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P

Peter Henneman

amsterdam university medical centers
H指数:44
被引数:8,997

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荣誉奖项

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Episignature-based modelled first-tier diagnostic approach in the Dutch Caribbean: advancing equal care through epigenetic classification

基于表观遗传签名的建模一级诊断方法在荷兰加勒比地区的应用：通过表观遗传分类推进平等医疗

Frontiers in Genetics
IF2.8
2026-05-200
OAAI
LV Liselot van der Laan; AL Amanda Luijckx; SL Shirley Lo-A-Njoe; GM Ginette M. Ecury-Goossen; FA Farah A. Falix; SF Sonja Faries; ME Meindert E. Manshande; PA Patricia A. E. A. C. Philippi; EM Evelyn M. van der Plas; HD Hans D. Veenhuis; LR Louise Rafael-Croes; MM Marcel M. A. M. Mannens; BS Bekim Sadikovic; PH Peter Henneman; MA Mariëlle Alders; MM Mieke M. van Haelst
Causal relationship between epigenetic markers and type 2 diabetes in West African populations: a Mendelian randomisation analysis

西非人群中表观遗传标记与2型糖尿病的因果关系：一项孟德尔随机化分析

Diabetologia
IF10.2
2026-04-240
OAAI
Karlijn A. C. Meeks; Eva L. van der Linden; Amy R. Bentley; Ayo P. Doumatey; Peter Henneman; Nora Franceschini; Themistocles L. Assimes; Felix P. Chilunga; Charles F. Hayfron-Benjamin; Ellis Owusu-Dabo; Guanjie Chen; Charles Agyemang; Adebowale A. Adeyemo; Charles N. Rotimi
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects

NOTCH1基因变异的DNA甲基化分析揭示了非综合征性先天性心脏病的第一种表观遗传标志物

Genome Medicine
IF11.2
2026-01-070
OAAI
Gregor Dombrowsky; Liselot van der Laan; Ananília Silva; Jeroen Breckpot; Enrique Audain; Anna Wilsdon; Michael A. Levy; Niels Vos; Marcel Mannens; Jiao Wang; Anjali Jain; Robert Lesurf; David Winlaw; Connie R. Bezzina; Mary Ann Thomas; Almuth Caliebe; Sabine Klaassen; Felix Berger; Sven Dittrich; Brigitte Stiller; Hashim Abdul-Khaliq; Ingo Dähnert; Frances Bu’Lock; Siobhan Loughna; J. David Brook; Seema Mital; Robert B. Russell; Thomas Pickardt; Ulrike Bauer; Hans-Heiner Kramer; Anselm Uebing; Peter Henneman; Bekim Sadikovic; Alex Postma; Marc-Phillip Hitz
Nanopore sequencing enables combined detection of USP7 variants and a known Hao-Fountain syndrome episignature

纳米孔测序技术实现了USP7基因变异与已知的Hao-Fountain综合征表观签名的同时检测。

Frontiers in Genetics
IF2.8
2026-01-050
OAAI
Liselot van der Laan; Martin A. Haagmans; Andrea Venema; Jennifer Kerkhof; Michael A. Levy; Silvana Briuglia; Pilar Caro; Sebastian Sailer; Christian P. Schaaf; Bekim Sadikovic; Mieke M. van Haelst; Mariëlle van Gijn; Mariëlle Alders; Peter Henneman
Exploring the liver kidney axis in the Ghanaian population: the RODAM-Prospective study

探索加纳人群中的肝肾轴：RODAM-前瞻性研究

EUROPEAN JOURNAL OF PUBLIC HEALTH
IF3.9
2025-12-010
OAAI
Mungamba, Muhulo Muhau; Chilunga, Felix. P.; van der Linden, Eva L.; Beune, Erik; Henneman, Peter; Hayfron-Benjamin, Charles F.; Meeks, Karlijn A. C.; Darko, Samuel N.; Twumasi-Ankrah, Sampson; Owusu-Dabo, Ellis; Holleboom, Adriaan G.; Vogt, Liffert; van den Born, Bert-Jan; Chungag, Benedicta N.; Agyemang, Charles
Discovery of a DNA methylation episignature as a molecular biomarker for fetal alcohol syndrome

