Daouk, Ghaleb
eCommons Login: GHD2
first name: Ghaleb
last name: Daouk
coauthor of: Hildebrandt, Friedhelm
coauthor of: Daga, Ankana
coauthor of: Somers, Michael
coauthor of: Ingelfinger, Julie
coauthor of: Baum, Michelle
full name: Ghaleb Hassan Daouk, M.D.
has faculty rank: Assistant Professor
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latitude: 42.33743600000000
longitude: -71.10544700000000
Person ID: 2855
person in primary position: Assistant Professor of Pediatrics
physical neighbor: Baum, Michelle
physical neighbor: Briscoe, David
physical neighbor: Ferguson, Michael
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physical neighbor: Rodig, Nancy
similar to: Hildebrandt, Friedhelm
similar to: Alkuraya, Fowzan
similar to: Chung, Wendy
similar to: Nelson, Caleb
similar to: Chow, Jeanne
type: Agent
type: Person
selected publications: Authorship 1748492
selected publications: Authorship 1419049
selected publications: Authorship 1299035
selected publications: Authorship 1284007
selected publications: Authorship 1051169
selected publications: Authorship 1124100
selected publications: Authorship 1089617
selected publications: Authorship 1067895
selected publications: Authorship 1045710
selected publications: Authorship 1025794
selected publications: Authorship 1011561
selected publications: Authorship 1012077
selected publications: Authorship 946453
selected publications: Authorship 516420
selected publications: Authorship 215864
selected publications: Authorship 430789
selected publications: Authorship 549614
selected publications: Authorship 6231
selected publications: Authorship 196209
selected publications: Authorship 500740
selected publications: Authorship 332963
selected publications: Authorship 279086
selected publications: Authorship 191072
research areas: Urogenital Abnormalities
research areas: Vesico-Ureteral Reflux
research areas: Urinary Tract
research areas: Nephrotic Syndrome
research areas: Pedigree
mailing address: 300 Longwood Ave
middle name or initial: Hassan
positions: Assistant Professor of Pediatrics
phone: 617/726-5642
preferred title: Assistant Professor of Pediatrics

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Authorship 1045710
type: Authorship
author rank in publication: 13
linked author: Daouk, Ghaleb
linked information resource: Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome.

Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome.
PubMed Identifier: 29483232
author list: Warejko JK, Schueler M, Vivante A, Tan W, Daga A, Lawson JA, Braun DA, Shril S, Amann K, Somers MJG, Rodig NM, Baum MA, Daouk G, Traum AZ, Kim HB, Vakili K, Porras D, Lock J, Rivkin MJ, Chaudry G, Smoot LB, Singh MN, Smith ER, Mane SM, Lifton RP, Stein DR, Ferguson MA, Hildebrandt F
published in: Hypertension (Dallas, Tex. : 1979)
information resource reference: Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ˜43% of 35 Families With Midaortic Syndrome. Hypertension. 2018 04; 71(4):691-699.
journal title abbreviation: Hypertension
publication date: 2018-02-26T00:00:00
year: 2018
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1051169
type: Authorship
author rank in publication: 20
linked author: Daouk, Ghaleb
linked information resource: Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.

Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
PubMed Identifier: 29534211
author list: Braun DA, Warejko JK, Ashraf S, Tan W, Daga A, Schneider R, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Nakayama M, Schapiro D, Rao J, Schmidt JM, Hoogstraten CA, Hugo H, Bakkaloglu SA, Kari JA, El Desoky S, Daouk G, Mane S, Lifton RP, Shril S, Hildebrandt F
published in: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
information resource reference: Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome. Nephrol Dial Transplant. 2019 03 01; 34(3):485-493.
journal title abbreviation: Nephrol Dial Transplant
publication date: 2019-03-01T00:00:00
year: 2019
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1067895
type: Authorship
author rank in publication: 14
linked author: Daouk, Ghaleb
linked information resource: A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes.

