Martina Wilke

3.0k citations

52 papers · 1.6k indexed · h-index 22

Hematology top 5%
- Hematopoietic Stem Cell Transplantation 5
Pulmonary and Respiratory Medicine top 5%
- Cystic Fibrosis Research Advances 17
- Neonatal Respiratory Health Research 7
Immunology top 10%
- Immunotherapy and Immune Responses 8
- T-cell and B-cell Immunology 8
- Immune Cell Function and Interaction 6
Genetics top 10%
- Genomics and Rare Diseases 5
Molecular Biology
- Congenital heart defects research 4

Co-authors: Bob J. Scholte Hugo R. de Jonge Huub Jorna Els Goulmy Alice G.M. Bot Elisabetta Fortunati Frédéric Becq Sabrina Noël
Cited by: Hematology Pulmonary and Respiratory Medicine Immunology
Journals: Journal of Cystic Fibrosis (4 papers)European Journal of Medical Genetics (2 papers)American Journal of Physiology-Lung Cellular and Molecular Physiology (2 papers)
Partner nations: Netherlands Germany United States

In The Last Decade

Martina Wilke

52 papers receiving 1.5k citations

Peers

Countries citing papers authored by Martina Wilke

Since Specialization

Citations

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

Fields of papers citing papers by Martina Wilke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Martina Wilke, 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 Martina Wilke Line = papers co-authored together Martina Wilke links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Two novel variants in GRN: the relevance of CNV analysis and genetic screening in FTLD patients with a negative family history Journal of Neurology ·С И Данилин,Elise G.P. Dopper,P. Marcus,Norman Butler,Marina Arcaro,Daniela Galimberti,Guido J. Breedveld,Martina Wilke,Rick van Minkelen,Lize C. Jiskoot,John C. van Swieten,Laura Donker Kaat,Harro Seelaar	2024	1
2	5,10‐methenyltetrahydrofolate synthetase deficiency: An extreme rare defect of folate metabolism in two Dutch siblings JIMD Reports ·Nowakowska,Desirée E.C. Smith,Hidde H. Huidekoper,Shih-Ping Kao,Mirjam M. C. Wamelink,Marie‐Claire Y. de Wit,Martina Wilke,George J. G. Ruijter,Jörgen Bierau,Henk J. Blom	2024	1
3	The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis European Journal of Medical Genetics ·Karin E. M. Diderich,Garima Gupta,Vyne van der Schoot,Myrthe van den Born,Martina Wilke,Marieke Joosten,Kyra E. Stuurman,Lies H. Hoefsloot,Diane Van Opstal,Hennie T. Brüggenwirth,Malgorzata I. Srebniak	2023	6
4	EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: State of the art 2023 Andrology ·Csilla Krausz,Paulo Navarro‐Costa,Martina Wilke,Frank Tüttelmann	2023	23
5	Integration of metabolomics with genomics: Metabolic gene prioritization using metabolomics data and genomic variant (CADD) scores Molecular Genetics and Metabolism ·M. Carmen López Castillo,吴韶红,Serwet Demirdas,Hidde H. Huidekoper,Janneke G. Langendonk,Martina Wilke,Chengzhi Xu,Henk J. Blom,Marcel Reinders,George J. G. Ruijter	2022	4
6	De novo TRPV4 Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathy Journal of Medical Genetics ·A. Goicoa,Carolina Cavaliéri Gomes,Karen Bindels‐de Heus,Renata Lazari Sandoval,Angelia V. Bassenden,Luciano Lauria Dib,Fernando Kok,Michèle RIMASSON,Irene M.J. Mathijssen,Ángel Emigdio Lagarda Lagarda,Robert Eveleigh,Tenzin Gayden,Bas Pullens,Albert M. Berghuis,Marjon van Slegtenhorst,Martina Wilke,Nada Jabado,Grazia M.S. Mancini,Ricardo Santiago Gomez	2021	9
7	Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist European Journal of Paediatric Neurology ·Grazia M.S. Mancini,Daphne J. Smits,I. Igelerud,Rachel Schot,Marie‐Claire Y. de Wit,Maarten H. Lequin,Marjolein H. G. Dremmen,Alice S. Brooks,Tjakko J. van Ham,Frans W. Verheijen,Maarten Fornerod,William B. Dobyns,Martina Wilke	2021	1
8	Meiotic arrest occurs most frequently at metaphase and is often incomplete in azoospermic men Fertility and Sterility ·Yasser Sultan,Esther Sleddens–Linkels,Marja Ooms,D Wang,Martina Wilke,Eric Blom,Gert R. Dohle,Leendert H. J. Looijenga,Wiggert A. van Cappellen,Esther B. Baart,Willy M. Baarends	2019	13
9	Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis European Journal of Medical Genetics ·PA ARRUDA MELLO,Rachel Schot,A. Jeannette M. Hoogeboom,Carsten R. Lincke,I.F.M. de Coo,Maarten H. Lequin,Marjolein H. G. Dremmen,Leontine van Unen,Jasper J. Saris,Anna Jansen,Marjon A. van Slegtenhorst,Martina Wilke,Grazia M.S. Mancini	2018	7
