Abdul Noor

8.0k total citations
42 papers, 1.4k citations indexed

About

Abdul Noor is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Abdul Noor has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 17 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Abdul Noor's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (8 papers). Abdul Noor is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (8 papers). Abdul Noor collaborates with scholars based in Canada, United Kingdom and Malaysia. Abdul Noor's co-authors include John B. Vincent, Christian Windpassinger, Muhammad Ayub, D. D. Wood, Mario A. Moscarello, Fabrizio G. Mastronardi, Tara Paton, Stephen W. Scherer, Muhammad Rafiq and Anath C. Lionel and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Schizophrenia Research.

In The Last Decade

Abdul Noor

41 papers receiving 1.4k citations

Peers

Countries citing papers authored by Abdul Noor

Since Specialization

Citations

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

Fields of papers citing papers by Abdul Noor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdul Noor

This figure shows the co-authorship network connecting the top 25 collaborators of Abdul Noor. A scholar is included among the top collaborators of Abdul Noor 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 Abdul Noor. Abdul Noor 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	Validation of low‐pass genome sequencing for prenatal diagnosis 2024 ·Prenatal Diagnosis ·Chloe Mighton, Abdul Noor, Nicholas A. Watkins, (unknown), Jordan Lerner‐Ellis, Andrew Wong, (unknown), (unknown), David Chitayat, (unknown)	3
2	Role of comprehensive cytogenomic investigation in successful reproductive outcome of parental small neocentromeric supernumerary ring chromosome: A case report 2023 ·SHILAP Revista de lepidopterología ·Yiming Wang, Joanna Lazier, (unknown), Abdul Noor, David Chitayat, (unknown)	2
3	Androgenetic/Biparental Mosaic/Chimeric Conceptions With a Molar Component: A Diagnostic and Clinical Challenge 2020 ·International Journal of Gynecological Pathology ·Anjelica Hodgson, Valérie Dubé, Sarah Strickland, Elena Kolomietz, Abdul Noor, (unknown), Terence J. Colgan, Gulisa Turashvili	4
4	Molecular Diagnosis of Placental Hydatidiform Mole: Innovation and Outcomes 2017 ·Journal of Obstetrics and Gynaecology Canada ·Terence J. Colgan, Abdul Noor, (unknown), Martin C. Chang, Elena Kolomietz	5
5	Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia 2017 ·Genome Medicine ·Chelsea Lowther, Daniele Merico, Gregory Costain, (unknown), Kerry Boyd, Abdul Noor, Marsha Speevak, Dimitri J. Stavropoulos, John Wei, Anath C. Lionel, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett	24
6	Case Report: Use of Tumor and Germline Y Chromosomal Analysis to Guide Surgical Management in a 46, XX Female Presenting With Gonadoblastoma With Dysgerminoma 2016 ·International Journal of Gynecological Pathology ·Jeanna McCuaig, Abdul Noor, Barry P. Rosen, Robert F. Casper, (unknown), Terence J. Colgan, Raymond H. Kim	4
7	Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families 2014 ·Neurogenetics ·(unknown), Katharina M. Roetzer, Abdul Noor, Anath C. Lionel, (unknown), Thomas Schwarzbraun, (unknown), Anna Mikhailov, Christian R. Marshall, Christian Windpassinger, Erwin Petek, Stephen W. Scherer, Wolfgang Kaschnitz, John B. Vincent	90
8	Broadening the ciliopathy spectrum: Motile cilia dyskinesia, and nephronophthisis associated with a previously unreported homozygous mutation in the INVS/NPHP2 gene 2013 ·American Journal of Medical Genetics Part A ·Sharon Moalem, Sarah Keating, Patrick Shannon, Megan Thompson, (unknown), Keith Nykamp, (unknown), Abdul Noor, David Chitayat	21
