Alexander P.A. Stegmann

7.0k citations

52 papers · 2.0k indexed · h-index 24

Immunology top 5%
- T-cell and B-cell Immunology 5
Transplantation top 5%
Genetics top 5%
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 6
- Chronic Lymphocytic Leukemia Research 4
Oncology top 10%
Hematology top 5%
- Acute Myeloid Leukemia Research 5
Molecular Biology
- Congenital heart defects research 5
Surgery
- Transplantation: Methods and Outcomes 5

Co-authors: Hergen Spits Arjen Q. Bakker Kees Weijer Bianca Blom Mirjam H.M. Heemskerk Beverly S. Mitchell Fiona M. Smart J. E. Landegent
Cited by: Immunology Transplantation Genetics
Journals: European Journal of Medical Genetics (4 papers)Journal of Clinical Investigation (2 papers)Clinical Genetics (2 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Alexander P.A. Stegmann

49 papers receiving 2.0k citations

Peers

Countries citing papers authored by Alexander P.A. Stegmann

Since Specialization

Citations

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

Fields of papers citing papers by Alexander P.A. Stegmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander P.A. Stegmann. 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 Alexander P.A. Stegmann. The network helps show where Alexander P.A. Stegmann may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation Nature Communications ·Wouter Steyaert,Lonneke Haer‐Wigman,Rolph Pfundt,Debby M.E.I. Hellebrekers,Marloes Steehouwer,A Castellanos Guerrero,Elke de Boer,Alexander P.A. Stegmann,Helger G. Yntema,Erik‐Jan Kamsteeg,Han G. Brunner,Alexander Hoischen,Christian Gilissen	2023	5
2	Monoallelic CRMP1 gene variants cause neurodevelopmental disorder eLife ·Paul J. Limburg,Nobuto Arashiki,Lena‐Luise Becker,Gerald Gifford,Jonathan Lévy,Thomas Rambaud,Ching Chuan Low,Yoshio Goshima,Na Li,Maaike Vreeburg,Bénédicte Demeer,Achim Dickmanns,Alexander P.A. Stegmann,Hao Hu,Fumio Nakamura,Angela M. Kaindl	2022	5
3	Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice Genetics in Medicine ·Suzanne C.E.H. Sallevelt,Alexander P.A. Stegmann,Bart de Koning,W. Setya,Anja Steyls,Fu,Phillis Lakeman,Helger G. Yntema,Masoud Zamani Esteki,Christine de Die‐Smulders,Christian Gilissen,Arthur van den Wijngaard,Han G. Brunner,Aimée Paulussen	2021	26
4	The adult phenotype of Schaaf-Yang syndrome Orphanet Journal of Rare Diseases ·A Klamert,Magdeldin Elgizouli,Fatoumatta L. Kassama,Jasmin Beygo,Florian Erger,N. M. Alloush,Constance T. R. M. Stumpel,Alexander P.A. Stegmann,Stefanie Beck‐Wödl,Gabriele Gillessen‐Kaesbach,Bernhard Horsthemke,Christian P. Schaaf,Alma Kuechler	2020	19
5	Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability Epilepsia ·Francesca M. Snoeijen‐Schouwenaars,Iliana Castro Liera,Judith Verhoeven,Petra van Mierlo,Hilde M. H. Braakman,Eric Smeets,Joost Nicolai,Jeroen Schoots,辻村昌希,Rob P.W. Rouhl,Francis Tan,Helger G. Yntema,Han G. Brunner,Rolph Pfundt,Alexander P.A. Stegmann,Erik‐Jan Kamsteeg,Helenius J. Schelhaas,Marjolein H. Willemsen	2018	60
6	Cutaneous clues for diagnosing X‐chromosomal disorders Clinical Genetics ·Maaike Vreeburg,Suzanne C.E.H. Sallevelt,Alexander P.A. Stegmann,Michel van Geel,Box La,C. T. R. M. Schrander‐Stumpel,Maurice A. M. Van Steensel,寺島薫	2013	1
7	SAMS, a Syndrome of Short Stature, Auditory-Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Is a Unique Neurocristopathy Caused by Mutations in Goosecoid The American Journal of Human Genetics ·David Parry,Clare V. Logan,Alexander P.A. Stegmann,Zakia A. Abdelhamed,Alistair Calder,Mbuotidem Udongwo,David T. Bonthron,Virginia Clowes,Eamonn Sheridan,Neeti Ghali,Albert E. Chudley,Angus Dobbie,Constance T. R. M. Stumpel,Colin A. Johnson	2013	27
8	Adducted thumbs: A clinical clue to genetic diagnosis European Journal of Medical Genetics ·Judith M.A. Verhagen,C. T. R. M. Schrander‐Stumpel,Choristers of Worcester Cathedra,Jacobiene W. Weber,J. J. P. Schrander,M. Estela Rubio‐Gozalbo,Jaap Bakker,Alexander P.A. Stegmann,Yvonne J. Vos,Suzanna G.M. Frints	2012	9
9	Defective NDUFA9 as a novel cause of neonatally fatal complex I disease Journal of Medical Genetics ·B.J.C. van den Bosch,Mike Gerards,Wim J. Sluiter,Alexander P.A. Stegmann,祥一仲村,Debby M.E.I. Hellebrekers,Renske Oegema,Solomia Jebessa Deribessa,Holger Prokisch,Katharina Danhauser,Kees Schoonderwoerd,I.F.M. de Coo,Hubert J.M. Smeets	2011	46
