Marwan K. Tayeh

1.8k citations

26 papers · 1.2k indexed · h-index 15

Genetics top 5%
- Genetic Syndromes and Imprinting 8
- Genomic variations and chromosomal abnormalities 5
- Genetic and Kidney Cyst Diseases 4
- Genomics and Rare Diseases 3
Molecular Biology top 10%
- Nuclear Structure and Function 4
- Congenital heart defects research 3
- Inflammasome and immune disorders 3
Statistics and Probability top 5%
Cell Biology
Immunology
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3

Co-authors: Val C. Sheffield Edwin M. Stone Diane C. Slusarski Robert F. Mullins Hatem El‐Shanti Darryl Nishimura John S. Beck Khalil Elbedour
Cited by: Genetics Molecular Biology Statistics and Probability
Journals: Proceedings of the National Academy of Sciences (1 paper)SHILAP Revista de lepidopterología (1 paper)Blood (1 paper)
Partner nations: United States Jordan Türkiye

In The Last Decade

Marwan K. Tayeh

25 papers receiving 1.2k citations

Peers

Countries citing papers authored by Marwan K. Tayeh

Since Specialization

Citations

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

Fields of papers citing papers by Marwan K. Tayeh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marwan K. Tayeh. 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 Marwan K. Tayeh. The network helps show where Marwan K. Tayeh may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Education of Future Pharmacogenomics Laboratory Directors Reynold C. Ly,Marwan K. Tayeh,Yuan Ji	2024	1
2	Points to consider in the practice of postmortem genetic testing: A statement of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Joshua L. Deignan,Mauricio De Castro,Vanessa L. Horner,Tami Johnston,Daniela Macaya,Joseph J. Maleszewski,Honey V. Reddi,Marwan K. Tayeh	2023	6
3	Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Marwan K. Tayeh,Andrea Gaedigk,Matthew P. Goetz,Teri E. Klein,Elaine Lyon,Gwendolyn A. McMillin,Stefan Rentas,Marwan Shinawi,Victoria M. Pratt,Stuart A. Scott	2022	26
4	The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Marwan K. Tayeh,Margaret Chen,Stephanie M. Fullerton,Patrick R. Gonzales,Samuel J. Huang,Lauren Massingham,Julianne O’Daniel,Douglas R. Stewart,Ashlee R. Stiles,Barbara J. Evans	2022	4
5	Cardiac phenotype in familial partial lipodystrophy Clinical Endocrinology ·Abdelwahab Jalal Eldin,Barış Akıncı,André Monteiro da Rocha,Rasimcan Meral,İlgın Yıldırım Şimşir,Süleyman Cem Adıyaman,Ebru Özpelit,Nicole M. Bhave,Ramazan Gen,Banu Şarer Yürekli,Nilüfer Özdemir Kutbay,Zeynep Şıklar,Adam Neidert,Rita Hench,Marwan K. Tayeh,Jeffrey W. Innis,José Jalife,Hakan Oral,Elif A Oral	2021	14
6	Metreleptin therapy for nonalcoholic steatohepatitis: Open-label therapy interventions in two different clinical settings Med ·Barış Akıncı,Angela Subauste,Nevin Ajluni,Nazanene H. Esfandiari,Rasimcan Meral,Adam Neidert,Akin Eraslan,Rita Hench,Diana Rus,Barbara J. McKenna,Hero K. Hussain,Thomas L. Chenevert,Marwan K. Tayeh,Amit Rupani,Jeffrey W. Innis,Christos S. Mantzoros,Hari S. Conjeevaram,Charles Burant,Elif A Oral	2021	19
7	Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Daniela del Gaudio,Marwan Shinawi,Caroline Astbury,Marwan K. Tayeh,Kristen Deak,Gordana Raca	2020	93
8	Addendum: Technical standards and guidelines for spinal muscular atrophy testing Genetics in Medicine ·Joshua L. Deignan,Caroline Astbury,Andrea Behlmann,Saurav Guha,Kristin G. Monaghan,Honey V. Reddi,Bryce A. Seifert,Marwan K. Tayeh,Erin Wakeling	2020	3
9	Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositis SHILAP Revista de lepidopterología ·Melis Sahinoz,Shafaq Khairi,Ashley J. Cuttitta,Graham F. Brady,Amit Rupani,Rasimcan Meral,Marwan K. Tayeh,Peedikayil E. Thomas,Meredith Riebschleger,Sandra Camelo‐Piragua,Jeffrey W. Innis,M. Bishr Omary,Daniel E. Michele,Elif A Oral	2018	11
