HR Waterham

Dikutip oleh

	Semua	Sejak 2020
Kutipan	27495	8856
indeks-h	92	48
indeks-i10	281	194

1900

950

475

1425

199619971998199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242025110 90 134 106 232 255 355 467 541 517 687 782 828 803 948 959 1185 1091 1254 1134 1495 1367 1357 1436 1802 1722 1850 1534 1630 308

Akses publik

Lihat semua

74 artikel

1 artikel

tersedia

tidak tersedia

Berdasarkan pada mandat pendanaan

Pengarang bersama

Sander M. HoutenAssociate Professor, Icahn School of Medicine at Mount SinaiEmail yang diverifikasi di mssm.edu
Ger RijkersUniversity College Roosevelt & Elisabeth Tweesteden Hospital, TilburgEmail yang diverifikasi di ucr.nl
Ron WeversProfessor in Clinical Chemistry in NijmegenEmail yang diverifikasi di radboudumc.nl
Gerbert A. JansenPostdoctoral fellow, Academic Medical Center - University of AmsterdamEmail yang diverifikasi di amc.uva.nl
Stephan KempAmsterdam University Medical Centers, the NetherlandsEmail yang diverifikasi di amsterdamumc.nl
TGJ DerksUniversity of Groningen, University Medical Center GroningenEmail yang diverifikasi di umcg.nl
Prof Tom J de Koning, MD PhD MBAChair department of Pediatrics Lund University Sweden, PI department of Genetics and Neurology, UMCGEmail yang diverifikasi di med.lu.se
Vladimir TitorenkoProfessor of Biology, Concordia UniversityEmail yang diverifikasi di concordia.ca
ke niezen-koninguniversity of groningen, university medical center groningenEmail yang diverifikasi di umcg.nl
Marc EngelenAmsterdam University Medical CentersEmail yang diverifikasi di amc.uva.nl
Riekelt HoutkooperProfessor of Translational Metabolism, Academic Medical Center (AMC), AmsterdamEmail yang diverifikasi di amc.nl
Prof. dr. Jan A.M. SmeitinkProfessor in Mitochondrial MedicineEmail yang diverifikasi di radboudumc.nl
I.J. Klei, van derProfessor Molecular Cell Biology, University of GroningenEmail yang diverifikasi di rug.nl
David R FitzPatrickProfessor & Consultant in Paediatric Genetics, MRC Human Genetics Unit, University of EdinburghEmail yang diverifikasi di nhs.net
Paul CofferUniversity Medical Center UtrechtEmail yang diverifikasi di umcutrecht.nl
Anthony S. WierzbickiConsultant (Honorary Professor) in Metabolic Medicine, Guy's & St Thomas' Hospitals London UKEmail yang diverifikasi di kcl.ac.uk
Frederica TheodoulouScience Director, Plant Sciences for the Bioeconomy, Rothamsted ResearchEmail yang diverifikasi di rothamsted.ac.uk
Aurora PujolProfessor of Genetics and Neuroscience, IDIBELL, ICREA Barcelona SpainEmail yang diverifikasi di idibell.cat
K.J. HellingwerfProfessor emeritus in General microbiology, University of AmsterdamEmail yang diverifikasi di uva.nl
Jorge AzevedoEmail yang diverifikasi di ibmc.up.pt