发现一种DNA甲基化表观签名作为胎儿酒精综合征的分子生物标志物

Genetics in Medicine
IF6.2
2025-09-180
OAAI
Liselot van der Laan; Raissa Relator; Irene Valenzuela; Adri N. Mul; Mariëlle Alders; Michael A. Levy; Jennifer Kerkhof; Jessica Rzasa; Anna M. Cueto-González; Amaia Lasa-Aranzasti; Cristina Cea-Arestin; Marcel M.A.M. Mannens; Mieke M. van Haelst; Eduardo F. Tizzano; Bekim Sadikovic; Peter Henneman
DNA methylation episignature for Smith-Magenis and Potocki-Lupski syndromes: a mirror perspective

DNA甲基化表观签名用于Smith-Magenis和Potocki-Lupski综合征：镜像视角

EUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
2025-09-010
PRE
van der Laan, Liselot; Karimi, Karim; Rooney, Kathleen; Alders, Marielle; Brusco, Alfredo; Lasa-Aranzasti, Amaia; Brunetti-Pierri, Nicola; Cueto-Gonzalez, Anna M.; DuPont, Barbara R.; Cappuccio, Gerarda; Dubourg, Christele; Everman, David; Gatinois, Vincent; Ganne, Benjamin; Genevieve, David; Ferrero, Giovanni Battista; Kempers, Marlies; Levy, Michael A.; Niceta, Marcello; Novelli, Antonio; Orlando, Valeria; Odent, Sylvie; Patterson, Wesley G.; Polstra, Abeltje M.; Roscioli, Tony; Ruiz-Pallares, Nathalie; Sabbagh, Quentin; Trajkova, Slavica; Tartaglia, Marco; Tedder, Matthew A.; Toutain, Annick; Koehler, Udo; Valenzuela, Irena; van Hagen, Johanna M.; van der Kevie-kersemaekers, Anne-Marie; Henneman, Peter; Mannens, Marcel M. A. M.; Sadikovic, Bekim; van Haelst, Mieke M.
An exploratory single-cell analysis of peripheral blood mononuclear cells from vedolizumab-treated Crohn’s disease patients identifies response-associated differences among the plasmacytoid dendritic cells and classical monocytes

一项对vedolizumab治疗的克罗恩病患者外周血单核细胞进行的探索性单细胞分析，识别了浆细胞样树突状细胞和经典单核细胞中与应答相关的差异。

Frontiers in Immunology
IF5.9
2025-08-150
OA
Andrew Yung Fong Li Yim†; Ishtu Hageman†; Vincent W. Joustra†; Ahmed M. I. M. Elfiky; Mohammed Ghiboub; Evgeni Levin; Jan Verhoeff; Caroline Verseijden; Iris Admiraal; Manon de Krijger; Manon E. Wildenberg; Marcel Mannens; Marja E. Jakobs; Susan B. Kenter; Alex T. Adams; Jack Satsangi; Geert R. D’Haens; Wouter J. de Jonge‡; Peter Henneman‡
Development and validation of peripheral blood DNA methylation signatures to predict response to biological therapy in adults with Crohn's disease (EPIC-CD): an epigenome-wide association study

