Bader Alhaddad

2.3k citations

29 papers · 516 indexed · h-index 15

Co-authors: Tobias B. Haack Thomas Meitinger Tim M. Strom Wasim Ahmad Muhammad Umair Holger Prokisch Katharina Vill Elisabeth Graf
Topics: Genomics and Rare Diseases (6 papers)Metabolism and Genetic Disorders (6 papers)Neurological diseases and metabolism (5 papers)
Cited by: Developmental Biology Clinical Biochemistry Genetics
Journals: Brain The American Journal of Human Genetics Journal of Medical Genetics
Partner nations: Germany Netherlands Austria

In The Last Decade

Bader Alhaddad

29 papers receiving 513 citations

Peers

Countries citing papers authored by Bader Alhaddad

Since Specialization

Citations

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

Fields of papers citing papers by Bader Alhaddad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bader Alhaddad

This figure shows the co-authorship network connecting the top 25 collaborators of Bader Alhaddad. A scholar is included among the top collaborators of Bader Alhaddad based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bader Alhaddad. Bader Alhaddad is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Reclassifying variations of unknown significance in diseases affecting Saudi Arabia’s population reveal new associations 2023 ·Frontiers in Genetics ·(unknown),(unknown),Bader Alhaddad,(unknown),(unknown),(unknown),Mohamed Abouelhoda,(unknown)	3
2	Prospect of genetic disorders in Saudi Arabia 2023 ·Frontiers in Genetics ·(unknown),(unknown),(unknown),(unknown),(unknown),Ahmed Alfares,Bader Alhaddad,(unknown)	7
3	Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystonia 2020 ·Parkinsonism & Related Disorders ·Michael Zech,Theresa Brunet,Matěj Škorvánek,Astrid Blaschek,Katharina Vill,(unknown),Irina Hüning,Vladimír Haň,(unknown),Zuzana Gdovinová,Bader Alhaddad,Riccardo Berutti,Tim M. Strom,Evžen Růžička,Erik‐Jan Kamsteeg,Jasper J. van der Smagt,Matias Wagner,Robert Jech,Juliane Winkelmann	4
4	Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGS 2020 ·European Journal of Human Genetics ·Matthias C. Braunisch,Korbinian M. Riedhammer,(unknown),(unknown),Roman Günthner,Matias Wagner,Marc Weidenbusch,Adrian Lungu,Bader Alhaddad,Lutz Renders,Tim M. Strom,Uwe Heemann,Thomas Meitinger,Christoph Schmaderer,Julia Hoefele	11
5	LINS1 -associated neurodevelopmental disorder 2020 ·Neurology Genetics ·Christiane Neuhofer,Claudia B. Catarino,Heinrich Schmidt,Klaus Seelos,Bader Alhaddad,Tobias B. Haack,Thomas Klopstock	4
6	Whole‐exome sequencing revealed a nonsense mutation in STKLD1 causing non‐syndromic pre‐axial polydactyly type A affecting only upper limb 2019 ·Clinical Genetics ·Muhammad Umair,Muhammad Bilal,Raja Hussain Ali,Bader Alhaddad,Farooq Ahmad,Abdullah Abdullah,Tobias B. Haack,Majid Alfadhel,Muhammad Ansar,Thomas Meitinger,Wasim Ahmad	8
7	A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic Encephalopathy 2018 ·JIMD Reports ·Arcangela Iuso,Bader Alhaddad,(unknown),Urania Kotzaeridou,Elisa Mastantuono,Thomas Schwarzmayr,Elisabeth Graf,Caterina Terrile,Holger Prokisch,Tim M. Strom,Georg F. Hoffmann,Thomas Meitinger,Tobias B. Haack	19
8	KIF16B is a candidate gene for a novel autosomal‐recessive intellectual disability syndrome 2018 ·American Journal of Medical Genetics Part A ·Saud Alsahli,Stefan T. Arold,Ahmed Alfares,Bader Alhaddad,Mohammed Al Balwi,Erik‐Jan Kamsteeg,Waleed Altwaijri,Majid Alfadhel	7
9	Severe ichthyosis in MPDU1‐CDG 2018 ·Journal of Inherited Metabolic Disease ·Christian Thiel,Saskia B. Wortmann,Korbinian M. Riedhammer,Bader Alhaddad,Ertan Mayatepek,Holger Prokisch,Felix Dıstelmaıer	9
10	Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies 2017 ·Oxidative Medicine and Cellular Longevity ·René G. Feichtinger,Michaela Brunner‐Krainz,Bader Alhaddad,Saskia B. Wortmann,Réka Kovács-Nagy,Tatjana Stojaković,Wolfgang Erwa,Bernhard Resch,Werner Windischhofer,(unknown),Sabine Uhrig,Christian Windpassinger,Felix Sternberg,Christine Makowski,Tim M. Strom,Thomas Meitinger,Holger Prokisch,Wolfgang Sperl,Tobias B. Haack,Johannes A. Mayr	33