A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes.
PubMed Identifier: 29791858
author list: Rinschen MM, Gödel M, Grahammer F, Zschiedrich S, Helmstädter M, Kretz O, Zarei M, Braun DA, Dittrich S, Pahmeyer C, Schroder P, Teetzen C, Gee H, Daouk G, Pohl M, Kuhn E, Schermer B, Küttner V, Boerries M, Busch H, Schiffer M, Bergmann C, Krüger M, Hildebrandt F, Dengjel J, Benzing T, Huber TB
published in: Cell reports
information resource reference: A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes. Cell Rep. 2018 05 22; 23(8):2495-2508.
journal title abbreviation: Cell Rep
publication date: 2018-05-22T00:00:00
year: 2018
type: Academic Article
type: Article
type: Document
type: Information Resource

Tuberous sclerosis complex and renal angiomyolipoma: case report and review of the literature.
PubMed Identifier: 16791610
author list: Winterkorn EB, Daouk GH, Anupindi S, Thiele EA
published in: Pediatric nephrology (Berlin, Germany)
information resource reference: Tuberous sclerosis complex and renal angiomyolipoma: case report and review of the literature. Pediatr Nephrol. 2006 Aug; 21(8):1189-93.
journal title abbreviation: Pediatr Nephrol
publication date: 2006-06-22T00:00:00
year: 2006
type: Academic Article
type: Article
type: Document
type: Information Resource

Induction of a cellular enzyme for energy metabolism by transforming domains of adenovirus E1a.
PubMed Identifier: 2138706
author list: Kaddurah-Daouk R, Lillie JW, Daouk GH, Green MR, Kingston R, Schimmel P
published in: Molecular and cellular biology
information resource reference: Induction of a cellular enzyme for energy metabolism by transforming domains of adenovirus E1a. Mol Cell Biol. 1990 Apr; 10(4):1476-83.
journal title abbreviation: Mol Cell Biol
publication date: 1990-04-01T00:00:00
year: 1990
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1089617
type: Authorship
author rank in publication: 37
linked author: Daouk, Ghaleb
linked information resource: Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
PubMed Identifier: 30143558
author list: van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanovic R, Stajic N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F
published in: Journal of the American Society of Nephrology : JASN
information resource reference: Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. J Am Soc Nephrol. 2018 09; 29(9):2348-2361.
journal title abbreviation: J Am Soc Nephrol
publication date: 2018-08-24T00:00:00
year: 2018
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1124100
type: Authorship
author rank in publication: 29
linked author: Daouk, Ghaleb
linked information resource: Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
PubMed Identifier: 30655312
author list: Mann N, Braun DA, Amann K, Tan W, Shril S, Connaughton DM, Nakayama M, Schneider R, Kitzler TM, van der Ven AT, Chen J, Ityel H, Vivante A, Majmundar AJ, Daga A, Warejko JK, Lovric S, Ashraf S, Jobst-Schwan T, Widmeier E, Hugo H, Mane SM, Spaneas L, Somers MJG, Ferguson MA, Traum AZ, Stein DR, Baum MA, Daouk GH, Lifton RP, Manzi S, Vakili K, Kim HB, Rodig NM, Hildebrandt F
published in: Journal of the American Society of Nephrology : JASN
information resource reference: Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients. J Am Soc Nephrol. 2019 02; 30(2):201-215.
journal title abbreviation: J Am Soc Nephrol
publication date: 2019-01-17T00:00:00
year: 2019
type: Academic Article
type: Article
type: Document
type: Information Resource

Regulation of coenzyme utilization by the dual nucleotide-specific glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroids.
PubMed Identifier: 42353
author list: Levy HR, Daouk GH, Katopes MA
published in: Archives of biochemistry and biophysics
information resource reference: Regulation of coenzyme utilization by the dual nucleotide-specific glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroids. Arch Biochem Biophys. 1979 Dec; 198(2):406-13.
journal title abbreviation: Arch Biochem Biophys
publication date: 1979-12-01T00:00:00
year: 1979
type: Academic Article
type: Article
type: Document
type: Information Resource

Inhibition of proteinase 3 by ANCA and its correlation with disease activity in Wegener's granulomatosis.
PubMed Identifier: 7643521
author list: Daouk GH, Palsson R, Arnaout MA
published in: Kidney international
information resource reference: Inhibition of proteinase 3 by ANCA and its correlation with disease activity in Wegener's granulomatosis. Kidney Int. 1995 Jun; 47(6):1528-36.
journal title abbreviation: Kidney Int
publication date: 1995-06-01T00:00:00
year: 1995
type: Academic Article
type: Article
type: Document
type: Information Resource

Nephrotic Syndrome
MeSH DescriptorUI: D009404
MeSH semantic group name: Disorders
number of authors: 133
number of publications: 412
uniqueness weight: 0.725602
type: Concept