10	Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy–Walker malformation American Journal of Medical Genetics Part A ·Maurice A. M. Van Steensel,Maaike Vreeburg,Jan Engelen,Marcus Garbe,Alexander P.A. Stegmann,J. Herbergs,J.W.M. van Lent,H.J.M. Smeets,Yung Zu Park	2008	21
11	Prospective screening of patients with unexplained mental retardation using subtelomeric MLPA strongly increases the detection rate of cryptic unbalanced chromosomal rearrangements European Journal of Medical Genetics ·Alexander P.A. Stegmann,K. Kernisant,J.J.M. Engelen	2007	14
12	Immunological aspects of fresh and cryopreserved aortic valve transplantation in rats The Annals of Thoracic Surgery ·Frans B S Oei,Alexander P.A. Stegmann,C Manoj,Richard L. Marquet,Willem Weimar,Ad J.J.C. Bogers	2001	19
13	Inhibition of T lymphocyte activation in mice heterozygous for loss of the IMPDH II gene Journal of Clinical Investigation ·Jing Gu,Alexander P.A. Stegmann,Karen Gathy,Robert Murray,Boris Po-Tsang Chen,Lanier H. Ayscue,Beverly S. Mitchell	2000	60
14	Pharmacological analysis of contractile effects of eletriptan and sumatriptan on human isolated blood vessels European Journal of Pharmacology ·Luděk Šarman,Antoinette MaassenVanDenBrink,René de Vries,Ad J.J.C. Bogers,Alexander P.A. Stegmann,C. J. J. Avezaat,Pramod R. Saxena	2000	32
15	Circulating donor-specific cytotoxic T lymphocytes with high avidity for donor human leukocyte antigens in pediatric and adult cardiac allograft valved conduit recipients✩ European Journal of Cardio-Thoracic Surgery ·Frans B S Oei,Marij J.P. Welters,Azhar Tanjung Azhar Tanjung,L. M. B. Vaessen,Alexander P.A. Stegmann,Willem Weimar,Ad J.J.C. Bogers	2000	18
16	Distinct Roles of the Phosphatidylinositol 3-Kinase and STAT5 Pathways in IL-7-Mediated Development of Human Thymocyte Precursors Immunity ·Alois M. Carnier,Alexander P.A. Stegmann,R. Rocha,Fiona M. Smart,Ashok R. Venkitaraman,Hergen Spits	1999	172
17	Disruption of αβ but not of γδ T cell development by overexpression of the helix–loop–helix protein Id3 in committed T cell progenitors The EMBO Journal ·Bianca Blom,Mirjam H.M. Heemskerk,Martie C. M. Verschuren,Jacques J. M. van Dongen,Alexander P.A. Stegmann,Arjen Q. Bakker,Haixu Zhao,Hermanson Terhi,Hergen Spits	1999	82
18	Inhibition of T Cell and Promotion of Natural Killer Cell Development by the Dominant Negative Helix Loop Helix Factor Id3 The Journal of Experimental Medicine ·Mirjam H.M. Heemskerk,Bianca Blom,Garry P. Nolan,Alexander P.A. Stegmann,Arjen Q. Bakker,Kees Weijer,Hermanson Terhi,Hergen Spits	1997	232
19	In vitro-induced resistance to the deoxycytidine analogues cytarabine (AraC) and 5-aza-2′-deoxycytidine (DAC) in a rat model for acute myeloid leukemia is mediated by mutations in the deoxycytidine kinase (dck) gene Annals of Hematology ·Alexander P.A. Stegmann,M. Willy Honders,A Hagemeijer,Barbara Hoebee,R. Willemze,J. E. Landegent	1995	30
20	Assignment of the Human Deoxycytidine Kinase (DCK) Gene to Chromosome 4 Band q13.3-q21.1 Genomics ·Alexander P.A. Stegmann,M. Willy Honders,A. S. Shahab,J. Wessels,R. Willemze,J. E. Landegent	1993	8

About Alexander P.A. Stegmann

Alexander P.A. Stegmann is a scholar working on Genetics, Genetics, Transplantation, Hematology and Developmental Biology, having authored 52 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (5 papers), Transplantation: Methods and Outcomes (5 papers), Acute Myeloid Leukemia Research (5 papers), T-cell and B-cell Immunology (5 papers) and Chronic Lymphocytic Leukemia Research (4 papers). The work is most often cited by research in Immunology (598 citations), Transplantation (54 citations), Genetics (196 citations), Oncology (384 citations) and Hematology (157 citations). Alexander P.A. Stegmann has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Hergen Spits, Arjen Q. Bakker, Kees Weijer, Bianca Blom, Mirjam H.M. Heemskerk, Beverly S. Mitchell, Fiona M. Smart, J. E. Landegent, Garry P. Nolan and Ashok R. Venkitaraman. Their work appears in journals such as European Journal of Medical Genetics, Journal of Clinical Investigation, Clinical Genetics, Blood and Orphanet Journal of Rare Diseases.

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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