Fahed Halal

1.7k citations

50 papers · 1.2k indexed · h-index 18

Developmental Biology top 5%
- Congenital limb and hand anomalies 11
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 4
- Genetic Syndromes and Imprinting 3
- Genomics and Rare Diseases 3
- Connective tissue disorders research 3
Genetics top 10%
- Neurogenetic and Muscular Disorders Research 4
- Genetic Syndromes and Imprinting 3
- Genomics and Rare Diseases 3
- Connective tissue disorders research 3
Pediatrics, Perinatology and Child Health top 10%
Surgery top 10%
Urology
- Urological Disorders and Treatments 8
Molecular Biology
- Congenital heart defects research 4
- Hedgehog Signaling Pathway Studies 3

Co-authors: John M. Opitz F. Clarke Fraser John M. Optiz Vazken M. Der Kaloustian D. Ross McLeod Stephen R. Williams Helga V. Toriello Robert B. Gledhill
Cited by: Developmental Biology Genetics Pediatrics, Perinatology and Child Health
Journals: American Journal of Medical Genetics (36 papers)The American Journal of Human Genetics (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: Canada United States Syria

In The Last Decade

Fahed Halal

49 papers receiving 1.1k citations

Peers

Countries citing papers authored by Fahed Halal

Since Specialization

Citations

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

Fields of papers citing papers by Fahed Halal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Prevalence of hypomineralised second primary molars (HSPM) in Syrian preschool children European Archives of Paediatric Dentistry ·Fahed Halal,Nandang Bekti Karnowati	2020	7
2	Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations European Journal of Human Genetics ·Nataliya Di Donato,Andreas Rump,Rainer Koenig,Vazken M. Der Kaloustian,Fahed Halal,K. Sonntag,Crystal Krause,Karl Hackmann,Gabriele Hahn,Evelin Schröck,Alain Verloès	2013	59
3	Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems The American Journal of Human Genetics ·Stephen R. Williams,Micheala A. Aldred,Vazken M. Der Kaloustian,Fahed Halal,Gordon C. Gowans,D. Ross McLeod,Kalpika M.,Helga V. Toriello,R. Ellen Magenis,Sarah H. Elsea	2010	216
4	Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: A new syndrome? American Journal of Medical Genetics ·Claudia Evers,Daniela Cristina Valea,Heather J. Stalker,Z Weng,Aurore Côté,Fahed Halal	1993	10
5	Ring chromosome 20 and possible assignment of the structural gene encoding human carboxypeptidase‐L to the distal segment of the long arm of chromosome 20 American Journal of Medical Genetics ·Fahed Halal,David Chitayat,Stephen J. Lestrange,Bernard Rosenblatt,Floris C. Freeman,Michel Vekemans,Michel Potier	1992	9
6	Syndrome of microcephaly, Brachmann–de Lange‐like facial changes, severe metatarsus adductus, and developmental delay: Mild Brachmann‐de Lange syndrome? American Journal of Medical Genetics ·Fahed Halal,Kenneth Silver	1992	14
7	Interstitial tandem direct duplication of the long arm of chromosome 4 (q23‐q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segment American Journal of Medical Genetics ·Fahed Halal,Michel Vekemans,David Chitayat	1991	19
8	Generalized enchondromatosis in a boy with only platyspondyly in the father American Journal of Medical Genetics ·Fahed Halal,E. Michel Azouz	1991	29
9	Distal deletion of chromosome 1q in an adult American Journal of Medical Genetics ·Fahed Halal,Michel Vekemans,Paige Kaplan,Lidia van Driel-Gesztelyi	1990	15
10	The syndrome of hirschsprung disease, microcephaly, unusual face, and mental retardation American Journal of Medical Genetics ·Fahed Halal,T. A. S. SOUTO	1990	19
11	Ring chromosome 4 in a child with duodenal atresia American Journal of Medical Genetics ·Fahed Halal,Michel Vekemans	1990	10
12	Slowly progressive macrocephaly with hamartomas: A new syndrome? American Journal of Medical Genetics ·Fahed Halal,Kenneth Silver	1989	14
13	A presumptive translocation 1p;2q resulting in duplication 1p and deletion 2q American Journal of Medical Genetics ·Fahed Halal,Michel Vekemans,Vazken M. Der Kaloustian	1989	10
14	Autosomal dominant inheritance of the Kabuki make‐up (Niikawa‐Kuroki) syndrome American Journal of Medical Genetics ·Fahed Halal,Robert B. Gledhill,Isabelle Chanu	1989	65
15	The Hand‐Foot‐Genital (Hand‐Foot‐Uterus) syndrome: Family report and update American Journal of Medical Genetics ·Fahed Halal,John M. Opitz,James F. Reynolds	1988	27
16	Ruvalcaba‐Myhre‐Smith Syndrome Pediatric Dermatology ·輝夫平田,D. Medina Zambrano,Lawrence S. Shachner,John H. DiLiberti,Rogelio H.A. Ruvalcaba,Bhoknal Kavita B,Richard G. Weleber,Fahed Halal,Mark Lipson,Bruce Blumberg,Paul J. Weber	1988	12
17	Intracranial aneurysms: A report of a large pedigree American Journal of Medical Genetics ·Fahed Halal,Gérard Mohr,Luo Yue-ji,Haiyan Zhu	1983	19
18	Male to male transmission of cerebral gigantism American Journal of Medical Genetics ·Fahed Halal	1982	33
19	Acro‐renal‐mandibular syndrome American Journal of Medical Genetics ·Fahed Halal,A. L. Glusko,Bernard Leduc,Karen A. Autio,剛阪上	1980	26
20	Camptodactyly, cleft palate, and club foot (the Gordon syndrome). A report of a large pedigree. Journal of Medical Genetics ·Fahed Halal,F C Fraser	1979	17

About Fahed Halal

Fahed Halal is a scholar working on Developmental Biology, Urology, Genetics, Genetics and Rheumatology, having authored 50 papers that have together received 1.2k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (11 papers), Urological Disorders and Treatments (8 papers), Congenital heart defects research (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Genetic Syndromes and Imprinting (3 papers), Genomics and Rare Diseases (3 papers), Connective tissue disorders research (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). The work is most often cited by research in Developmental Biology (82 citations), Genetics (564 citations), Genetics (98 citations), Pediatrics, Perinatology and Child Health (151 citations) and Surgery (332 citations). Fahed Halal has collaborated with scholars based in Canada, United States and Syria. Frequent co-authors include John M. Opitz, F. Clarke Fraser, John M. Optiz, Vazken M. Der Kaloustian, D. Ross McLeod, Stephen R. Williams, Helga V. Toriello, Robert B. Gledhill, Micheala A. Aldred and Gordon C. Gowans. Their work appears in journals such as American Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Human Genetics, European Archives of Paediatric Dentistry and Pediatric Dermatology.

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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