Urinary Tract
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MeSH semantic group name: Anatomy
number of authors: 151
number of publications: 305
uniqueness weight: 0.771165
type: Concept

Vesico-Ureteral Reflux
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number of authors: 113
number of publications: 444
uniqueness weight: 0.739972
type: Concept

Pedigree
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MeSH semantic group name: Concepts & Ideas
number of authors: 1248
number of publications: 4620
uniqueness weight: 0.563303
type: Concept

Urogenital Abnormalities
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number of authors: 131
number of publications: 257
uniqueness weight: 0.789273
type: Concept

Pediatrics
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Radiology
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Surgery
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Nephrology
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Urology
type: Division
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Genetics
type: Division
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Boston Children's Hospital
type: Organization

Massachusetts General Hospital
type: Organization

Briscoe, David
eCommons Login: DMB5
first name: David
last name: Briscoe
full name: David Michael Briscoe, M.B.,B.Ch.
has faculty rank: Full Professor
latitude: 42.33743600000000
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Person ID: 39352
person in primary position: Professor of Pediatrics
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Somers, Michael
eCommons Login: MJS4
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has faculty rank: Associate Professor
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Person ID: 21024
person in primary position: Associate Professor of Pediatrics
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Ferguson, Michael
eCommons Login: MAF23
first name: Michael
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Person ID: 77133
person in primary position: Assistant Professor of Pediatrics
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Nelson, Caleb
eCommons Login: CPN4
first name: Caleb
last name: Nelson
full name: Caleb Nelson, M.D.
has faculty rank: Associate Professor
latitude: 42.33743600000000
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Person ID: 41242
person in primary position: Associate Professor of Surgery
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preferred title: Associate Professor of Surgery

Rodig, Nancy
eCommons Login: NMR1
first name: Nancy
last name: Rodig
full name: Nancy MacDonald Rodig, M.D.
has faculty rank: Assistant Professor
latitude: 42.33743600000000
longitude: -71.10544700000000
Person ID: 44457
person in primary position: Assistant Professor of Pediatrics
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Ingelfinger, Julie
eCommons Login: JRI1
first name: Julie
last name: Ingelfinger
full name: Julie Rich Ingelfinger, M.D.
has faculty rank: Full Professor
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person in primary position: Professor of Pediatrics
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Baum, Michelle
eCommons Login: MAB7
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has faculty rank: Associate Professor
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Person ID: 2274
person in primary position: Associate Professor of Pediatrics
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Alkuraya, Fowzan
eCommons Login: FSA2
first name: Fowzan
last name: Alkuraya
full name: Fowzan Sami Alkuraya, M.B.,B.S.
has faculty rank: Instructor
latitude: 42.33837200000000
longitude: -71.10326900000000
Person ID: 41121
person in primary position: Instructor in Pediatrics
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preferred title: Instructor in Pediatrics

Hildebrandt, Friedhelm
eCommons Login: FH61
first name: Friedhelm
last name: Hildebrandt
full name: Friedhelm Hildebrandt, M.D.
has faculty rank: Full Professor
Person ID: 110331
person in primary position: William E. Harmon Professor of Pediatrics Nephrology
type: Agent
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preferred title: William E. Harmon Professor of Pediatrics Nephrology

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Chow, Jeanne
eCommons Login: JSC8
first name: Jeanne
last name: Chow
full name: Jeanne San-Yu Chow, M.D.
has faculty rank: Associate Professor
latitude: 42.33743600000000
longitude: -71.10544700000000
Person ID: 67176
person in primary position: Associate Professor of Radiology
type: Agent
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preferred title: Associate Professor of Radiology

