATPases Research (15 papers), RNA modifications and cancer (11 papers), RNA and protein synthesis mechanisms (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic Neurodegenerative Diseases (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Clinical Biochemistry (922 citations), Molecular Biology (1.9k citations), Aging (17 citations), Cellular and Molecular Neuroscience (172 citations) and Neurology (60 citations). Langping He has collaborated with scholars based in United Kingdom, United States and Germany. Frequent 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, Gavin Hudson and Philip G. Griffiths. Their work appears in journals such as Neuromuscular Disorders, European Journal of Human Genetics, Neurology Genetics, Journal of Neuropathology & Experimental Neurology and Annals of Neurology.

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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