外周血DNA甲基化特征的开发与验证，用于预测成人克罗恩病患者对生物疗法的应答（EPIC-CD）：一项表观基因组-wide关联研究

The Lancet Gastroenterology & Hepatology
IF0
2025-07-010
PRE
Vincent W Joustra; Andrew Y F Li Yim; Peter Henneman; Ishtu Hageman; Tristan de Waard; Evgeni Levin; Alexandra J Noble; Thomas P Chapman; Femke Mol; Sarah van Zon; Donghyeok Lee; Colleen G C McGregor; Melanie S Hulshoff; Jack J Satsangi; Wouter J de Jonge; Geert R D'Haens
CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature
HUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
2025-01-010
OAAI
van der Laan, Liselot; Silva, Ananilia; Kleinendorst, Lotte; Rooney, Kathleen; Haghshenas, Sadegheh; Lauffer, Peter; Alanay, Yasemin; Bhai, Pratibha; Brusco, Alfredo; de Munnik, Sonja; de Vries, Bert B. A.; Vega, Angelica Delgado; Engelen, Marc; Herkert, Johanna C.; Hochstenbach, Ron; Hopman, Saskia; Kant, Sarina G.; Kira, Ryutaro; Kato, Mitsuhiro; Keren, Boris; Kroes, Hester Y.; Levy, Michael A.; Lock-Hock, Ngu; Maas, Saskia M.; Mancini, Grazia M. S.; Marcelis, Carlo; Matsumoto, Naomichi; Mizuguchi, Takeshi; Mussa, Alessandro; Mignot, Cyril; Narhi, Anu; Nordgren, Ann; Pfundt, Rolph; Polstra, Abeltje M.; Trajkova, Slavica; van Bever, Yolande; van den Boogaard, Marie Jose; van der Smagt, Jasper J.; Barakat, Tahsin Stefan; Alders, Marielle; Mannens, Marcel M. A. M.; Sadikovic, Bekim; van Haelst, Mieke M.; Henneman, Peter
DNA methylation episignature and comparative epigenomic profiling for Pitt-Hopkins syndrome caused by TCF4 variants
HUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
2024-07-012
OAAI
van der Laan, Liselot; Lauffer, Peter; Rooney, Kathleen; Silva, Ananilia; Haghshenas, Sadegheh; Relator, Raissa; Levy, Michael A.; Trajkova, Slavica; Huisman, Sylvia A.; Bijlsma, Emilia K.; Kleefstra, Tjitske; van Bon, Bregje W.; Baysal, Ozlem; Zweier, Christiane; Palomares-Bralo, Maria; Fischer, Jan; Szakszon, Katalin; Faivre, Laurence; Piton, Amelie; Mesman, Simone; Hochstenbach, Ron; Elting, Mariet W.; van Hagen, Johanna M.; Plomp, Astrid S.; Mannens, Marcel M. A. M.; Alders, Marielle; van Haelst, Mieke M.; Ferrero, Giovanni B.; Brusco, Alfredo; Henneman, Peter; Sweetser, David A.; Sadikovic, Bekim; Vitobello, Antonio; Menke, Leonie A.
The detection of a strong episignature for Chung-Jansen syndrome, partially overlapping with Börjeson-Forssman-Lehmann and White-Kernohan syndromes
HUMAN GENETICS
IF3.6
2024-05-243
OAAI
Vos, Niels; Haghshenas, Sadegheh; van der Laan, Liselot; Russel, Perle K. M.; Rooney, Kathleen; Levy, Michael A.; Relator, Raissa; Kerkhof, Jennifer; McConkey, Haley; Maas, Saskia M.; Vissers, Lisenka E. L. M.; de Vries, Bert B. A.; Pfundt, Rolph; Elting, Mariet W.; van Hagen, Johanna M.; Verbeek, Nienke E.; Jongmans, Marjolijn C. J.; Lakeman, Phillis; Rumping, Lynne; Bosch, Danielle G. M.; Vitobello, Antonio; Thauvin-Robinet, Christel; Faivre, Laurence; Nambot, Sophie; Garde, Aurore; Willems, Marjolaine; Genevieve, David; Nicolas, Gael; Busa, Tiffany; Toutain, Annick; Gerard, Marion; Bizaoui, Varoona; Isidor, Bertrand; Merla, Giuseppe; Accadia, Maria; Schwartz, Charles E.; Ounap, Katrin; Hoffer, Mariette J. V.; Nezarati, Marjan M.; van den Boogaard, Marie-Jose H.; Tedder, Matthew L.; Rogers, Curtis; Brusco, Alfredo; Ferrero, Giovanni B.; Spodenkiewicz, Marta; Sidlow, Richard; Mussa, Alessandro; Trajkova, Slavica; McCann, Emma; Mroczkowski, Henry J.; Jansen, Sandra; Donker-Kaat, Laura; Duijkers, Floor A. M.; Stuurman, Kyra E.; Mannens, Marcel M. A. M.; Alders, Marielle; Henneman, Peter; White, Susan M.; Sadikovic, Bekim; van Haelst, Mieke M.

研究方向

暂未获取到该数据
M
Marcel M. A. M. Mannens
H 指数:61论文数:228被引数:1.3万
K
Ko Willems van Dijk
H 指数:77论文数:546被引数:2.5万
C
Cornelia M. van Duijn
H 指数:238论文数:1,933被引数:25.2万
A
Andrea Venema
H 指数:19论文数:65被引数:1,358
K
Karlijn Meeks
H 指数:25论文数:129被引数:2,464
M
Mariëlle Alders
H 指数:53论文数:222被引数:1.0万
A
Andrew Y. F. Li Yim
H 指数:14论文数:56被引数:863
B
Bekim Sadiković
H 指数:45论文数:308被引数:6,990
C
Charles Agyemang
H 指数:65论文数:536被引数:1.5万
A
Adebowale Adeyemo
H 指数:77论文数:551被引数:3.2万