Pal, Soumitro
eCommons Login: SP15
first name: Soumitro
last name: Pal
full name: Soumitro Pal, Ph.D.
has faculty rank: Associate Professor
latitude: 42.33743600000000
longitude: -71.10544700000000
photo: https://connects.catalyst.harvard.edu/Profiles/profile/Modules/CustomViewPersonGeneralInfo/PhotoHandler.ashx
Person ID: 13192
person in primary position: Associate Professor of Pediatrics
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Authorship 1284007
type: Authorship
author rank in publication: 73
linked author: Daouk, Ghaleb
linked information resource: Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
PubMed Identifier: 32891193
author list: Connaughton DM, Dai R, Owen DJ, Marquez J, Mann N, Graham-Paquin AL, Nakayama M, Coyaud E, Laurent EMN, St-Germain JR, Blok LS, Vino A, Klämbt V, Deutsch K, Wu CW, Kolvenbach CM, Kause F, Ottlewski I, Schneider R, Kitzler TM, Majmundar AJ, Buerger F, Onuchic-Whitford AC, Youying M, Kolb A, Salmanullah D, Chen E, van der Ven AT, Rao J, Ityel H, Seltzsam S, Rieke JM, Chen J, Vivante A, Hwang DY, Kohl S, Dworschak GC, Hermle T, Alders M, Bartolomaeus T, Bauer SB, Baum MA, Brilstra EH, Challman TD, Zyskind J, Costin CE, Dipple KM, Duijkers FA, Ferguson M, Fitzpatrick DR, Fick R, Glass IA, Hulick PJ, Kline AD, Krey I, Kumar S, Lu W, Marco EJ, Wentzensen IM, Mefford HC, Platzer K, Povolotskaya IS, Savatt JM, Shcherbakova NV, Senguttuvan P, Squire AE, Stein DR, Thiffault I, Voinova VY, Somers MJG, Ferguson MA, Traum AZ, Daouk GH, Daga A, Rodig NM, Terhal PA, van Binsbergen E, Eid LA, Tasic V, Rasouly HM, Lim TY, Ahram DF, Gharavi AG, Reutter HM, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Lifton RP, Xu H, Mane SM, Sanna-Cherchi S, Sharrocks AD, Raught B, Fisher SE, Bouchard M, Khokha MK, Shril S, Hildebrandt F
published in: American journal of human genetics
information resource reference: Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations. Am J Hum Genet. 2020 10 01; 107(4):727-742.
journal title abbreviation: Am J Hum Genet
publication date: 2020-09-04T00:00:00
year: 2020
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1299035
type: Authorship
author rank in publication: 3
linked author: Daouk, Ghaleb
linked information resource: Beyond the tubule: pathological variants of LRP2, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease.

Beyond the tubule: pathological variants of LRP2, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease.
PubMed Identifier: 33103447
author list: Charlton JR, Tan W, Daouk G, Teot L, Rosen S, Bennett KM, Cwiek A, Nam S, Emma F, Jouret F, Oliveira JP, Tranebjærg L, Frykholm C, Mane S, Hildebrandt F, Srivastava T, Storm T, Christensen EI, Nielsen R
published in: American journal of physiology. Renal physiology
information resource reference: Beyond the tubule: pathological variants of LRP2, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease. Am J Physiol Renal Physiol. 2020 12 01; 319(6):F988-F999.
journal title abbreviation: Am J Physiol Renal Physiol
publication date: 2020-10-26T00:00:00
year: 2020
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 196209
type: Authorship
author rank in publication: 5
linked author: Daouk, Ghaleb
linked information resource: Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination.

Authorship 1419049
type: Authorship
author rank in publication: 33
linked author: Daouk, Ghaleb
linked information resource: Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
PubMed Identifier: 34906515
author list: Seltzsam S, Wang C, Zheng B, Mann N, Connaughton DM, Wu CW, Schneider S, Schierbaum L, Kause F, Kolvenbach CM, Nakayama M, Dai R, Ottlewski I, Schneider R, Deutsch K, Buerger F, Klämbt V, Mao Y, Onuchic-Whitford AC, Nicolas-Frank C, Yousef K, Pantel D, Lai EW, Salmanullah D, Majmundar AJ, Bauer SB, Rodig NM, Somers MJG, Traum AZ, Stein DR, Daga A, Baum MA, Daouk GH, Tasic V, Awad HS, Eid LA, El Desoky S, Shalaby M, Kari JA, Fathy HM, Soliman NA, Mane SM, Shril S, Ferguson MA, Hildebrandt F
published in: Genetics in medicine : official journal of the American College of Medical Genetics
information resource reference: Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT. Genet Med. 2022 02; 24(2):307-318.
journal title abbreviation: Genet Med
publication date: 2021-11-30T00:00:00
year: 2021
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 191072
type: Authorship
author rank in publication: 2
linked author: Daouk, Ghaleb
linked information resource: Simultaneous analysis of NAD- and NADP-linked activities of dual nucleotide-specific dehydrogenases. Application to Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase.

