Shirlee Shril

5.2k total citations
36 papers, 505 citations indexed

About

Shirlee Shril is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Shirlee Shril has authored 36 papers receiving a total of 505 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 14 papers in Genetics and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Shirlee Shril's work include Renal and related cancers (20 papers), Renal Diseases and Glomerulopathies (10 papers) and Genetic and Kidney Cyst Diseases (8 papers). Shirlee Shril is often cited by papers focused on Renal and related cancers (20 papers), Renal Diseases and Glomerulopathies (10 papers) and Genetic and Kidney Cyst Diseases (8 papers). Shirlee Shril collaborates with scholars based in United States, Germany and Saudi Arabia. Shirlee Shril's co-authors include Friedhelm Hildebrandt, Daniela A. Braun, Velibor Tasić, Heon Yung Gee, Jan Halbritter, Caroline M. Kolvenbach, Asaf Vivante, John A. Sayer, Deborah R. Stein and Friedhelm Hildebrandt and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Shirlee Shril

28 papers receiving 498 citations

Peers

Countries citing papers authored by Shirlee Shril

Since Specialization

Citations

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

Fields of papers citing papers by Shirlee Shril

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shirlee Shril

This figure shows the co-authorship network connecting the top 25 collaborators of Shirlee Shril. A scholar is included among the top collaborators of Shirlee Shril 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 Shirlee Shril. Shirlee Shril 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	Pathogenic PHIP Variants are Variably Associated With CAKUT 2024 ·Kidney International Reports ·(unknown), (unknown), Ria Schönauer, (unknown), (unknown), (unknown), Georgia Vasileiou, (unknown), (unknown), Alma Kuechler, André Reis, Eva L. Decker, Carsten Bergmann, Konrad Platzer, Velibor Tasić, Karin M. Kirschner, Shirlee Shril, Friedhelm Hildebrandt, Wendy K. Chung, Jan Halbritter	3
2	Collaborative effort: managing Bardet-Biedl syndrome in pediatric patients. Case series and a literature review 2024 ·Frontiers in Endocrinology ·(unknown), (unknown), Agnieszka Tomaszewska, Friedhelm Hildebrandt, Thomas M. Kitzler, (unknown), (unknown), Shirlee Shril, Maria Szczepańska, Agnieszka Zachurzok	0
3	Genetic Contributions to Lower Urinary Tract Dysfunction 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Chunyan Wang, Ted Lee, (unknown), Mohamed Shalaby, Sherif El Desoky, Jameela A. Kari, Shirlee Shril, Friedhelm Hildebrandt, Nina Mann	0
4	Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney 2023 ·The Nephron journals/Nephron journals ·(unknown), (unknown), Florian Buerger, (unknown), (unknown), Chunyan Wang, Bixia Zheng, (unknown), Rufeng Dai, Dervla M. Connaughton, (unknown), Makiko Nakayama, Nina Mann, Shirlee Shril, Friedhelm Hildebrandt	0
5	Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life 2023 ·Acta Paediatrica ·(unknown), M. Thabet, (unknown), Ronen Schneider, Shirlee Shril, Florian Buerger, Friedhelm Hildebrandt, Hanan Fathy	2
6	The genetics and pathogenesis of CAKUT 2023 ·Nature Reviews Nephrology ·Caroline M. Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt	35
7	A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner 2022 ·The Journal of Clinical Endocrinology & Metabolism ·Reema L. Habiby, Daniel G. Bichet, Marie‐Françoise Arthus, (unknown), Shirlee Shril, Shrikant Mane, Amar J. Majmundar, Friedhelm Hildebrandt, Gary L. Robertson	0
8	A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families 2021 ·Human Mutation ·Eric Olinger, (unknown), (unknown), Issa Al Salmi, Elisa Molinari, Eissa Faqeih, Mohamed H. Al‐Hamed, (unknown), (unknown), Abdulrahman Al‐Hussaini, (unknown), Naif A. M. Almontashiri, Colin G. Miles, Shirlee Shril, Friedhelm Hildebrandt, Ian Wilson, John A. Sayer	9
9	Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia 2021 ·American Journal of Medical Genetics Part A ·Gabrielle Lemire, Bixia Zheng, (unknown), Ruobing Zou, (unknown), (unknown), Joseph de Nanassy, Bernard Lo, Chunyan Wang, Shirlee Shril, Sherif El Desoky, (unknown), Jameela A. Kari, Xueqi Wang, Kristin D. Kernohan, Kym M. Boycott, Friedhelm Hildebrandt, Sarah L. Sawyer	4