10	Rescue of Murine F508del CFTR Activity in Native Intestine by Low Temperature and Proteasome Inhibitors PLoS ONE ·Martina Wilke,Alice G.M. Bot,Huub Jorna,Bob J. Scholte,Hugo R. de Jonge	2012	20
11	Combined functional and causal connectivity analyses of language networks in children: A feasibility study Brain and Language ·Martina Wilke,Karen Lidzba,I Krägeloh-Mann	2008	19
12	Parallel Improvement of Sodium and Chloride Transport Defects by Miglustat (n-Butyldeoxynojyrimicin) in Cystic Fibrosis Epithelial Cells Journal of Pharmacology and Experimental Therapeutics ·Sabrina Noël,Martina Wilke,Alice G.M. Bot,Hugo R. de Jonge,Frédéric Becq	2008	40
13	Stimulation of salivary secretion in vivo by CFTR potentiators in Cftr+/+ and Cftr−/− mice Journal of Cystic Fibrosis ·Sabrina Noël,Pierre‐Olivier Strale,Luc Dannhoffer,Martina Wilke,Wiesław Trampczyńsf,由美子中本,Yvette Mettey,Frédéric Becq	2007	14
14	Spontaneous rescue from cystic fibrosis in a mouse model BMC Genetics ·Jing Genping,Martina Wilke,Martina Dorsch,Alice G.M. Bot,Huub Jorna,健渋谷,Frauke Stanke,Hans J. Hedrich,Hugo R. de Jonge,Burkhard Tümmler	2006	23
15	Rescue of functional delF508‐CFTR channels in cystic fibrosis epithelial cells by the α‐glucosidase inhibitor miglustat FEBS Letters ·Caroline Norez,Sabrina Noël,Martina Wilke,Marcel J. C. Bijvelds,Huub Jorna,Patricia Melin,Wiesław Trampczyńsf,Frédéric Becq	2006	113
16	Quantification of the HA-1 gene product at the RNA level; relevance for immunotherapy of hematological malignancies The Hematology Journal ·Martina Wilke,Harry Dolstra,Frans Maas,Jos Pool,Rolf E. Brouwer,JH Falkenburg,Pilar Bachiller,Femke Lamers,Ed Schuuring,Philip M. Kluin,Francis Brasseur,Els Goulmy	2003	32
17	The Hematopoietic System–specific Minor Histocompatibility Antigen HA-1 Shows Aberrant Expression in Epithelial Cancer Cells The Journal of Experimental Medicine ·Christoph A. Klein,Martina Wilke,Jos Pool,Maria HT Cologna,Els Blokland,Elke Burghart,Aging Liver,ARNE BARKHEM,Bernward Passlick,Alfred Stobbe,Els Goulmy	2002	67
18	Efficient induction of minor histocompatibility antigen HA-1-specific cytotoxic T-cells using dendritic cells retrovirally transduced with HA-1-coding cDNA Biology of Blood and Marrow Transplantation ·Tuna Mutis,Kamran Ghoreschi,Ellen Schrama,Janine Kamp,Mirjam H.M. Heemskerk,JH Falkenburg,Martina Wilke,Els Goulmy	2002	30
19	Exclusive TCRVβ chain usage of ex vivo generated minor Histocompatibility antigen HA-1 specific cytotoxic T cells: implications for monitoring of immunotherapy of leukemia by TCRBV spectratyping The Hematology Journal ·Robert M. Verdijk,Tuna Mutis,Martina Wilke,Jos Pool,Ellen Schrama,Anneke Brand,Els Goulmy	2002	15
20	The HA-2 Minor Histocompatibility Antigen Is Derived from a Diallelic Gene Encoding a Novel Human Class I Myosin Protein The Journal of Immunology ·Richard A. Pierce,Niteesh Potu,Tuna Mutis,Tatiana N. Golovina,C. Von Kap-Herr,Martina Wilke,Jos Pool,Jeffrey Shabanowitz,Mark J. Pettenati,Laurence C. Eisenlohr,Donald F. Hunt,Els Goulmy,Víctor H. Engelhard	2001	97

About Martina Wilke

Martina Wilke is a scholar working on Immunology, Pulmonary and Respiratory Medicine and General Decision Sciences, having authored 52 papers that have together received 1.6k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (17 papers), Immunotherapy and Immune Responses (8 papers), T-cell and B-cell Immunology (8 papers), Neonatal Respiratory Health Research (7 papers), Immune Cell Function and Interaction (6 papers), Genomics and Rare Diseases (5 papers), Hematopoietic Stem Cell Transplantation (5 papers) and Congenital heart defects research (4 papers). The work is most often cited by research in Hematology (217 citations), Pulmonary and Respiratory Medicine (580 citations) and Immunology (372 citations). Martina Wilke has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Bob J. Scholte, Hugo R. de Jonge, Huub Jorna, Els Goulmy, Alice G.M. Bot, Elisabetta Fortunati, Frédéric Becq, Sabrina Noël, Jamil Aarbiou and William H Colledge. Their work appears in journals such as Journal of Cystic Fibrosis, European Journal of Medical Genetics, American Journal of Physiology-Lung Cellular and Molecular Physiology, The Hematology Journal and BMC Genetics.

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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