Sharon F. Suchy

3.3k citations

31 papers · 1.5k indexed · h-index 17

Cell Biology top 1%
- Cellular transport and secretion 13
- Biotin and Related Studies 3
Molecular Biology top 10%
- Glycosylation and Glycoproteins Research 3
- Protein Kinase Regulation and GTPase Signaling 3
Pathology and Forensic Medicine top 10%
- Biomedical Research and Pathophysiology 3
Physiology top 5%
Genetics top 10%
- Genomics and Rare Diseases 3
Clinical Biochemistry
- Metabolism and Genetic Disorders 4
Surgery
- Pancreatic function and diabetes 4

Co-authors: Robert L. Nussbaum Isabelle Olivos‐Glander Pietro De Camilli Gary W. Cline Anthony J. Romanelli Markus R. Wenk Louise Lucast David J. Bernard
Cited by: Cell Biology Molecular Biology Pathology and Forensic Medicine
Journals: The American Journal of Human Genetics (4 papers)Molecular Genetics and Metabolism (3 papers)Genetics in Medicine (2 papers)
Partner nations: United States Canada Saudi Arabia

In The Last Decade

Sharon F. Suchy

30 papers receiving 1.5k citations

Peers

Countries citing papers authored by Sharon F. Suchy

Since Specialization

Citations

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

Fields of papers citing papers by Sharon F. Suchy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sharon F. Suchy. 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 Sharon F. Suchy. The network helps show where Sharon F. Suchy may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Evaluating the strength of evidence for genes implicated in peroxisomal disorders using the ClinGen clinical validity framework and providing updates to the peroxisomal disease nomenclature Molecular Genetics and Metabolism ·Shruthi Mohan,Lian-Xian Han,Meredith Weaver,U. Kanani,Irene De Biase,Jennifer Goldstein,Rong Mao,Jennifer McGlaughon,Ann B. Moser,Aurora Pujol,Sharon F. Suchy,Tatiana Yuzyuk,Nancy Braverman	2023	0
2	Interference of nuclear mitochondrial DNA segments in mitochondrial DNA testing resembles biparental transmission of mitochondrial DNA in humans Genetics in Medicine ·Shokhista Mustanova,Hong Cui,Joseph M. Devaney,Hannes Veinla,Iveta Elksne,Xinyue Liu,Rhonda E. Schnur,裕史坂巻,Ariel Brautbar,Juvianee Estrada‐Veras,Kelvin Wamalwa,Allyn McConkie‐Rosell,Marie McDonald,Benjamin D. Solomon,Sean Hofherr,Gabriele Richard,Sharon F. Suchy	2021	9
3	Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation The American Journal of Human Genetics ·Bobby G. Ng,Gege Xu,J. De Oliveira Leite,昭吾柳澤,Deepali N. Shinde,Kelly Radtke,Kimiyo Raymond,Carlito B. Lebrilla,Ali Alasmari,Sharon F. Suchy,Zöe Powis,Eissa Faqeih,Susan A. Berry,David F. Kronn,Hudson H. Freeze	2018	53
4	Comparison of the Diagnostic Yield of Comprehensive and Phenotypically Driven Multi-Gene Panels for Neuromuscular Disorders (P5.055) Neurology ·Amanda Lindy,Francesca Marverti,Sharon F. Suchy,Dianalee McKnight	2016	1
5	First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children SHILAP Revista de lepidopterología ·Rufki Salihi,陈富志,Kirit Pindolia,Jithangi Wanigasinghe,Kristin G. Monaghan,Sharon F. Suchy,姬康飞,A.P. Kulik,Barry Wolf	2015	9
6	Novel large deletion in the ACTA1 gene in a child with autosomal recessive nemaline myopathy Neuromuscular Disorders ·Bethany Friedman,M. Sharif,Carolina Tesi Rocha,Delu Zhou,Cheryl A. Palmer,Sharon F. Suchy	2013	3
7	Exon-level array CGH in a large clinical cohort demonstrates increased sensitivity of diagnostic testing for Mendelian disorders Genetics in Medicine ·Swaroop Aradhya,Rachel Lewis,Mark Russell,Nina Breunig,Amanda Stafford,Barbara A. Boggs,Kathleen S. Hruska,Nizar Smaoui,John G. Compton,Gabriele Richard,Sharon F. Suchy	2012	48
8	The effect of missense mutations in the RhoGAP-homology domain on ocrl1 function Molecular Genetics and Metabolism ·Uta Lichter‐Konecki,R. Couch,Ogün PEÇENEK,Sharon F. Suchy,Robert L. Nussbaum	2006	41
9	Dent Disease with Mutations in OCRL1 The American Journal of Human Genetics ·R R Hoopes,Antony E. Shrimpton,Stephen J. Knohl,Paul Hueber,Bernd Höppe,János Mátyus,Ari M. Simckes,Velibor Tasic,Burkhard Toenshoff,Sharon F. Suchy,Robert L. Nussbaum,Steven J. Scheinman	2005	247
10	Phosphoinositide profiling in complex lipid mixtures using electrospray ionization mass spectrometry Nature Biotechnology ·Markus R. Wenk,Louise Lucast,Gilbert Di Paolo,Anthony J. Romanelli,Sharon F. Suchy,Robert L. Nussbaum,Gary W. Cline,Gerald I. Shulman,Walter J. McMurray,Pietro De Camilli	2003	216
11	The Deficiency of PIP2 5-Phosphatase in Lowe Syndrome Affects Actin Polymerization The American Journal of Human Genetics ·Sharon F. Suchy,Robert L. Nussbaum	2002	109
12	Sertoli Cell Vacuolization and Abnormal Germ Cell Adhesion in Mice Deficient in an Inositol Polyphosphate 5-Phosphatase1 Biology of Reproduction ·Elina Hellsten,David J. Bernard,Jennie W. Owens,Michael Eckhaus,Sharon F. Suchy,Robert L. Nussbaum	2002	41
13	Unusual renal features of Lowe syndrome in a mildly affected boy American Journal of Medical Genetics ·Andrea Gropman,Sondra W. Levin,Lynne Yao,Ti Lin,Sharon F. Suchy,Sharda G. Sabnis,Donald W. Hadley,Robert L. Nussbaum	2000	23
14	Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice. Journal of Clinical Investigation ·Pasi A. Jänne,Sharon F. Suchy,David J. Bernard,Marcy E. MacDonald,Jacqueline N. Crawley,Alexander Grinberg,Anthony Wynshaw‐Boris,H Westphal,Robert L. Nussbaum	1998	140
15	Mutations Are Not Uniformly Distributed throughout theOCRL1Gene in Lowe Syndrome Patients Molecular Genetics and Metabolism ·Quirós Lagares,Bonnie M. Orrison,Sharon F. Suchy,Richard A. Lewis,Robert L. Nussbaum	1998	42
16	Spectrum of Mutations in the OCRL1Gene in the Lowe Oculocerebrorenal Syndrome The American Journal of Human Genetics ·Ti Lin,Bonnie M. Orrison,Ummah Tafsirun,Sharon F. Suchy,Степанов Александр Владиславович,Richard A. Lewis,Robert L. Nussbaum	1997	80
17	False‐positive amniotic fluid acetylcholinesterase analysis in the third trimester Prenatal Diagnosis ·Sharon F. Suchy,G. Pa'l-Schmid	1993	1
18	The expression of a fucosyl-ganglioside in the molecular layer of the dentate gyrus following entorhinal cortical lesions Neuroscience Letters ·Sharon F. Suchy,Gerald A. Schwarting,Rona L. Gow,Julio J. Ramirez	1991	7
19	A monoclonal antibody, WCC4, recognizes a developmentally regulated ganglioside containing α-galactose and α-fucose present in the rat nervous system Brain Research ·Sharon F. Suchy,Miyuki Yamamoto,Luis A. Concha-Rebollar,Gerald A. Schwarting	1988	25
20	Amino Acids in Amniotic Fluid in the Second Trimester of Gestation Pediatric Research ·T. J. Deming,Sharon F. Suchy,Debra L. Weiner,Marcus Warner,David B. Flannery,Barry Wolf	1985	14