10	Spectrum of disease associated with partial lipodystrophy: lessons from a trial cohort Clinical Endocrinology ·Nevin Ajluni,Rasimcan Meral,Adam Neidert,Graham F. Brady,Eric D. Buras,Barbara J. McKenna,Frank DiPaola,Thomas L. Chenevert,Jeffrey F. Horowitz,Colleen Buggs‐Saxton,Amit Rupani,Peedikayil E. Thomas,Marwan K. Tayeh,Jeffrey W. Innis,M. Bishr Omary,Hari S. Conjeevaram,Elif A Oral	2017	73
11	Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development Congenital Heart Disease ·Thor Thorsson,William Russell,Nour El‐Kashlan,Rachel Soemedi,Jonathan M. Levine,Sarah Geisler,Todd Ackley,Aoy Tomita‐Mitchell,Jill A. Rosenfeld,Ana Töpf,Marwan K. Tayeh,Judith Goodship,Jeffrey W. Innis,Bernard Keavney,Mark W. Russell	2014	21
12	Metastatic medulloblastoma in an adolescent with Simpson–Golabi–Behmel syndrome American Journal of Medical Genetics Part A ·Martha H. Thomas,Victoria B. Enciso,Robert F. Stratton,Shafqat Shah,Thomas Winder,Marwan K. Tayeh,Elizabeth Roeder	2012	18
13	A Homozygous Mutation in ADAMTSL4 Causes Autosomal-Recessive Isolated Ectopia Lentis The American Journal of Human Genetics ·Dina Ahram,T. Shawn Sato,Abdulghani Kohilan,Marwan K. Tayeh,Shan Chen,Suzanne M. Leal,Mahmoud Al-Salem,Hatem El‐Shanti	2009	101
14	Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications Genetics in Medicine ·Marwan K. Tayeh,Ephrem Chin,Vanessa Rangel Miller,Lora Jh Bean,Bradford Coffee,Madhuri Hegde	2009	32
15	Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning Human Molecular Genetics ·Marwan K. Tayeh,Hsan-Jan Yen,John S. Beck,Charles Searby,Trudi A. Westfall,Hilary Griesbach,Val C. Sheffield,Diane C. Slusarski	2008	58
16	Bardet–Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function Human Molecular Genetics ·Hsan-Jan Yen,Marwan K. Tayeh,Robert F. Mullins,Edwin M. Stone,Val C. Sheffield,Diane C. Slusarski	2006	144
17	Homozygosity mapping with SNP arrays identifiesTRIM32, an E3 ubiquitin ligase, as a Bardet–Biedl syndrome gene (BBS11) Proceedings of the National Academy of Sciences ·Annie Chiang,John S. Beck,Hsan-Jan Yen,Marwan K. Tayeh,Todd E. Scheetz,Ruth E. Swiderski,Darryl Nishimura,Terry A. Braun,Kwang‐Youn A. Kim,Jian Huang,Khalil Elbedour,Rivka Carmi,Diane C. Slusarski,Thomas L. Casavant,Edwin M. Stone,Val C. Sheffield	2006	319
18	The Spectrum of Familial Mediterranean Fever Gene Mutations in Arabs: Report of a Large Series Seminars in Arthritis and Rheumatism ·Hasan A. Majeed,Mohammed El‐Khateeb,Hatem El‐Shanti,Zaid Abu Rabaiha,Marwan K. Tayeh,Dana A Najib	2005	61
19	Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome Human Molecular Genetics ·Melissa A. Fath,Robert F. Mullins,Charles Searby,Darryl Nishimura,Jun Wei,Kamal Rahmouni,Roger E. Davis,Marwan K. Tayeh,Michael Andrews,Baoli Yang,Curt D. Sigmund,Edwin M. Stone,Val C. Sheffield	2005	148
20	Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population. PubMed ·Jamil Al-Alami,Marwan K. Tayeh,Dana A Najib,Ziad A Abu-Rubaiha,Hassan A. Majeed,Mohammed S. Al-Khateeb,Hatem El‐Shanti	2003	49

About Marwan K. Tayeh

Marwan K. Tayeh is a scholar working on Genetics, Molecular Biology and Pharmacology, having authored 26 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (8 papers), Genomic variations and chromosomal abnormalities (5 papers), Nuclear Structure and Function (4 papers), Genetic and Kidney Cyst Diseases (4 papers), Genomics and Rare Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers), Congenital heart defects research (3 papers) and Inflammasome and immune disorders (3 papers). The work is most often cited by research in Genetics (694 citations), Molecular Biology (828 citations) and Statistics and Probability (65 citations). Marwan K. Tayeh has collaborated with scholars based in United States, Jordan and Türkiye. Frequent co-authors include Val C. Sheffield, Edwin M. Stone, Diane C. Slusarski, Robert F. Mullins, Hatem El‐Shanti, Darryl Nishimura, John S. Beck, Khalil Elbedour, Todd E. Scheetz and Ruth E. Swiderski. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Blood.

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