Authorship 215864
type: Authorship
author rank in publication: 2
linked author: Daouk, Ghaleb
linked information resource: Tuberous sclerosis complex and renal angiomyolipoma: case report and review of the literature.

Chung, Wendy
eCommons Login: wec138
first name: Wendy
last name: Chung
full name: Wendy Chung, M.D., Ph.D.
has faculty rank: Full Professor
Person ID: 214837
person in primary position: Mary Ellen Avery Professor of Pediatrics
type: Agent
type: Person
preferred title: Mary Ellen Avery Professor of Pediatrics

Authorship 516420
type: Authorship
author rank in publication: 1
linked author: Daouk, Ghaleb
linked information resource: Recent advances in the pathogenesis of hypertension in children.

Authorship 549614
type: Authorship
author rank in publication: 2
linked author: Daouk, Ghaleb
linked information resource: Postnatal transient renal insufficiency in the feto-fetal transfusion syndrome.

Authorship 1748492
type: Authorship
author rank in publication: 38
linked author: Daouk, Ghaleb
linked information resource: Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
PubMed Identifier: 40223730
author list: Merz LM, Kolvenbach CM, Wang C, Mertens ND, Seltzsam S, Mansour B, Zheng B, Schneider S, Schierbaum L, Hölzel S, Salmanullah D, Pantel D, Kalkar G, Connaughton DM, Mann N, Wu CW, Kause F, Nakayama M, Dai R, Schneider R, Buerger F, Nicolas-Frank C, Yousef K, Lemberg K, Saida K, Yu S, Elmubarak I, Franken GAC, Lomjansook K, Braun A, Bauer SB, Rodig NM, Somers MJG, Traum AZ, Stein DR, Daga A, Baum MA, Daouk GH, Awad HS, Eid LA, El Desoky S, Shalaby MA, Kari JA, Ooda S, Fathy HM, Soliman NA, Nabhan M, Abdelrahman S, Hilger AC, Mane SM, Ferguson MA, Tasic V, Shril S, Hildebrandt F
published in: Genetics in medicine : official journal of the American College of Medical Genetics
information resource reference: Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families. Genet Med. 2025 Jul; 27(7):101432.
journal title abbreviation: Genet Med
publication date: 2025-04-11T00:00:00
year: 2025
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 430789
type: Authorship
author rank in publication: 2
linked author: Daouk, Ghaleb
linked information resource: Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 11-2004. A boy with rash, edema, and hypertension.

General Pediatrics
type: Division
type: Organization

Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Professor of Pediatrics
position in organization: Massachusetts General Hospital

Mary Ellen Avery Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: General Pediatrics
sort order: 1
type: Position
HR job title: Mary Ellen Avery Professor of Pediatrics
position in organization: Boston Children's Hospital

Associate Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Associate Professor of Pediatrics
position in organization: Boston Children's Hospital

Assistant Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Assistant Professor of Pediatrics
position in organization: Boston Children's Hospital

Associate Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Associate Professor of Pediatrics
position in organization: Boston Children's Hospital

Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Professor of Pediatrics
position in organization: Boston Children's Hospital

Assistant Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Assistant Professor of Pediatrics
position in organization: Boston Children's Hospital

Assistant Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Assistant Professor of Pediatrics
position in organization: Boston Children's Hospital

William E. Harmon Professor of Pediatrics Nephrology
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: William E. Harmon Professor of Pediatrics Nephrology
position in organization: Boston Children's Hospital

Associate Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Associate Professor of Pediatrics
position in organization: Boston Children's Hospital

Associate Professor of Surgery
is primary position: true
position in department: Surgery
position in division: Urology
sort order: 1
type: Position
HR job title: Associate Professor of Surgery
position in organization: Boston Children's Hospital

Instructor in Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Genetics
sort order: 1
type: Position
HR job title: Instructor in Pediatrics
position in organization: Boston Children's Hospital

Assistant Professor of Pediatrics
is primary position: true
position in department: Pediatrics
position in division: Nephrology
sort order: 1
type: Position
HR job title: Assistant Professor of Pediatrics
position in organization: Boston Children's Hospital

Associate Professor of Radiology
is primary position: true
position in department: Radiology
position in division: https://connects.catalyst.harvard.edu/Profiles/profile/1229413
sort order: 1
type: Position
HR job title: Associate Professor of Radiology
position in organization: Boston Children's Hospital

Authorship 279086
type: Authorship
author rank in publication: 2
linked author: Daouk, Ghaleb
linked information resource: Regulation of coenzyme utilization by the dual nucleotide-specific glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroids.