9	Osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region Xq11.2 2012 ·American Journal of Medical Genetics Part A ·Sébastien Chénier, Abdul Noor, Lucie Dupuis, Dimitri J. Stavropoulos, Roberto Mendoza‐Londono	10
10	Evaluation of medical students’ perception towards the BigSib Programme in the School of Medical Sciences, USM 2010 ·Education in Medicine Journal ·Muhamad Saiful Bahri Yusoff, Ahmad Fuad Abdul Rahim, Abdul Noor, Nor Azwany Yaacob, Zabidi Azhar Mohd Hussin	11
11	Evaluation of medical students’ perception towards the BigSib programme in the School of Medical Sciences, Universiti Sains Malaysia 2010 ·Education in Medicine Journal ·Muhamad Saiful Bahri Yusoff, Ahmad Fuad Abdul Rahim, Abdul Noor, Nor Azwany Yaacob, Zabidi Azhar Mohd Hussin	5
12	Mapping of three novel loci for non‐syndromic autosomal recessive mental retardation (NS‐ARMR) in consanguineous families from Pakistan 2010 ·Clinical Genetics ·(unknown), Muhammad Ansar, (unknown), Abdul Noor, (unknown), (unknown), (unknown), (unknown), Muhammad Aminuddin, Lars Feuk, (unknown), Stephen W. Scherer	13
13	Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3 2009 ·The American Journal of Human Genetics ·Abdul Noor, Christian Windpassinger, Irina Vitcu, M Orlic-Milacic, Muhammad Rafiq, (unknown), (unknown), Muhammad Ayub, Benjamin A. Alman, John B. Vincent	65
14	Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation 2009 ·The American Journal of Human Genetics ·Asif Mir, (unknown), Abdul Noor, M. Mahdi Motazacker, (unknown), Matloob Azam, Kimia Kahrizi, Muhammad Rafiq, (unknown), (unknown), Farooq Naeem, Andreas Tzschach, Andreas W. Kuß, Gisele E. Ishak, Dan Doherty, Hans‐Hilger Ropers, A. James Barkovich, Hossein Najmabadi, Muhammad Ayub, John B. Vincent	97
15	Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close toSH3TC2,ADRB2, andHTR4on 5q, and within the desmocollin gene cluster on 18q 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·John B. Vincent, Abdul Noor, Christian Windpassinger, Peter J. Gianakopoulos, Thomas Schwarzbraun, Simon E. Alfred, (unknown), Stephen W. Scherer, Wendy Roberts, Klaus Wagner, Peter M. Kroisel, Erwin Petek	11
16	Sequence variants within exon 1 of MECP2 occur in females with mental retardation 2006 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown), (unknown), (unknown), Abdul Noor, (unknown), (unknown), Gevork N. Mnatzakanian, Simon E. Alfred, (unknown), Stephen W. Scherer, James L. Kennedy, Wendy Roberts, (unknown), (unknown), John B. Vincent	19
17	Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome 2006 ·Molecular Genetics and Genomics ·Erwin Petek, Thomas Schwarzbraun, Abdul Noor, Megha Patel, Kazuhiko Nakabayashi, Sanaa Choufani, Christian Windpassinger, M. Stamenković, Mary M. Robertson, H.N. Aschauer, Hugh Gurling, Peter M. Kroisel, Klaus Wagner, Stephen W. Scherer, John B. Vincent	46
18	EFFECT OF FLUOXETINE ON MAXIMAL ELECTROSHOCK SEIZURES IN MICE: ACUTE VS CHRONIC ADMINISTRATION 1999 ·Pharmacological Research ·(unknown), Abdul Noor, (unknown), (unknown), (unknown), Heng Chin Low, (unknown)	32
19	Laryngeal paralysis in organophosphorous poisoning 1998 ·The Journal of Laryngology & Otology ·(unknown), (unknown), Abdul Noor	12
20	Blood pressure regulation by the kallikrein-kinin system 1996 ·General Pharmacology The Vascular System ·J. N. Sharma, (unknown), Abdul Noor, (unknown)	45

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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