About Sharon F. Suchy

Sharon F. Suchy is a scholar working on Cell Biology, Clinical Biochemistry, Physiology, Molecular Biology and Pathology and Forensic Medicine, having authored 31 papers that have together received 1.5k indexed citations. Recurring topics across this work include Cellular transport and secretion (13 papers), Metabolism and Genetic Disorders (4 papers), Pancreatic function and diabetes (4 papers), Glycosylation and Glycoproteins Research (3 papers), Genomics and Rare Diseases (3 papers), Biomedical Research and Pathophysiology (3 papers), Biotin and Related Studies (3 papers) and Protein Kinase Regulation and GTPase Signaling (3 papers). The work is most often cited by research in Cell Biology (797 citations), Molecular Biology (946 citations), Pathology and Forensic Medicine (220 citations), Physiology (53 citations) and Genetics (270 citations). Sharon F. Suchy has collaborated with scholars based in United States, Canada and Saudi Arabia. Frequent co-authors include Robert L. Nussbaum, Isabelle Olivos‐Glander, Robert L. Nussbaum, Pietro De Camilli, Gary W. Cline, Anthony J. Romanelli, Markus R. Wenk, Louise Lucast, David J. Bernard and Walter J. McMurray. Their work appears in journals such as The American Journal of Human Genetics, Molecular Genetics and Metabolism, Genetics in Medicine, Neurology and Prenatal Diagnosis.

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