Daga, Ankana
eCommons Login: AD306
first name: Ankana
last name: Daga
full name: Ankana Daga, M.D.
has faculty rank: Assistant Professor
Person ID: 141972
person in primary position: Assistant Professor of Pediatrics
type: Agent
type: Person
preferred title: Assistant Professor of Pediatrics

Authorship 6231
type: Authorship
author rank in publication: 1
linked author: Daouk, Ghaleb
linked information resource: Inhibition of proteinase 3 by ANCA and its correlation with disease activity in Wegener's granulomatosis.

Assistant Professor
sort order: 2
type: Faculty Rank

Associate Professor
sort order: 1
type: Faculty Rank

Full Professor
sort order: 0
type: Faculty Rank

Instructor
sort order: 4
type: Faculty Rank

Authorship 500740
type: Authorship
author rank in publication: 3
linked author: Daouk, Ghaleb
linked information resource: Induction of a cellular enzyme for energy metabolism by transforming domains of adenovirus E1a.

Authorship 332963
type: Authorship
author rank in publication: 1
linked author: Daouk, Ghaleb
linked information resource: Isolation of a functional human gene for brain creatine kinase.

Authorship 946453
type: Authorship
author rank in publication: 8
linked author: Daouk, Ghaleb
linked information resource: Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.

Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
PubMed Identifier: 27151922
author list: Vivante A, Hwang DY, Kohl S, Chen J, Shril S, Schulz J, van der Ven A, Daouk G, Soliman NA, Kumar AS, Senguttuvan P, Kehinde EO, Tasic V, Hildebrandt F
published in: Journal of the American Society of Nephrology : JASN
information resource reference: Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract. J Am Soc Nephrol. 2017 Jan; 28(1):69-75.
journal title abbreviation: J Am Soc Nephrol
publication date: 2016-05-05T00:00:00
year: 2016
type: Academic Article
type: Article
type: Document
type: Information Resource

Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination.
PubMed Identifier: 1674725
author list: Benger JC, Teshima I, Walter MA, Brubacher MG, Daouk GH, Cox DW
published in: Genomics
information resource reference: Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombination. Genomics. 1991 Apr; 9(4):614-22.
journal title abbreviation: Genomics
publication date: 1991-04-01T00:00:00
year: 1991
type: Academic Article
type: Article
type: Document
type: Information Resource

Isolation of a functional human gene for brain creatine kinase.
PubMed Identifier: 2828370
author list: Daouk GH, Kaddurah-Daouk R, Putney S, Kingston R, Schimmel P
published in: The Journal of biological chemistry
information resource reference: Isolation of a functional human gene for brain creatine kinase. J Biol Chem. 1988 Feb 15; 263(5):2442-6.
journal title abbreviation: J Biol Chem
publication date: 1988-02-15T00:00:00
year: 1988
type: Academic Article
type: Article
type: Document
type: Information Resource

Postnatal transient renal insufficiency in the feto-fetal transfusion syndrome.
PubMed Identifier: 10228996
author list: Christensen AM, Daouk GH, Norling LL, Catlin EA, Ingelfinger JR
published in: Pediatric nephrology (Berlin, Germany)
information resource reference: Postnatal transient renal insufficiency in the feto-fetal transfusion syndrome. Pediatr Nephrol. 1999 Feb; 13(2):117-20.
journal title abbreviation: Pediatr Nephrol
publication date: 1999-02-01T00:00:00
year: 1999
type: Academic Article
type: Article
type: Document
type: Information Resource

Recent advances in the pathogenesis of hypertension in children.
PubMed Identifier: 21462841
author list: Daouk GH, Ingelfinger JR
published in: Le Journal medical libanais. The Lebanese medical journal
information resource reference: Recent advances in the pathogenesis of hypertension in children. J Med Liban. 2010 Jul-Sep; 58(3):137-41.
journal title abbreviation: J Med Liban
publication date: 2010-07-01T00:00:00
year: 2010
type: Academic Article
type: Article
type: Document
type: Information Resource