Ikuti

HR Waterham

Professor Functional Genetics of Metabolic Diseases at University of Amsterdam

Email yang diverifikasi di amc.uva.nl

Metabolism Genetics Translational Research


Judul Urutkan menurut kutipan Urutkan menurut tahun Urutkan menurut judul	Dikutip oleh Dikutip oleh	Tahun
Biochemistry of mammalian peroxisomes revisited RJA Wanders, HR Waterham Annu. Rev. Biochem. 75 (1), 295-332, 2006	1175	2006
A lethal defect of mitochondrial and peroxisomal fission HR Waterham, J Koster, CWT van Roermund, PAW Mooyer, ... New England Journal of Medicine 356 (17), 1736-1741, 2007	876	2007
Isolation of the Pichia pastoris glyceraldehyde-3-phosphate dehydrogenase gene and regulation and use of its promoter HR Waterham, ME Digan, PJ Koutz, SV Lair, JM Cregg Gene 186 (1), 37-44, 1997	687	1997
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome SM Houten, W Kuis, M Duran, TJ De Koning, A van Royen-Kerkhof, ... Nature genetics 22 (2), 175-177, 1999	592	1999
Functions and biosynthesis of plasmalogens in health and disease P Brites, HR Waterham, RJA Wanders Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2004	515	2004
Human disorders of peroxisome metabolism and biogenesis HR Waterham, S Ferdinandusse, RJA Wanders Biochimica Et Biophysica Acta (BBA)-Molecular Cell Research 1863 (5), 922-933, 2016	410	2016
Mutations in the 3β-hydroxysterol Δ24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis HR Waterham, J Koster, GJ Romeijn, RCM Hennekam, P Vreken, ... The American Journal of Human Genetics 69 (4), 685-694, 2001	406	2001
Metabolic interplay between peroxisomes and other subcellular organelles including mitochondria and the endoplasmic reticulum RJA Wanders, HR Waterham, S Ferdinandusse Frontiers in cell and developmental biology 3, 83, 2016	402	2016
Infevers: an evolving mutation database for auto‐inflammatory syndromes I Touitou, S Lesage, M McDermott, L Cuisset, H Hoffman, C Dode, ... Human mutation 24 (3), 194-198, 2004	389	2004
ABCD1 mutations and the X‐linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations S Kemp, A Pujol, HR Waterham, BM Van Geel, CD Boehm, GV Raymond, ... Human mutation 18 (6), 499-515, 2001	378	2001
Peroxisomal fatty acid α- and β-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases RJA Wanders, P Vreken, S Ferdinandusse, GA Jansen, HR Waterham, ... Biochemical Society Transactions 29 (2), 250-267, 2001	365	2001
Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil: frequency of the common IVS14+ 1G> A … ABP van Kuilenburg, EW Muller, J Haasjes, R Meinsma, L Zoetekouw, ... Clinical cancer research 7 (5), 1149-1153, 2001	358	2001
Peroxisomal disorders: the single peroxisomal enzyme deficiencies RJA Wanders, HR Waterham Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1763 (12), 1707-1720, 2006	351	2006
Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy S Ferdinandusse, S Denis, PT Clayton, A Graham, JE Rees, JT Allen, ... Nature genetics 24 (2), 188-191, 2000	335	2000
Genetics and molecular basis of human peroxisome biogenesis disorders HR Waterham, MS Ebberink Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1822 (9 …, 2012	326	2012
The infevers autoinflammatory mutation online registry: update with new genes and functions F Milhavet, L Cuisset, HM Hoffman, R Slim, H El‐Shanti, I Aksentijevich, ... Human mutation 29 (6), 803-808, 2008	326	2008
Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene HR Waterham, FA Wijburg, RCM Hennekam, P Vreken, L Dorland, ... The American Journal of Human Genetics 63 (2), 329-338, 1998	308*	1998
Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact N Shai, E Yifrach, CWT van Roermund, N Cohen, C Bibi, L IJlst, ... Nature communications 9 (1), 1761, 2018	306	2018
Subcellular localization and physiological role of α-methylacyl-CoA racemase S Ferdinandusse, S Denis, L IJlst, G Dacremont, HR Waterham, ... Journal of lipid research 41 (11), 1890-1896, 2000	277	2000
The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters CWT van Roermund, WF Visser, L IJlst, A van Cruchten, M Boek, W Kulik, ... The FASEB Journal 22 (12), 4201-4208, 2008	271	2008

Sistem tidak dapat melakukan operasi ini. Coba lagi nanti.

Artikel 1–20

Kutipan per tahun

Kutipan duplikat

Kutipan yang digabung

Tambahkan pengarang bersamaPengarang bersama

Ikuti

Dikutip oleh

Pengarang bersama