11	Identification of a Novel Heterozygous De Novo 7-bp Frameshift Deletion in PBX1 by Whole-Exome Sequencing Causing a Multi-Organ Syndrome Including Bilateral Dysplastic Kidneys and Hypoplastic Clavicles 2017 ·Frontiers in Pediatrics ·Korbinian M. Riedhammer,Corinna Siegel,Bader Alhaddad,Carmen Montoya,Réka Kovács-Nagy,Matias Wagner,Thomas Meitinger,Julia Hoefele	15
12	LYRM7 - associated complex III deficiency: A clinical, molecular genetic, MR tomographic, and biochemical study 2017 ·Mitochondrion ·Maja Hempel,Laura S. Kremer,Konstantinos Tsiakas,Bader Alhaddad,Tobias B. Haack,Ulrike Löbel,René G. Feichtinger,Wolfgang Sperl,Holger Prokisch,Johannes A. Mayr,René Santer	18
13	Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3 2017 ·Pediatric Research ·Muhammad Umair,Bader Alhaddad,(unknown),(unknown),Tobias B. Haack,Elisabeth Graf,Asmat Ullah,Farooq Ahmad,Tim M. Strom,Thomas Meitinger,Wasim Ahmad	26
14	Ellis–van Creveld syndrome and profound deafness resulted by sequence variants in the EVC / EVC2 and TMC1 genes 2017 ·Journal of Genetics ·Muhammad Umair,Heide Seidel,(unknown),Asmat Ullah,Tobias B. Haack,Bader Alhaddad,(unknown),(unknown),Tim M. Strom,Farooq Ahmad,Thomas Meitinger,Wasim Ahmad	20
15	Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalities 2017 ·European Journal of Human Genetics ·Diran Herebıan,Bader Alhaddad,Annette Seibt,Thomas Schwarzmayr,Katharina Danhauser,Dirk Klee,(unknown),Thomas Meitinger,Tim M. Strom,Ansgar Schulz,Ertan Mayatepek,Tobias B. Haack,Felix Dıstelmaıer	11
16	Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb 2017 ·European Journal of Human Genetics ·Muhammad Umair,Khadim Shah,Bader Alhaddad,Tobias B. Haack,Elisabeth Graf,Tim M. Strom,Thomas Meitinger,Wasim Ahmad	36
17	Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia 2016 ·The American Journal of Human Genetics ·Michael Zech,Sylvia Boesch,Esther M. Maier,Ingo Borggraefe,Katharina Vill,Franco Laccone,Veronika Pilshofer,Andrés Ceballos-Baumann,Bader Alhaddad,Riccardo Berutti,Werner Poewe,Tobias B. Haack,Bernhard Haslinger,Tim M. Strom,Juliane Winkelmann	99
18	EARS2 mutations cause fatal neonatal lactic acidosis, recurrent hypoglycemia and agenesis of corpus callosum 2016 ·Metabolic Brain Disease ·Katharina Danhauser,Tobias B. Haack,Bader Alhaddad,(unknown),Annette Seibt,Tim M. Strom,Thomas Meitinger,Dirk Klee,Ertan Mayatepek,Holger Prokisch,Felix Distelmaier	12
19	A new missense mutation in UMOD gene leads to severely reduced serum uromodulin concentrations — A tool for the diagnosis of uromodulin-associated kidney disease 2016 ·Clinical Biochemistry ·Robin Satanovskij,Bader Alhaddad,Matthias Block,Victor Herbst,Wolfgang Schlumberger,Tobias B. Haack,Wolfgang Andreas Nockher,Uwe Heemann,Lutz Renders,Christoph Schmaderer,Susanne Angermann,Ming Wen,Thomas Meitinger,Jürgen E. Scherberich,Dominik Steubl	12
20	Neonatal encephalocardiomyopathy caused by mutations in VARS2 2016 ·Metabolic Brain Disease ·Fabian Baertling,Bader Alhaddad,Annette Seibt,(unknown),Thomas Meitinger,Tim M. Strom,Ertan Mayatepek,Jörg Schaper,Holger Prokisch,Tobias B. Haack,Felix Dıstelmaıer	21

About Bader Alhaddad

Bader Alhaddad is a scholar working on Developmental Biology, Clinical Biochemistry and Neurology, having authored 29 papers that have together received 516 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Metabolism and Genetic Disorders (6 papers) and Neurological diseases and metabolism (5 papers). The work is most often cited by research in Developmental Biology (46 citations), Clinical Biochemistry (89 citations) and Genetics (174 citations). Bader Alhaddad has collaborated with scholars based in Germany, Netherlands and Austria. Frequent co-authors include Tobias B. Haack, Thomas Meitinger, Tim M. Strom, Wasim Ahmad, Muhammad Umair, Holger Prokisch, Katharina Vill, Elisabeth Graf, Bernhard Haslinger and Ingo Borggraefe. Their work appears in journals such as Brain, The American Journal of Human Genetics and Journal of Medical 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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