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.
PubMed Identifier: 28893421
author list: Daga A, Majmundar AJ, Braun DA, Gee HY, Lawson JA, Shril S, Jobst-Schwan T, Vivante A, Schapiro D, Tan W, Warejko JK, Widmeier E, Nelson CP, Fathy HM, Gucev Z, Soliman NA, Hashmi S, Halbritter J, Halty M, Kari JA, El-Desoky S, Ferguson MA, Somers MJG, Traum AZ, Stein DR, Daouk GH, Rodig NM, Katz A, Hanna C, Schwaderer AL, Sayer JA, Wassner AJ, Mane S, Lifton RP, Milosevic D, Tasic V, Baum MA, Hildebrandt F
published in: Kidney international
information resource reference: Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. Kidney Int. 2018 01; 93(1):204-213.
journal title abbreviation: Kidney Int
publication date: 2017-10-12T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1011561
type: Authorship
author rank in publication: 26
linked author: Daouk, Ghaleb
linked information resource: Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.

Authorship 1012077
type: Authorship
author rank in publication: 10
linked author: Daouk, Ghaleb
linked information resource: Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.

Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.
PubMed Identifier: 28921387
author list: Tan W, Lovric S, Ashraf S, Rao J, Schapiro D, Airik M, Shril S, Gee HY, Baum M, Daouk G, Ferguson MA, Rodig N, Somers MJG, Stein DR, Vivante A, Warejko JK, Widmeier E, Hildebrandt F
published in: Pediatric nephrology (Berlin, Germany)
information resource reference: Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center. Pediatr Nephrol. 2018 02; 33(2):305-314.
journal title abbreviation: Pediatr Nephrol
publication date: 2017-09-18T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 11-2004. A boy with rash, edema, and hypertension.
PubMed Identifier: 15071130
author list: Somers MJ, Daouk GH, McCluskey RT
published in: The New England journal of medicine
information resource reference: Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 11-2004. A boy with rash, edema, and hypertension. N Engl J Med. 2004 Apr 08; 350(15):1550-9.
journal title abbreviation: N Engl J Med
publication date: 2004-04-08T00:00:00
year: 2004
type: Academic Article
type: Article
type: Document
type: Information Resource

Simultaneous analysis of NAD- and NADP-linked activities of dual nucleotide-specific dehydrogenases. Application to Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase.
PubMed Identifier: 35541
author list: Levy HR, Daouk GH
published in: The Journal of biological chemistry
information resource reference: Simultaneous analysis of NAD- and NADP-linked activities of dual nucleotide-specific dehydrogenases. Application to Leuconostoc mesenteroides glucose-6-phosphate dehydrogenase. J Biol Chem. 1979 Jun 10; 254(11):4843-7.
journal title abbreviation: J Biol Chem
publication date: 1979-06-10T00:00:00
year: 1979
type: Academic Article
type: Article
type: Document
type: Information Resource

Authorship 1025794
type: Authorship
author rank in publication: 27
linked author: Daouk, Ghaleb
linked information resource: Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
PubMed Identifier: 29127259
author list: Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, Ashraf S, Rao J, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Schneider R, Gee HY, Schmidt JM, Vivante A, van der Ven AT, Ityel H, Chen J, Sadowski CE, Kohl S, Pabst WL, Nakayama M, Somers MJG, Rodig NM, Daouk G, Baum M, Stein DR, Ferguson MA, Traum AZ, Soliman NA, Kari JA, El Desoky S, Fathy H, Zenker M, Bakkaloglu SA, Müller D, Noyan A, Ozaltin F, Cadnapaphornchai MA, Hashmi S, Hopcian J, Kopp JB, Benador N, Bockenhauer D, Bogdanovic R, Stajic N, Chernin G, Ettenger R, Fehrenbach H, Kemper M, Munarriz RL, Podracka L, Büscher R, Serdaroglu E, Tasic V, Mane S, Lifton RP, Braun DA, Hildebrandt F
published in: Clinical journal of the American Society of Nephrology : CJASN
information resource reference: Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome. Clin J Am Soc Nephrol. 2018 01 06; 13(1):53-62.
journal title abbreviation: Clin J Am Soc Nephrol
publication date: 2017-11-10T00:00:00
year: 2017
type: Academic Article
type: Article
type: Document
type: Information Resource

300 Longwood Ave
type: Address
address line 1: Childrens Hospital
address line 2: Pediatric Nephrology - Hunn 3
address line 3: 300 Longwood Ave
city: Boston
postal code: 02115
state or province: MA