Langping He

4.3k citations

71 papers · 3.6k · h-index 33

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Molecular Biology top 2%
- Mitochondrial Function and Pathology
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- Muscle Physiology and Disorders

Papers in

Molecular Biology 70
- Mitochondrial Function and Pathology 66
- Muscle Physiology and Disorders 3
- RNA and protein synthesis mechanisms 1
- RNA Research and Splicing 1
Clinical Biochemistry 14
- Metabolism and Genetic Disorders 14

Co-authors: Robert William Taylor (54 shared papers)Robert McFarland (26 shared papers)Emma L. Blakely (22 shared papers)Douglass M. Turnbull (16 shared papers)Patrick Francis Chinnery (10 shared papers)Andrew M. Schaefer (6 shared papers)Roger G. Whittaker (1 shared paper)Charlotte L. Alston (20 shared papers)
Journals: The American Journal of Human Genetics (8 papers)Neuromuscular Disorders (5 papers)European Journal of Human Genetics (4 papers)Brain (4 papers)Neurology Genetics (3 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Langping He

71 papers receiving 3.5k 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 71 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 William Taylor, Patrick Francis Chinnery, Douglass M. Turnbull	2007	472
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	2007	352
3	Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies JAMA ·Robert William Taylor, Angela Pyle, Helen R Griffin, Emma L. Blakely, Jennifer Duff, Langping He, Tania Smertenko, Charlotte L. Alston	2014	316
4	Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance The American Journal of Human Genetics ·Penelope E. Bonnen, John W. Yarham, Arnaud Besse, Ping Chun Wu, Eissa Faqeih, Ali Alasmari, Mohammad A. M. Saleh, Wafaa Eyaid	2013	147
5	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 P. Vassilev	2014	118
6	Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number The American Journal of Human Genetics ·Kyle Thompson, Homa Majd, Cristina Dallabona, Karit Reinson, Martin S. King, Charlotte L. Alston, Langping He, Tiziana Lodi	2016	111
7	Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies The American Journal of Human Genetics ·Metodi Dimitrov Metodiev, Kyle Thompson, Charlotte L. Alston, A. A. M. Morris, Langping He, Zarah Assouline, Marlène Rio, Nadia Bahi‐Buisson	2016	104
8	LRPPRCmutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population Brain ·Monika Oláhová, Steven A. Hardy, Julie Hall, John W. Yarham, Tobias B. Haack, William C. Wilson, Charlotte L. Alston, Langping He	2015	87
9	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	2015	79
10	The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families Brain ·Helen A. L. Tuppen, Vanessa E. Hogan, Langping He, Emma L. Blakely, Lisa C. Worgan, Mazhor S. Aldosary, Gabriele Christine Saretzki, Charlotte L. Alston	2010	73
11	Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics Brain ·Robert D. S. Pitceathly, Conrad Smith, Carl Fratter, Charlotte L. Alston, Langping He, Kate Craig, Emma L. Blakely, Julie Evans	2012	69
12	Metabolic effects of bezafibrate in mitochondrial disease EMBO Molecular Medicine ·Hannah E. Steele, Aurora Gómez-Durán, Angela Pyle, Sila Hopton, Jane H. Newman, Renae J. Stefanetti, Sarah J. Charman, Jehill D. Parikh	2020	68
13	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 G. Mehta, Langping He, Mojgan Reza, Jorge M. A. Oliveira	2013	66
14	OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect EMBO Molecular Medicine ·Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialò, Luke E. Formosa, David A. Stroud, Madeleine Garrett, Nichola Zoe Lax	2018	66
15	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 William Taylor	2012	58
16	Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype The American Journal of Human Genetics ·Charlotte L. Alston, Alison G. Compton, Luke E. Formosa, Valentina Strecker, Monika Oláhová, Tobias B. Haack, Joél Smet, Katrien Stouffs	2016	55
17	Clinical and Molecular Characteristics of Mitochondrial DNA Depletion Syndrome Associated with Neonatal Cholestasis and Liver Failure The Journal of Pediatrics ·Abdulrahman A. Al‐Hussaini, Eissa Faqeih, Ayman W. El‐Hattab, Majid Alfadhel, Ali Asery, Badr Alsaleem, Eman Bakhsh, Ashraf Ali	2013	53
18	Clinical Features, Molecular Heterogeneity, and Prognostic Implications in YARS2-Related Mitochondrial Myopathy JAMA Neurology ·Ewen W. Sommerville, Yi Shiau Ng, Charlotte L. Alston, Cristina Dallabona, Micol Gilberti, Langping He, Charlotte V. Y. Knowles, Sophie L. Chin	2017	53
19	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 Joseph McMahon, Simon Edward Olpin, Iain Parry Hargreaves	2015	47
20	A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C‐methyltransferase deficiency Human Mutation ·May Christine V. Malicdan, Thierry Vilboux, Bruria Ben Zeev, Jennifer Guo, Aviva Eliyahu, Ben Pode‐Shakked, Amir Dori, Sravan Kakani	2017	46

About Langping He

Langping He is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 71 papers that have together received 3.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (66 papers), Metabolism and Genetic Disorders (14 papers), Genomics and Rare Diseases (5 papers), Muscle Physiology and Disorders (3 papers), Genetic Neurodegenerative Diseases (1 paper), RNA and protein synthesis mechanisms (1 paper), RNA Research and Splicing (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Clinical Biochemistry (518 citations), Molecular Biology (2.9k citations), Genetics (351 citations), Cellular and Molecular Neuroscience (151 citations) and Aging (12 citations). Langping He has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Robert William Taylor, Robert McFarland, Emma L. Blakely, Douglass M. Turnbull, Patrick Francis Chinnery, Andrew M. Schaefer, Roger G. Whittaker, Charlotte L. Alston, Gavin Hudson and Philip G. Griffiths. Their work appears in journals such as The American Journal of Human Genetics, Neuromuscular Disorders, European Journal of Human Genetics, Brain and Neurology Genetics.

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