10	Sequencing the CaSR locus in Pakistani stone formers reveals a novel loss-of-function variant atypically associated with nephrolithiasis 2021 ·BMC Medical Genomics ·(unknown), (unknown), Wasim Shehzad, Amjad Riaz, (unknown), (unknown), (unknown), Shrikant Mane, Shirlee Shril, Friedhelm Hildebrandt, Muhammad Yasir Zahoor, Amar J. Majmundar	0
11	Whole-Exome Sequencing Identifies FOXL2, FOXA2, and FOXA3 as Candidate Genes for Monogenic Congenital Anomalies of the Kidneys and Urinary Tract 2021 ·Journal of the American Society of Nephrology ·Bixia Zheng, (unknown), Chunyan Wang, (unknown), (unknown), Dervla M. Connaughton, Nina Mann, Velibor Tasić, Shirlee Shril, Friedhelm Hildebrandt	1
12	Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitment 2020 ·Kidney International ·Ria Schönauer, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Daniela A. Braun, Shirlee Shril, Matthias Hansen, (unknown), Richard Sandford, Sophie Saunier, Alexandre Benmerah, Carsten Bergmann, Friedhelm Hildebrandt, Jan Halbritter	6
13	Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches 2020 ·Kidney International Reports ·Verena Klämbt, (unknown), Ronen Schneider, Florian Buerger, Hanan E. Shamseldin, (unknown), (unknown), Thomas M. Kitzler, Makiko Nakayama, Amar J. Majmundar, Nina Mann, Hannah Hugo, Eugen Widmeier, Weizhen Tan, Heidi L. Rehm, Shrikant Mane, Richard P. Lifton, Fowzan S. Alkuraya, Shirlee Shril, Friedhelm Hildebrandt	2
14	Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome 2019 ·Proceedings of the National Academy of Sciences ·(unknown), Peter E. Thelwall, Katrina Wood, Gavin J. Clowry, (unknown), Flora Silbermann, (unknown), Shirlee Shril, Elisa Molinari, Friedhelm Hildebrandt, Meral Gunay‐Aygun, Sophie Saunier, Heather J. Cordell, John A. Sayer, Colin G. Miles	20
15	Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature 2019 ·BMC Medical Genetics ·Ben Pode‐Shakked, Asaf Vivante, Ortal Barel, Shai Padeh, Dina Marek‐Yagel, (unknown), (unknown), Aviva Eliyahu, Irit Tirosh, (unknown), Shirlee Shril, Friedhelm Hildebrandt, Mordechai Shohat, Yair Anikster	13
16	Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy 2019 ·The American Journal of Human Genetics ·(unknown), Jan Halbritter, Daniela A. Braun, Markus Schueler, David Schapiro, John Hoon Rim, Sumeda Nandadasa, Won‐Il Choi, Eugen Widmeier, Shirlee Shril, Friederike Körber, Sidharth Kumar Sethi, Richard P. Lifton, Bodo B. Beck, Suneel Apte, Heon Yung Gee, Friedhelm Hildebrandt	31
17	Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis 2019 ·Human Genetics ·Ali Amar, Amar J. Majmundar, (unknown), Ayesha Afzal, Daniela A. Braun, Shirlee Shril, Ankana Daga, Tilman Jobst‐Schwan, Mumtaz Ahmad, John A. Sayer, Heon Yung Gee, Jan Halbritter, Thomas Knöpfel, Nati Hernando, Andreas Werner, Carsten A. Wagner, Shagufta Khaliq, Friedhelm Hildebrandt	35
18	Acute multi-sgRNA knockdown of KEOPS complex genes reproduces the microcephaly phenotype of the stable knockout zebrafish model 2018 ·PLoS ONE ·Tilman Jobst‐Schwan, Johanna Magdalena Schmidt, Ronen Schneider, Charlotte A. Hoogstraten, Jeremy F.P. Ullmann, David Schapiro, Amar J. Majmundar, (unknown), (unknown), Shirlee Shril, Daniela A. Braun, Annapurna Poduri, Friedhelm Hildebrandt	21
19	Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases 2017 ·Pediatric Nephrology ·Asaf Vivante, Hadas Ityel, Ben Pode‐Shakked, Jing Chen, Shirlee Shril, Amelie T. van der Ven, Nina Mann, Johanna Magdalena Schmidt, Reeval Segel, Adi Aran, Avraham Zeharia, Orna Staretz‐Chacham, Omer Bar‐Yosef, Annick Raas‐Rothschild, Yuval E. Landau, Richard P. Lifton, Yair Anikster, Friedhelm Hildebrandt	27
20	Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient with Syndromic CAKUT: A Case Report 2017 ·Molecular Syndromology ·Amelie T. van der Ven, Shirlee Shril, Hadas Ityel, Asaf Vivante, Jing Chen, Daw‐Yang Hwang, Kristen M. Laricchia, Monkol Lek, Velibor Tasić, Friedhelm Hildebrandt	5

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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